BX106

Caenorhabditis elegans

CZ29326

Caenorhabditis elegans

TP66

Caenorhabditis elegans

TP67

Caenorhabditis elegans

BX107

Caenorhabditis elegans

KA6

Caenorhabditis elegans

act-4

Caenorhabditis elegans

Predicted to be a structural constituent of cytoskeleton. Predicted to be involved in actin cytoskeleton organization and mitotic cytokinesis. Located in striated muscle thin filament. Expressed in body wall musculature; gonad; spermatheca; and vulval muscle. 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. Is an ortholog of human ACTB (actin beta).

CZ29114

Caenorhabditis elegans

act-3

Caenorhabditis elegans

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. Is an ortholog of human ACTB (actin beta). Human ACTB contributes to nucleosomal DNA binding activity. Human ACTB enables several functions, including ATP hydrolysis activity; Tat protein binding activity; and enzyme binding activity. Human ACTB is a structural constituent of postsynaptic actin cytoskeleton.

act-1

Caenorhabditis elegans

Predicted to be a structural constituent of cytoskeleton. Involved in cortical actin cytoskeleton organization; embryo development; and mitotic cytokinesis. Located in striated muscle thin filament. Expressed in body wall musculature and gonad. 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. Is an ortholog of human ACTB (actin beta).