Move human function description in elegans gene descriptions after the orthology sentence in order to improve readability and avoid confusion.
Current description:
WB:WBGene00000065 act-3
Expressed in gonad and head. Human ortholog(s) of this gene implicated in several diseases, including Baraitser-Winter syndrome 1; Baraitser-Winter syndrome 2; and autosomal dominant nonsyndromic deafness 20. Human ACTB Contributes to nucleosomal DNA binding activity. Human ACTB enables several functions, including Tat protein binding activity; enzyme binding activity; and kinesin binding activity. A structural constituent of postsynaptic actin cytoskeleton. Is predicted to encode a protein with the following domains: Actin family; Phosphorylation site; ATPase, nucleotide binding domain; and Actin. Is an ortholog of human ACTB (actin beta).
What it should be:
Expressed in gonad and head. Human ortholog(s) of this gene implicated in several diseases, including Baraitser-Winter syndrome 1; Baraitser-Winter syndrome 2; and autosomal dominant nonsyndromic deafness 20. A structural constituent of postsynaptic actin cytoskeleton. Is predicted to encode a protein with the following domains: Actin family; Phosphorylation site; ATPase, nucleotide binding domain; and Actin. Is an ortholog of human ACTB (actin beta). Human ACTB Contributes to nucleosomal DNA binding activity. Human ACTB enables several functions, including Tat protein binding activity; enzyme binding activity; and kinesin binding activity.
I can see that the human function sentence (either "enables" or "contributes") has been moved to the end of the description, so this issue has been resolved.
Move human function description in elegans gene descriptions after the orthology sentence in order to improve readability and avoid confusion.
Current description:
WB:WBGene00000065 act-3 Expressed in gonad and head. Human ortholog(s) of this gene implicated in several diseases, including Baraitser-Winter syndrome 1; Baraitser-Winter syndrome 2; and autosomal dominant nonsyndromic deafness 20. Human ACTB Contributes to nucleosomal DNA binding activity. Human ACTB enables several functions, including Tat protein binding activity; enzyme binding activity; and kinesin binding activity. A structural constituent of postsynaptic actin cytoskeleton. Is predicted to encode a protein with the following domains: Actin family; Phosphorylation site; ATPase, nucleotide binding domain; and Actin. Is an ortholog of human ACTB (actin beta).
What it should be: Expressed in gonad and head. Human ortholog(s) of this gene implicated in several diseases, including Baraitser-Winter syndrome 1; Baraitser-Winter syndrome 2; and autosomal dominant nonsyndromic deafness 20. A structural constituent of postsynaptic actin cytoskeleton. Is predicted to encode a protein with the following domains: Actin family; Phosphorylation site; ATPase, nucleotide binding domain; and Actin. Is an ortholog of human ACTB (actin beta). Human ACTB Contributes to nucleosomal DNA binding activity. Human ACTB enables several functions, including Tat protein binding activity; enzyme binding activity; and kinesin binding activity.