- rft-1 [Browse genome (BioProject PRJNA13758)] [Search on AGR]
Caenorhabditis elegans Enables riboflavin transmembrane transporter activity. Involved in embryo development. Predicted to be located in plasma membrane. Human ortholog(s) of this gene implicated in several diseases, including Brown-Vialetto-Van Laere syndrome 1; Brown-Vialetto-Van Laere syndrome 2; and Fazio-Londe disease. Is an ortholog of human SLC52A2 (solute carrier family 52 member 2) and SLC52A3 (solute carrier family 52 member 3).
- rft-2 [Browse genome (BioProject PRJNA13758)] [Search on AGR]
Caenorhabditis elegans Enables riboflavin transmembrane transporter activity. Involved in IRE1-mediated unfolded protein response. Predicted to be located in plasma membrane. Human ortholog(s) of this gene implicated in several diseases, including Brown-Vialetto-Van Laere syndrome 1; Brown-Vialetto-Van Laere syndrome 2; and Fazio-Londe disease. Is an ortholog of human SLC52A1 (solute carrier family 52 member 1); SLC52A2 (solute carrier family 52 member 2); and SLC52A3 (solute carrier family 52 member 3).
- Fam193a [Search on AGR]
Homo sapiens ASSOCIATED WITH cherubism; Ellis-Van Creveld syndrome; INTERACTS WITH 17beta-hydroxy-5alpha-androstan-3-one; acrolein; Aflatoxin B2 alpha
- Mroh6 [Search on AGR]
Homo sapiens ASSOCIATED WITH Arrhinencephaly; Brown-Vialetto-Van Laere syndrome 2; epidermolysis bullosa simplex with muscular dystrophy; INTERACTS WITH 17beta-estradiol; aflatoxin B1; all-trans-retinoic acid
- Mroh1 [Search on AGR]
Homo sapiens ASSOCIATED WITH Arrhinencephaly; Brown-Vialetto-Van Laere syndrome 2; epidermolysis bullosa simplex with muscular dystrophy; INTERACTS WITH 2,2',4,4'-Tetrabromodiphenyl ether; 2,4,6-tribromophenol; 2-palmitoylglycerol
- Hgh1 [Search on AGR]
Homo sapiens ASSOCIATED WITH Arrhinencephaly; Brown-Vialetto-Van Laere syndrome 2; epidermolysis bullosa simplex with muscular dystrophy; INTERACTS WITH (-)-alpha-phellandrene; 3-isobutyl-1-methyl-7H-xanthine; acrylamide
- Ccdc166 [Search on AGR]
Homo sapiens ASSOCIATED WITH Arrhinencephaly; Brown-Vialetto-Van Laere syndrome 2; epidermolysis bullosa simplex with muscular dystrophy; INTERACTS WITH benzo[a]pyrene; bis(2-ethylhexyl) phthalate; perfluorohexanesulfonic acid
- Crabp2 [Search on AGR]
Homo sapiens This gene encodes a member of the retinoic acid (RA, a form of vitamin A) binding protein family and lipocalin/cytosolic fatty-acid binding protein family. The protein is a cytosol-to-nuclear shuttling protein, which facilitates RA binding to its cognate receptor complex and transfer to the nucleus. It is involved in the retinoid signaling pathway, and is associated with increased circulating low-density lipoprotein cholesterol. Alternatively spliced transcript variants encoding the same protein have been found for this gene.[provided by RefSeq, Dec 2010]
- Evc [Search on AGR]
Homo sapiens This gene encodes a protein containing a leucine zipper and a transmembrane domain. This gene has been implicated in both Ellis-van Creveld syndrome (EvC) and Weyers acrodental dysostosis. [provided by RefSeq, Jul 2008]