Terminology Service for NFDI4Health
All terms in RGD
| Label | Id | Description |
|---|---|---|
| LOC685434 | rgd:1593823 | |
| Evi2a | rgd:1593824 | [ASSOCIATED WITH Developmental Disabilities (ortholog); epilepsy (ortholog); neurofibromatosis 1 (ortholog); FOUND IN integral component of membrane (inferred); INTERACTS WITH 6-propyl-2-thiouracil; bisphenol A; copper atom] |
| LOC685431 | rgd:1593825 | |
| LOC685427 | rgd:1593829 | |
| LOC100910744 | rgd:6497117 | [ENCODES a protein that exhibits G protein-coupled receptor activity (inferred); INVOLVED IN detection of chemical stimulus involved in sensory perception of smell (inferred); FOUND IN integral component of membrane (inferred); plasma membrane (inferred)] |
| Oas1g | rgd:6497100 | [ENCODES a protein that exhibits ATP binding (inferred); INVOLVED IN immune response (inferred); FOUND IN integral component of membrane (inferred)] |
| LOC108348505 | rgd:11386194 | |
| LOC103690535 | rgd:9372171 | |
| LOC100912334 | rgd:6487798 | |
| LOC685443 | rgd:1593814 | |
| LOC685441 | rgd:1593816 | |
| Nek5 | rgd:1593817 | [ENCODES a protein that exhibits protein kinase activity (ortholog); INVOLVED IN positive regulation of cysteine-type endopeptidase activity (ortholog); positive regulation of striated muscle cell differentiation (ortholog); ASSOCIATED WITH Chromosome 13q Deletion Syndrome (ortholog); chromosome 13q14 deletion syndrome (ortholog); intellectual disability (ortholog); INTERACTS WITH bisphenol A; furan; 4,4'-sulfonyldiphenol (ortholog)] |
| LOC100912333 | rgd:6487791 | |
| LOC103690631 | rgd:9372178 | |
| LOC685438 | rgd:1593819 | |
| LOC103692123 | rgd:9372179 | |
| LOC108349259 | rgd:11488394 | |
| LOC102553697 | rgd:7584717 | |
| LOC102555246 | rgd:7643619 | |
| LOC103694817 | rgd:9215300 |