- Or22c [Search on AGR]
Drosophila melanogaster Odorant receptor 22c (Or22c) encodes a multi-transmembrane chemoreceptor that mediates response to volatile chemicals.
- wdr-60 [Browse genome (BioProject PRJNA13758)] [Search on AGR]
Caenorhabditis elegans Predicted to enable dynein heavy chain binding activity and dynein light chain binding activity. Predicted to be involved in intraciliary transport. Predicted to be located in ciliary plasm. Predicted to be part of cytoplasmic dynein complex. Used to study short-rib thoracic dysplasia 8 with or without polydactyly. Human ortholog(s) of this gene implicated in short-rib thoracic dysplasia 8 with or without polydactyly. Is an ortholog of human DYNC2I1 (dynein 2 intermediate chain 1).
- TACR3-AS1 [Search on AGR]
Homo sapiens ASSOCIATED WITH genetic disease; hypogonadotropic hypogonadism 11 with or without anosmia; hypogonadotropic hypogonadism 12 with or without anosmia
- tkr-2 [Browse genome (BioProject PRJNA13758)] [Search on AGR]
Caenorhabditis elegans Predicted to enable neuropeptide receptor activity. Predicted to be involved in neuropeptide signaling pathway. Predicted to be located in plasma membrane. Human ortholog(s) of this gene implicated in exercise-induced bronchoconstriction and hypogonadotropic hypogonadism 11 with or without anosmia. Is an ortholog of human TACR2 (tachykinin receptor 2).
- ARL14EP-DT [Search on AGR]
Homo sapiens ASSOCIATED WITH genetic disease; hypogonadotropic hypogonadism 24 without anosmia
- wdr-62 [Browse genome (BioProject PRJNA13758)] [Search on AGR]
Caenorhabditis elegans Predicted to enable kinase activity. Predicted to be involved in centriole replication. Predicted to be located in mitotic spindle. Human ortholog(s) of this gene implicated in several diseases, including nephronophthisis 20; polymicrogyria; and primary autosomal recessive microcephaly 2 with or without cortical malformations. Is an ortholog of human WDR62 (WD repeat domain 62).
- D1037.1 [Browse genome (BioProject PRJNA13758)] [Search on AGR]
Caenorhabditis elegans Predicted to enable RNA binding activity. Predicted to be involved in regulation of mRNA splicing, via spliceosome. Human ortholog(s) of this gene implicated in congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay. Is an ortholog of human SON (SON DNA and RNA binding protein).
- FEZF1-AS1 [Search on AGR]
Homo sapiens ASSOCIATED WITH genetic disease; hypogonadotropic hypogonadism 22 with or without anosmia
- Mettl9 [Search on AGR]
Mus musculus PHENOTYPE: Mice exhibit reduced 1MH methylation without any abnormal phenotype. [provided by MGI curators]