Terminology Service for NFDI4Health
All terms in RGD
| Label | Id | Description |
|---|---|---|
| Dnaaf3 | rgd:2323487 | [INVOLVED IN axonemal dynein complex assembly (ortholog); determination of left/right symmetry (ortholog); heart development (ortholog); ASSOCIATED WITH cardiomyopathy (ortholog); Ciliary Motility Disorders (ortholog); dilated cardiomyopathy (ortholog); FOUND IN cytoplasm (inferred); INTERACTS WITH 1-naphthyl isothiocyanate; bisphenol A; amiodarone (ortholog)] |
| LOC100359752 | rgd:2323488 | [ASSOCIATED WITH chromosome 18q deletion syndrome (ortholog); Neurodevelopmental Disorders (ortholog); INTERACTS WITH tebuconazole (ortholog)] |
| LOC103692179 | rgd:9124640 | |
| Elovl1 | rgd:1587151 | [ENCODES a protein that exhibits fatty acid elongase activity (ortholog); INVOLVED IN ceramide biosynthetic process (ortholog); establishment of skin barrier (ortholog); fatty acid elongation, monounsaturated fatty acid (ortholog); ASSOCIATED WITH Charcot-Marie-Tooth disease dominant intermediate C (ortholog); ICHTHYOTIC KERATODERMA, SPASTICITY, HYPOMYELINATION, AND DYSMORPHIC FACIAL FEATURES (ortholog); FOUND IN endoplasmic reticulum (ortholog); INTERACTS WITH 6-propyl-2-thiouracil; bisphenol A; dibutyl phthalate] |
| LOC100359760 | rgd:2323480 | |
| LOC100359754 | rgd:2323486 | |
| LOC102557601 | rgd:7496505 | |
| LOC100359763 | rgd:2323477 | |
| Awat1 | rgd:1587163 | [ENCODES a protein that exhibits long-chain-alcohol O-fatty-acyltransferase activity (ortholog); PARTICIPATES IN retinol metabolic pathway; vitamin A deficiency pathway; ASSOCIATED WITH autistic disorder (ortholog); syndromic X-linked intellectual disability Lubs type (ortholog); INTERACTS WITH bisphenol A; copper atom; copper(0)] |
| LOC679519 | rgd:1587164 | |
| LOC679514 | rgd:1587169 | |
| LOC100359768 | rgd:2323472 | |
| LOC100359767 | rgd:2323473 | |
| LOC100910807 | rgd:6496755 | [ENCODES a protein that exhibits nucleic acid binding (inferred)] |
| LOC100910812 | rgd:6496783 | |
| LOC102555442 | rgd:7496510 | |
| Tmem249 | rgd:6496784 | [ASSOCIATED WITH autosomal recessive limb-girdle muscular dystrophy type 2Q (ortholog); Brown-Vialetto-Van Laere Syndrome 2 (ortholog); epidermolysis bullosa simplex Ogna type (ortholog); INTERACTS WITH rotenone (ortholog); silicon dioxide (ortholog); valproic acid (ortholog)] |
| LOC103694939 | rgd:9089892 | |
| LOC103694670 | rgd:9089891 | |
| LOC108353796 | rgd:11402924 |