rft-1

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

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).

M05D6.2

Caenorhabditis elegans

Predicted to be involved in signal transduction. Is an ortholog of human TCP11 (t-complex 11); TCP11L1 (t-complex 11 like 1); and TCP11L2 (t-complex 11 like 2).

GRHL3-AS1

Homo sapiens

ASSOCIATED WITH Van der Woude Syndrome 2

mam-1

Caenorhabditis elegans

Predicted to enable transmembrane signaling receptor activity. Predicted to be involved in regulation of T cell activation and regulation of T cell migration. Predicted to be located in membrane.

C35B8.3

Caenorhabditis elegans

Predicted to be located in mitochondrion. Is an ortholog of human TCAIM (T cell activation inhibitor, mitochondrial).

Fam193a

Homo sapiens

ASSOCIATED WITH cherubism; Ellis-Van Creveld syndrome; INTERACTS WITH 17beta-hydroxy-5alpha-androstan-3-one; acrolein; Aflatoxin B2 alpha

Hgh1

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

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

tbx-40

Caenorhabditis elegans

Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in cell fate specification and regulation of transcription by RNA polymerase II. Predicted to be located in chromatin and nucleus. Expressed in phasmid neurons. Human ortholog(s) of this gene implicated in Abruzzo-Erickson syndrome; X-linked cleft palate with or without ankyloglossia; and bone disease (multiple). Is an ortholog of several human genes including TBX15 (T-box transcription factor 15); TBX4 (T-box transcription factor 4); and TBX6 (T-box transcription factor 6).