7 results (0.01 seconds)

gene: rhr-1 [Browse genome (BioProject PRJNA13758)] [Search on AGR]

Caenorhabditis elegans

Enables ammonium channel activity. Involved in ammonium transmembrane transport. Predicted to be located in plasma membrane. Expressed in head. Human ortholog(s) of this gene implicated in Rh deficiency syndrome; Rh isoimmunization; and overhydrated hereditary stomatocytosis. Is an ortholog of human RHAG (Rh associated glycoprotein); RHBG (Rh family B glycoprotein); and RHCG (Rh family C glycoprotein).

gene: rhr-2 [Browse genome (BioProject PRJNA13758)] [Search on AGR]

Caenorhabditis elegans

Predicted to enable ammonium channel activity. Predicted to be involved in ammonium homeostasis and ammonium transmembrane transport. Located in apical plasma membrane. Expressed in several structures, including body wall musculature; head neurons; spermatheca; ventral nerve cord; and vulva. Human ortholog(s) of this gene implicated in Rh deficiency syndrome and overhydrated hereditary stomatocytosis. Is an ortholog of human RHAG (Rh associated glycoprotein); RHBG (Rh family B glycoprotein); and RHCG (Rh family C glycoprotein).

strain: DR1809

Caenorhabditis elegans

gene: Y6B3B.9 [Browse genome (BioProject PRJNA13758)] [Search on AGR]

Caenorhabditis elegans

Predicted to enable endonuclease activity. Predicted to be involved in maturation of 5.8S rRNA and maturation of LSU-rRNA. Predicted to be part of preribosome, large subunit precursor. Human ortholog(s) of this gene implicated in Wilson-Turner syndrome. Is an ortholog of human LAS1L (LAS1 like ribosome biogenesis factor).

strain: KR1504

Caenorhabditis elegans

gene: amt-2 [Browse genome (BioProject PRJNA13758)] [Search on AGR]

Caenorhabditis elegans

Predicted to enable ammonium channel activity. Predicted to be involved in ammonium homeostasis and ammonium transmembrane transport. Predicted to be located in plasma membrane.

gene: eel-1 [Browse genome (BioProject PRJNA13758)] [Search on AGR]

Caenorhabditis elegans

Predicted to enable ubiquitin protein ligase activity. Involved in several processes, including asymmetric protein localization involved in cell fate determination; hemidesmosome assembly; and signal transduction in response to DNA damage. Predicted to be located in cytoplasm and nucleus. Expressed in several structures, including hermaphrodite gonad; intestine; neurons; pharynx; and vulva. Used to study syndromic X-linked intellectual disability. Human ortholog(s) of this gene implicated in syndromic X-linked intellectual disability Turner type. Is an ortholog of human HUWE1 (HECT, UBA and WWE domain containing E3 ubiquitin protein ligase 1).