saramsey
commented
3 years ago This appears to have happened in commit 84c8d524b9d6cdd12bb6bd823abf30f8d8dc7eb0 to fix RTX issue #1220
Closed saramsey closed 2 years ago
saramsey
commented
3 years ago This appears to have happened in commit 84c8d524b9d6cdd12bb6bd823abf30f8d8dc7eb0 to fix RTX issue #1220
saramsey
commented
3 years ago This appears to be a bug due to commit 84c8d52
saramsey
commented
3 years ago I think this should be a simple fix.
saramsey
commented
3 years ago After my fix, only 284 genes are now being modified:
(base) sramsey-laptop:issue-164 sramsey$ grep 'Genetic locus associated with' kg-ncbi.json | grep full_name | wc -l
284The 284 genes look to be mostly genetic conditions:
(base) sramsey-laptop:issue-164 sramsey$ grep 'Genetic locus associated with' kg-ncbi.json
"full_name": "Genetic locus associated with acrocallosal syndrome",
"name": "Genetic locus associated with ACLS",
"full_name": "Genetic locus associated with albinism-deafness syndrome",
"name": "Genetic locus associated with ADFN",
"full_name": "Genetic locus associated with AF8 temperature sensitivity complementing",
"name": "Genetic locus associated with AF8T",
"full_name": "Genetic locus associated with ankyloblepharon filiforme adnatum",
"name": "Genetic locus associated with AFA",
"full_name": "Genetic locus associated with acrofacial dysostosis 1, Nager type",
"name": "Genetic locus associated with AFD1",
"full_name": "Genetic locus associated with agammaglobulinemia, X-linked 2 (with growth hormone deficiency)",
"name": "Genetic locus associated with AGMX2",
"full_name": "Genetic locus associated with Aicardi syndrome",
"name": "Genetic locus associated with AIC",
"full_name": "Genetic locus associated with amelogenesis imperfecta 3, hypomaturation or hypoplastic type",
"name": "Genetic locus associated with AIH3",
"full_name": "Genetic locus associated with amyotrophic lateral sclerosis 3 (autosomal dominant)",
"name": "Genetic locus associated with ALS3",
"full_name": "Genetic locus associated with arthrogryposis multiplex congenita, neurogenic",
"name": "Genetic locus associated with AMCN",
"full_name": "Genetic locus associated with anophthalmos 1 (with mental retardation, without limb anomalies or dental or urogenital abnormalities)",
"name": "Genetic locus associated with ANOP1",
"full_name": "Genetic locus associated with arrhythmogenic right ventricular dysplasia 3",
"name": "Genetic locus associated with ARVD3",
"full_name": "Genetic locus associated with arrhythmogenic right ventricular dysplasia 4",
"name": "Genetic locus associated with ARVD4",
"full_name": "Genetic locus associated with atrial septal defect 1",
"name": "Genetic locus associated with ASD1",
"full_name": "Genetic locus associated with asphixiating thoracic dystrophy (chondroectodermal dysplasia-like syndrome)",
"name": "Genetic locus associated with ATD",
"full_name": "Genetic locus associated with atherosclerosis susceptibility (lipoprotein associated)",
"name": "Genetic locus associated with ATHS",
"full_name": "Genetic locus associated with azoospermia factor 1",
"name": "Genetic locus associated with AZF1",
"full_name": "Genetic locus associated with B cell CLL/lymphoma 5",
"name": "Genetic locus associated with BCL5",
"full_name": "Genetic locus associated with baboon M7 virus integration site",
"name": "Genetic locus associated with BEVI",
"full_name": "Genetic locus associated with central areolar choroidal dystrophy",
"name": "Genetic locus associated with CACD",
"full_name": "Genetic locus associated with cataract, congenital, cerulean type, 1",
"name": "Genetic locus associated with CCA1",
"full_name": "Genetic locus associated with chondrocalcinosis 1 (calcium pyrophosphate-deposition disease, early onset osteoarthritis)",
"name": "Genetic locus associated with CCAL1",
"full_name": "Genetic locus associated with cataract, congenital, total",
"name": "Genetic locus associated with CCT",
"full_name": "Genetic locus associated with congenital dyserythropoietic anemia, type III",
"name": "Genetic locus associated with CDAN3",
"full_name": "Genetic locus associated with corneal dystrophy of Bowman layer type II (Thiel-Behnke)",
"name": "Genetic locus associated with CDB2",
"full_name": "Genetic locus associated with cognitive function 1, social",
"name": "Genetic locus associated with CGF1",
"full_name": "Genetic locus associated with creatine kinase, ectopic expression",
"name": "Genetic locus associated with CKBE",
"full_name": "Genetic locus associated with cerebellar ataxia 3 (cerebellar parenchyma disorder 1)",
"name": "Genetic locus associated with CLA3",
"full_name": "Genetic locus associated with cardiomyopathy, dilated 1B (autosomal dominant)",
"name": "Genetic locus associated with CMD1B",
"full_name": "Genetic locus associated with cutaneous malignant melanoma/dysplastic nevus",
"name": "Genetic locus associated with CMM",
"full_name": "Genetic locus associated with Charcot-Marie-Tooth neuropathy, X-linked 2 (recessive)",
"name": "Genetic locus associated with CMTX2",
"full_name": "Genetic locus associated with Charcot-Marie-Tooth neuropathy, X-linked 3 (dominant)",
"name": "Genetic locus associated with CMTX3",
"full_name": "Genetic locus associated with cornea plana 1 (autosomal dominant)",
"name": "Genetic locus associated with CNA1",
"full_name": "Genetic locus associated with Carney complex type 2, multiple neoplasia and lentiginosis",
"name": "Genetic locus associated with CNC2",
"full_name": "Genetic locus associated with cone dystrophy 2 (X-linked)",
"name": "Genetic locus associated with COD2",
"full_name": "Genetic locus associated with Coats disease",
"name": "Genetic locus associated with CTD",
"full_name": "Genetic locus associated with cone rod dystrophy 1 (autosomal dominant)",
"name": "Genetic locus associated with CORD1",
"full_name": "Genetic locus associated with cataract, anterior polar 1",
"name": "Genetic locus associated with CTAA1",
"full_name": "Genetic locus associated with cataract, anterior polar 2",
"name": "Genetic locus associated with CTAA2",
"full_name": "Genetic locus associated with coxsackie virus B3 sensitivity",
"name": "Genetic locus associated with CXB3S",
"full_name": "Genetic locus associated with cystoid macular dystrophy",
"name": "Genetic locus associated with CYMD",
"full_name": "Genetic locus associated with deafness, X-linked 3",
"name": "Genetic locus associated with DFNX3",
"full_name": "Genetic locus associated with deafness, autosomal dominant 7",
"name": "Genetic locus associated with DFNA7",
"full_name": "Genetic locus associated with deafness, autosomal dominant 16",
"name": "Genetic locus associated with DFNA16",
"full_name": "Genetic locus associated with deafness, autosomal recessive 5",
"name": "Genetic locus associated with DFNB5",
"full_name": "Genetic locus associated with deafness, autosomal recessive 13",
"name": "Genetic locus associated with DFNB13",
"full_name": "Genetic locus associated with deafness, autosomal recessive 14",
"name": "Genetic locus associated with DFNB14",
"full_name": "Genetic locus associated with deafness, autosomal recessive 17",
"name": "Genetic locus associated with DFNB17",
"full_name": "Genetic locus associated with deafness, autosomal recessive 20",
"name": "Genetic locus associated with DFNB20",
"full_name": "Genetic locus associated with diaphragmatic hernia 1",
"name": "Genetic locus associated with DIH1",
"full_name": "Genetic locus associated with dandy-walker syndrome",
"name": "Genetic locus associated with DWS",
"full_name": "Genetic locus associated with dystonia 7, torsion (autosomal dominant)",
"name": "Genetic locus associated with DYT7",
"full_name": "Genetic locus associated with dyslexia susceptibility 1",
"name": "Genetic locus associated with DYX1",
"full_name": "Genetic locus associated with ECHO virus (serotypes 4, 6, 11, 19) sensitivity",
"name": "Genetic locus associated with E11S",
"full_name": "Genetic locus associated with epidermolysis bullosa, macular type",
"name": "Genetic locus associated with EBM",
"full_name": "Genetic locus associated with epidermolysis bullosa 3, progressiva",
"name": "Genetic locus associated with EBR3",
"full_name": "Genetic locus associated with ectrodactyly, ectodermal dysplasia and cleft lip/palate syndrome 1",
"name": "Genetic locus associated with EEC1",
"full_name": "Genetic locus associated with electro-encephalographic variant pattern 1",
"name": "Genetic locus associated with EEGV1",
"full_name": "Genetic locus associated with epilepsy, generalized, idiopathic",
"name": "Genetic locus associated with EGI",
"full_name": "Genetic locus associated with enuresis, nocturnal 1",
"name": "Genetic locus associated with ENUR1",
"full_name": "Genetic locus associated with enuresis, nocturnal 2",
"name": "Genetic locus associated with ENUR2",
"full_name": "Genetic locus associated with excision repair complementing defective repair in mouse cells",
"name": "Genetic locus associated with ERCM1",
"full_name": "Genetic locus associated with essential tremor 2",
"name": "Genetic locus associated with ETM2",
"full_name": "Genetic locus associated with exostoses (multiple) 3",
"name": "Genetic locus associated with EXT3",
"full_name": "Genetic locus associated with F-cell production 1",
"name": "Genetic locus associated with FCP1",
"full_name": "Genetic locus associated with febrile convulsions 1",
"name": "Genetic locus associated with FEB1",
"full_name": "Genetic locus associated with febrile convulsions 2",
"name": "Genetic locus associated with FEB2",
"full_name": "Genetic locus associated with FG syndrome 2",
"name": "Genetic locus associated with FGS2",
"full_name": "Genetic locus associated with Friedreich ataxia 2",
"name": "Genetic locus associated with FRDA2",
"full_name": "Genetic locus associated with facioscapulohumeral muscular dystrophy 1A",
"name": "Genetic locus associated with FSHMD1A",
"full_name": "Genetic locus associated with facioscapulohumeral muscular dystrophy 1B",
"name": "Genetic locus associated with FSHMD1B",
"full_name": "Genetic locus associated with polykaryocytosis promoter",
"name": "Genetic locus associated with FUSE",
"full_name": "Genetic locus associated with growth control, Y chromosome influenced",
"name": "Genetic locus associated with GCY",
"full_name": "Genetic locus associated with glaucoma 1, open angle, B (adult-onset)",
"name": "Genetic locus associated with GLC1B",
"full_name": "Genetic locus associated with glaucoma 1, open angle, C",
"name": "Genetic locus associated with GLC1C",
"full_name": "Genetic locus associated with glaucoma 1, open angle, D (adult-onset)",
"name": "Genetic locus associated with GLC1D",
"full_name": "Genetic locus associated with glaucoma 3, primary infantile, B",
"name": "Genetic locus associated with GLC3B",
"full_name": "Genetic locus associated with glycosuria 1, renal",
"name": "Genetic locus associated with GLYS1",
"full_name": "Genetic locus associated with geniospasm 1",
"name": "Genetic locus associated with GSM1",
"full_name": "Genetic locus associated with Gilles de la Tourette syndrome",
"name": "Genetic locus associated with GTS",
"full_name": "Genetic locus associated with hair color 2 (red)",
"name": "Genetic locus associated with HCL2",
"full_name": "Genetic locus associated with human coronavirus sensitivity",
"name": "Genetic locus associated with HCVS",
"full_name": "Genetic locus associated with holoprosencephaly 1, alobar",
"name": "Genetic locus associated with HPE1",
"full_name": "Genetic locus associated with hereditary persistence of fetal hemoglobin, heterocellular, Indian type",
"name": "Genetic locus associated with HPFH2",
"full_name": "Genetic locus associated with hypoparathyroidism",
"name": "Genetic locus associated with HPT",
"full_name": "Genetic locus associated with hypertrichosis 1 (universalis, congenital)",
"name": "Genetic locus associated with HTC1",
"full_name": "Genetic locus associated with hypertrichosis 2 (generalized, congenital)",
"name": "Genetic locus associated with HTC2",
"full_name": "Genetic locus associated with high L-leucine transport",
"name": "Genetic locus associated with HTL",
"full_name": "Genetic locus associated with inflammatory bowel disease 2",
"name": "Genetic locus associated with IBD2",
"full_name": "Genetic locus associated with insulin dependent diabetes mellitus 3",
"name": "Genetic locus associated with IDDM3",
"full_name": "Genetic locus associated with insulin dependent diabetes mellitus 4",
"name": "Genetic locus associated with IDDM4",
"full_name": "Genetic locus associated with insulin dependent diabetes mellitus 6",
"name": "Genetic locus associated with IDDM6",
"full_name": "Genetic locus associated with insulin dependent diabetes mellitus 7",
"name": "Genetic locus associated with IDDM7",
"full_name": "Genetic locus associated with insulin dependent diabetes mellitus 8",
"name": "Genetic locus associated with IDDM8",
"full_name": "Genetic locus associated with insulin dependent diabetes mellitus 11",
"name": "Genetic locus associated with IDDM11",
"full_name": "Genetic locus associated with insulin dependent diabetes mellitus 13",
"name": "Genetic locus associated with IDDM13",
"full_name": "Genetic locus associated with insulin dependent diabetes mellitus 15",
"name": "Genetic locus associated with IDDM15",
"full_name": "Genetic locus associated with immunoglobulin E concentration, serum",
"name": "Genetic locus associated with IGES",
"full_name": "Genetic locus associated with iris hypoplasia with glaucoma 1",
"name": "Genetic locus associated with IHG1",
"full_name": "Genetic locus associated with Jacobsen syndrome",
"name": "Genetic locus associated with JBS",
"full_name": "Genetic locus associated with keratolytic winter erythema (Oudtshoorn skin disease)",
"name": "Genetic locus associated with KWE",
"full_name": "Genetic locus associated with lymphokine-activated killer cell ligand",
"name": "Genetic locus associated with LAKLG",
"full_name": "Genetic locus associated with microphthalmia or anophthalmia and associated anomalies",
"name": "Genetic locus associated with MAA",
"full_name": "Genetic locus associated with major affective disorder 1",
"name": "Genetic locus associated with MAFD1",
"full_name": "Genetic locus associated with major affective disorder 2",
"name": "Genetic locus associated with MAFD2",
"full_name": "Genetic locus associated with Moebius syndrome 1",
"name": "Genetic locus associated with MBS1",
"full_name": "Genetic locus associated with macular dystrophy, retinal, 1 (North Carolina type)",
"name": "Genetic locus associated with MCDR1",
"full_name": "Genetic locus associated with muscular dystrophy, with rimmed vacuoles",
"name": "Genetic locus associated with MDRV",
"full_name": "Genetic locus associated with malignant hyperthermia susceptibility 2",
"name": "Genetic locus associated with MHS2",
"full_name": "Genetic locus associated with malignant hyperthermia susceptibility 4",
"name": "Genetic locus associated with MHS4",
"full_name": "Genetic locus associated with malignant hyperthermia susceptibility 6",
"name": "Genetic locus associated with MHS6",
"full_name": "Genetic locus associated with mental retardation-skeletal dysplasia",
"name": "Genetic locus associated with MRSD",
"full_name": "Genetic locus associated with mental retardation, X-linked 14",
"name": "Genetic locus associated with MRX14",
"full_name": "Genetic locus associated with mental retardation, X-linked 20",
"name": "Genetic locus associated with MRX20",
"full_name": "Genetic locus associated with mental retardation, X-linked 23",
"name": "Genetic locus associated with MRX23",
"full_name": "Genetic locus associated with multiple sclerosis",
"name": "Genetic locus associated with MS",
"full_name": "Genetic locus associated with mental retardation, X-linked 42",
"name": "Genetic locus associated with MRX42",
"full_name": "Genetic locus associated with mental retardation, X-linked 49",
"name": "Genetic locus associated with MRX49",
"full_name": "Genetic locus associated with mental retardation, X-linked 53",
"name": "Genetic locus associated with MRX53",
"full_name": "Genetic locus associated with mental retardation, X-linked, syndromic 7",
"name": "Genetic locus associated with MRXS7",
"full_name": "Genetic locus associated with microcephaly with spastic diplegia (Paine syndrome)",
"name": "Genetic locus associated with MSD",
"full_name": "Genetic locus associated with myopia 1 (X-linked)",
"name": "Genetic locus associated with MYP1",
"full_name": "Genetic locus associated with myopia 2 (high grade, autosomal dominant)",
"name": "Genetic locus associated with MYP2",
"full_name": "Genetic locus associated with non insulin dependent diabetes mellitus 1",
"name": "Genetic locus associated with NIDDM1",
"full_name": "Genetic locus associated with non insulin dependent diabetes mellitus 2",
"name": "Genetic locus associated with NIDDM2",
"full_name": "Genetic locus associated with natural killer cell susceptibility 1",
"name": "Genetic locus associated with NKS1",
"full_name": "Genetic locus associated with neutrophil migration",
"name": "Genetic locus associated with NM",
"full_name": "Genetic locus associated with nystagmus 2, congenital autosomal dominant",
"name": "Genetic locus associated with NYS2",
"full_name": "Genetic locus associated with nystagmus 3, congenital autosomal dominant",
"name": "Genetic locus associated with NYS3",
"full_name": "Genetic locus associated with ocular albinism and sensorineural deafness",
"name": "Genetic locus associated with OASD",
"full_name": "Genetic locus associated with orofacial cleft 1",
"name": "Genetic locus associated with OFC1",
"full_name": "Genetic locus associated with orofacial cleft 2",
"name": "Genetic locus associated with OFC2",
"full_name": "Genetic locus associated with orofacial cleft 3",
"name": "Genetic locus associated with OFC3",
"full_name": "Genetic locus associated with optic atrophy 2 (obscure)",
"name": "Genetic locus associated with OPA2",
"full_name": "Genetic locus associated with ophthalmoplegia, external, with myopia",
"name": "Genetic locus associated with OPEM",
"full_name": "Genetic locus associated with otosclerosis 1",
"name": "Genetic locus associated with OTSC1",
"full_name": "Genetic locus associated with Parkinson disease 3 (autosomal dominant, Lewy body)",
"name": "Genetic locus associated with PARK3",
"full_name": "Genetic locus associated with polycystic ovary syndrome 1",
"name": "Genetic locus associated with PCOS1",
"full_name": "Genetic locus associated with Paget disease of bone 1",
"name": "Genetic locus associated with PDB1",
"full_name": "Genetic locus associated with pigment disorder, reticulate",
"name": "Genetic locus associated with PDR",
"full_name": "Genetic locus associated with preeclampsia/eclampsia 1",
"name": "Genetic locus associated with PEE1",
"full_name": "Genetic locus associated with polycystic kidney disease 3 (autosomal dominant)",
"name": "Genetic locus associated with PKD3",
"full_name": "Genetic locus associated with primary retinal dysplasia",
"name": "Genetic locus associated with PRD",
"full_name": "Genetic locus associated with Prieto X-linked mental retardation syndrome",
"name": "Genetic locus associated with PRS",
"full_name": "Genetic locus associated with ptosis, congenital 1 (autosomal dominant)",
"name": "Genetic locus associated with PTOS1",
"full_name": "Genetic locus associated with retinal cone dystrophy 1",
"name": "Genetic locus associated with RCD1",
"full_name": "Genetic locus associated with Rieger syndrome 2",
"name": "Genetic locus associated with RIEG2",
"full_name": "Genetic locus associated with rippling muscle disease 1",
"name": "Genetic locus associated with RMD1",
"full_name": "Genetic locus associated with retinitis pigmentosa 6 (X-linked recessive)",
"name": "Genetic locus associated with RP6",
"full_name": "Genetic locus associated with retinitis pigmentosa 22 (autosomal recessive)",
"name": "Genetic locus associated with RP22",
"full_name": "Genetic locus associated with retinitis pigmentosa 24 (X-linked recessive)",
"name": "Genetic locus associated with RP24",
"full_name": "Genetic locus associated with suppression of anchorage independence 1",
"name": "Genetic locus associated with SAI1",
"full_name": "Genetic locus associated with schizophrenia disorder 3",
"name": "Genetic locus associated with SCZD3",
"full_name": "Genetic locus associated with schizophrenia disorder 1",
"name": "Genetic locus associated with SCZD1",
"full_name": "Genetic locus associated with schizophrenia disorder 2",
"name": "Genetic locus associated with SCZD2",
"full_name": "Genetic locus associated with Stoltzfus blood group",
"name": "Genetic locus associated with SF",
"full_name": "Genetic locus associated with split hand/foot malformation (ectrodactyly) type 2",
"name": "Genetic locus associated with SHFM2",
"full_name": "Genetic locus associated with spastic paraplegia 5B (autosomal recessive)",
"name": "Genetic locus associated with SPG5B",
"full_name": "Genetic locus associated with suppression of tumorigenicity 2",
"name": "Genetic locus associated with ST2",
"full_name": "Genetic locus associated with suppression of tumorigenicity 3",
"name": "Genetic locus associated with ST3",
"full_name": "Genetic locus associated with suppression of tumorigenicity 8 (ovarian)",
"name": "Genetic locus associated with ST8",
"full_name": "Genetic locus associated with total anomalous pulmonary venous return 1",
"name": "Genetic locus associated with TAPVR1",
"full_name": "Genetic locus associated with thoracoabdominal syndrome",
"name": "Genetic locus associated with THAS",
"full_name": "Genetic locus associated with thymoma",
"name": "Genetic locus associated with THM",
"full_name": "Genetic locus associated with torticollis, keloids, cryptorchidism and renal dysplasia",
"name": "Genetic locus associated with TKCR",
"full_name": "Genetic locus associated with sclerotylosis",
"name": "Genetic locus associated with TYS",
"full_name": "Genetic locus associated with Usher syndrome 1E (autosomal recessive, severe)",
"name": "Genetic locus associated with USH1E",
"full_name": "Genetic locus associated with vesicular stomatitis virus defective interfering particle suppression",
"name": "Genetic locus associated with VDI",
"full_name": "Genetic locus associated with vitelliform macular dystrophy, atypical",
"name": "Genetic locus associated with VMD1",
"full_name": "Genetic locus associated with atrioventricular septal defect 1",
"name": "Genetic locus associated with AVSD1",
"full_name": "Genetic locus associated with Waardenburg syndrome, type 2B",
"name": "Genetic locus associated with WS2B",
"full_name": "Genetic locus associated with Wilms tumor 2",
"name": "Genetic locus associated with WT2",
"full_name": "Genetic locus associated with Xm(a) antigen",
"name": "Genetic locus associated with XM",
"full_name": "Genetic locus associated with X-linked suppressor of LU antigens",
"name": "Genetic locus associated with XS",
"full_name": "Genetic locus associated with cataract, congenital, Volkmann type",
"name": "Genetic locus associated with CCV",
"full_name": "Genetic locus associated with Methylation modifier for class I HLA",
"name": "Genetic locus associated with MEMO1",
"full_name": "Genetic locus associated with Acute insulin response (2)",
"name": "Genetic locus associated with AIR",
"full_name": "Genetic locus associated with Minisatellite 33.6",
"name": "Genetic locus associated with D1S111",
"full_name": "Genetic locus associated with Pseudohypoaldosteronism type II (gene A)",
"name": "Genetic locus associated with PHA2A",
"full_name": "Genetic locus associated with predisposing for prostate cancer",
"name": "Genetic locus associated with PCAP",
"full_name": "Genetic locus associated with Leptin, serum levels of",
"name": "Genetic locus associated with LEPQTL1",
"full_name": "Genetic locus associated with small cell cancer of the lung",
"name": "Genetic locus associated with SCLC1",
"full_name": "Genetic locus associated with Moebius syndrome 2",
"name": "Genetic locus associated with MBS2",
"full_name": "Genetic locus associated with Craniosynostosis, Adelaide type",
"name": "Genetic locus associated with CRSA",
"full_name": "Genetic locus associated with psoriasis susceptibility 3",
"name": "Genetic locus associated with PSORS3",
"full_name": "Genetic locus associated with Fecundity gene, Boorla, of sheep, homolog of",
"name": "Genetic locus associated with FECB",
"full_name": "Genetic locus associated with Leukocyte antigen group 5",
"name": "Genetic locus associated with LAG5",
"full_name": "Genetic locus associated with Temperature sensitivity complementation, ts13",
"name": "Genetic locus associated with TS13",
"full_name": "Genetic locus associated with eosinophilia, familial",
"name": "Genetic locus associated with EOS",
"full_name": "Genetic locus associated with hemangioma, capillary, hereditary",
"name": "Genetic locus associated with HEMC",
"full_name": "Genetic locus associated with Plasmodium falciparum blood infection levels",
"name": "Genetic locus associated with PFBI",
"full_name": "Genetic locus associated with Schistosoma mansoni, susceptibility/resistance to",
"name": "Genetic locus associated with SM1",
"full_name": "Genetic locus associated with immune response to synthetic polypeptides 1",
"name": "Genetic locus associated with IGLP1",
"full_name": "Genetic locus associated with immune response to synthetic polypeptides 2",
"name": "Genetic locus associated with IGLP2",
"full_name": "Genetic locus associated with Immune response to synthetic polypeptide--IRGAT",
"name": "Genetic locus associated with IGAT",
"full_name": "Genetic locus associated with Immune suppression to streptococcal antigen",
"name": "Genetic locus associated with ISCW",
"full_name": "Genetic locus associated with ossification of posterior longitudinal ligament of spine",
"name": "Genetic locus associated with OPLL",
"full_name": "Genetic locus associated with Ragweed sensitivity",
"name": "Genetic locus associated with RWS",
"full_name": "Genetic locus associated with Laryngeal adductor paralysis",
"name": "Genetic locus associated with LAP",
"full_name": "Genetic locus associated with pelviureteric junction obstruction",
"name": "Genetic locus associated with PUJO",
"full_name": "Genetic locus associated with progressive bifocal chorioretinal atrophy 1",
"name": "Genetic locus associated with PBCRA1",
"full_name": "Genetic locus associated with hereditary persistence of fetal hemoglobin, heterocellular",
"name": "Genetic locus associated with HBFQTL2",
"full_name": "Genetic locus associated with Pancreatic beta cell, agenesis of",
"name": "Genetic locus associated with PBCA",
"full_name": "Genetic locus associated with Temperature sensitivity complementation, cell cycle specific",
"name": "Genetic locus associated with TS546",
"full_name": "Genetic locus associated with Goldenhar syndrome",
"name": "Genetic locus associated with GHS",
"full_name": "Genetic locus associated with Hyperreflexia",
"name": "Genetic locus associated with HRX",
"full_name": "Genetic locus associated with Malignant hyperthermia susceptibility 3",
"name": "Genetic locus associated with MHS3",
"full_name": "Genetic locus associated with glaucoma-related pigment dispersion syndrome 1",
"name": "Genetic locus associated with GPDS1",
"full_name": "Genetic locus associated with Lymphomatous acute lymphoblastic leukemia",
"name": "Genetic locus associated with LALL",
"full_name": "Genetic locus associated with Melkersson-Rosenthal syndrome",
"name": "Genetic locus associated with MROS",
"full_name": "Genetic locus associated with Temperature sensitivity complementation, H142",
"name": "Genetic locus associated with H142T",
"full_name": "Genetic locus associated with refsum disease, adult, with increased pipecolicacidemia",
"name": "Genetic locus associated with RDPA",
"full_name": "Genetic locus associated with DiGeorge syndrome/velocardiofacial syndrome complex 2",
"name": "Genetic locus associated with DGS2",
"full_name": "Genetic locus associated with Proline(-) auxotroph, complementation of",
"name": "Genetic locus associated with PROA",
"full_name": "Genetic locus associated with erythrocytosis, autosomal recessive benign 2",
"name": "Genetic locus associated with ECB2",
"full_name": "Genetic locus associated with Anal canal carcinoma",
"name": "Genetic locus associated with ANC",
"full_name": "Genetic locus associated with Breast cancer, 11;22 translocation associated",
"name": "Genetic locus associated with BRCATA",
"full_name": "Genetic locus associated with hypertension with brachydactyly",
"name": "Genetic locus associated with HTNB",
"full_name": "Genetic locus associated with Alzheimer disease 5",
"name": "Genetic locus associated with AD5",
"full_name": "Genetic locus associated with scapuloperoneal syndrome, myopathic type",
"name": "Genetic locus associated with SPPM",
"full_name": "Genetic locus associated with male germ cell tumor",
"name": "Genetic locus associated with MGCT",
"full_name": "Genetic locus associated with spinal muscular atrophy, congenital nonprogressive, of lower limbs",
"name": "Genetic locus associated with SMAL",
"full_name": "Genetic locus associated with Disrupted in B-cell neoplasia",
"name": "Genetic locus associated with CLLS2",
"full_name": "Genetic locus associated with X-ray sensitivity",
"name": "Genetic locus associated with XRS",
"full_name": "Genetic locus associated with postaxial polydactyly, type A2",
"name": "Genetic locus associated with PAPA2",
"full_name": "Genetic locus associated with microcoria, congenital",
"name": "Genetic locus associated with MCOR",
"full_name": "Genetic locus associated with cancer, familial, with in vitro radioresistance",
"name": "Genetic locus associated with BRCD1",
"full_name": "Genetic locus associated with microphthalmia, autosomal recessive",
"name": "Genetic locus associated with MCOP1",
"full_name": "Genetic locus associated with inversus situs, viscerum",
"name": "Genetic locus associated with IV",
"full_name": "Genetic locus associated with Mental retardation, severe, with spasticity and tapetoretinal",
"name": "Genetic locus associated with MRST",
"full_name": "Genetic locus associated with alpha-thalassemia/mental retardation syndrome, type 1",
"name": "Genetic locus associated with HBHR",
"full_name": "Genetic locus associated with cataract, congenital, with microphthalmia",
"name": "Genetic locus associated with MCOPCT1",
"full_name": "Genetic locus associated with polycystic kidney disease, infantile severe, with tuberous sclerosis",
"name": "Genetic locus associated with PKDTS",
"full_name": "Genetic locus associated with Wilms tumor-3",
"name": "Genetic locus associated with WT3",
"full_name": "Genetic locus associated with hypodontia 2 (autosomal recessive)",
"name": "Genetic locus associated with HYD2",
"full_name": "Genetic locus associated with myasthenia gravis, familial infantile, 1",
"name": "Genetic locus associated with CMS1A1",
"full_name": "Genetic locus associated with Wilms tumor-4",
"name": "Genetic locus associated with WT4",
"full_name": "Genetic locus associated with gliosis, familial progressive subcortical",
"name": "Genetic locus associated with GPSC",
"full_name": "Genetic locus associated with Carnosinemia (carnosinase)",
"name": "Genetic locus associated with CNSN",
"full_name": "Genetic locus associated with Oncogene liposarcoma (DNA segment, single copy, expressed, probes",
"name": "Genetic locus associated with LPSA",
"full_name": "Genetic locus associated with benign familial infantile convulsions",
"name": "Genetic locus associated with BFIS1",
"full_name": "Genetic locus associated with Progressive familial heart block, type I, locus 1",
"name": "Genetic locus associated with HBN1",
"full_name": "Genetic locus associated with Nerve growth factor, gamma subunit",
"name": "Genetic locus associated with NGFG",
"full_name": "Genetic locus associated with Myeloid leukemia-related gene (myeloid tumor suppressor)",
"name": "Genetic locus associated with MLRL",
"full_name": "Genetic locus associated with Myeloproliferative syndrome, transient (transient abnormal",
"name": "Genetic locus associated with TAM",
"full_name": "Genetic locus associated with Beta-amino acids, renal transport of",
"name": "Genetic locus associated with AABT",
"full_name": "Genetic locus associated with Beta-adrenergic stimulation, response to",
"name": "Genetic locus associated with BAS",
"full_name": "Genetic locus associated with Opitz G syndrome, type II",
"name": "Genetic locus associated with OGS2",
"full_name": "Genetic locus associated with Corneal dermoids",
"name": "Genetic locus associated with CND",
"full_name": "Genetic locus associated with Diabetes mellitus, insulin-dependent, X-linked, susceptibility to",
"name": "Genetic locus associated with IDDMX",
"full_name": "Genetic locus associated with Mental retardation, X-linked, syndromic 12",
"name": "Genetic locus associated with MRXS12",
"full_name": "Genetic locus associated with Migraine, familial typical, susceptibility to",
"name": "Genetic locus associated with MGR2",
"full_name": "Genetic locus associated with Bazex syndrome",
"name": "Genetic locus associated with BZX",
"full_name": "Genetic locus associated with Gustavson mental retardation syndrome (with microcephaly, optic",
"name": "Genetic locus associated with GUST",
"full_name": "Genetic locus associated with Immunoneurologic syndrome X-linked, of Wood, Black, and Norbury",
"name": "Genetic locus associated with INDX",
"full_name": "Genetic locus associated with Intestinal pseudoobstruction, neuronal, primary idiopathic",
"name": "Genetic locus associated with IPOX",
"full_name": "Genetic locus associated with schizophrenia disorder 6",
"name": "Genetic locus associated with SCZD6",
"full_name": "Genetic locus associated with schizophrenia disorder 7",
"name": "Genetic locus associated with SCZD7",
"full_name": "Genetic locus associated with mental retardation, epileptic seizures, hypogonadism and -genitalism, microcephaly and obesity syndrome",
"name": "Genetic locus associated with MEHMO",
"full_name": "Genetic locus associated with suppression of tumorigenicity 11 (pancreas)",
"name": "Genetic locus associated with ST11",
"full_name": "Genetic locus associated with insulin dependent diabetes mellitus 17",
"name": "Genetic locus associated with IDDM17",
"full_name": "Genetic locus associated with myopia 3 (high grade, autosomal dominant)",
"name": "Genetic locus associated with MYP3",
"full_name": "Genetic locus associated with schizophrenia disorder 8",
"name": "Genetic locus associated with SCZD8",
"full_name": "Genetic locus associated with patella aplasia-hypoplasia",
"name": "Genetic locus associated with PTLAH",
"full_name": "Genetic locus associated with hereditary prostate cancer, X-linked",
"name": "Genetic locus associated with HPCX",
"full_name": "Genetic locus associated with episodic muscle weakness, X-linked",
"name": "Genetic locus associated with EMWX",
"full_name": "Genetic locus associated with cystic fibrosis modifier 1",
"name": "Genetic locus associated with CFM1",
"full_name": "Genetic locus associated with Mesomelic dysplasia, Kantaputra type",
"name": "Genetic locus associated with MMDK",
"full_name": "Genetic locus associated with Cataract, posterior polar",
"name": "Genetic locus associated with CTPP",
"full_name": "Genetic locus associated with Mental health wellness 1",
"name": "Genetic locus associated with MHW1",
"full_name": "Genetic locus associated with psoriasis susceptibility 4",
"name": "Genetic locus associated with PSORS4",
"full_name": "Genetic locus associated with Duane retraction syndrome 1",
"name": "Genetic locus associated with DURS1",
"full_name": "Genetic locus associated with dehydrated hereditary stomatocytosis",
"name": "Genetic locus associated with DHS",
"full_name": "Genetic locus associated with immunoglobulin A (IgA) deficiency susceptibility 1",
"name": "Genetic locus associated with IGAD1",
"full_name": "Genetic locus associated with dyslexia susceptibility 3",
"name": "Genetic locus associated with DYX3",
"full_name": "Genetic locus associated with Moebius syndrome 3",
"name": "Genetic locus associated with MBS3",
"full_name": "Genetic locus associated with cardiomyopathy, dilated 1H (autosomal dominant)",
"name": "Genetic locus associated with CMD1H",
"full_name": "Genetic locus associated with nanophthalmos 1",
"name": "Genetic locus associated with NNO1",
"full_name": "Genetic locus associated with mental retardation, X-linked 73",
"name": "Genetic locus associated with MRX73",
"full_name": "Genetic locus associated with idiopathic basal ganglia calcification 1",
"name": "Genetic locus associated with IBGC1",
"full_name": "Genetic locus associated with deafness, autosomal recessive 27",
"name": "Genetic locus associated with DFNB27",
"full_name": "Genetic locus associated with deafness, autosomal dominant 30",
"name": "Genetic locus associated with DFNA30",
"full_name": "Genetic locus associated with deafness, autosomal dominant 24",
"name": "Genetic locus associated with DFNA24",
"full_name": "Genetic locus associated with diabetic nephropathy",
"name": "Genetic locus associated with DIANPH",Commit 81254ac should fix the issue.
saramsey
commented
3 years ago Tagging @edeutsch and @acevedol so they are aware that the fix is implemented in code in the RTX-KG2 master branch, and thus ready to be included in the KG2.7.4 build.
edeutsch
commented
3 years ago This looks very good, thanks!
This issue was first reported by @edeutsch in RTX issue 1699.