RRAD wt Allele

Preferred Label : RRAD wt Allele;

NCIt synonyms : RAS (RAD and GEM) Like GTP Binding 3 Gene; RAD Gene; RAD1; RAD; REM3; Ras Gene Associated with Diabetes; RRAD, Ras Related Glycolysis Inhibitor and Calcium Channel Regulator wt Allele; Ras-Related Associated with Diabetes Gene;

NCIt definition : Human RRAD wild-type allele is located in the vicinity of 16q22 and is approximately 4 kb in length. This allele, which encodes GTP-binding protein RAD, may play a role in the mediation of the cellular response to insulin. The wild-type allele is expressed at elevated levels in patients with non-insulin resistant diabetes mellitus.;

GenBank Accession Number : NM_004165;

Details

Origin ID

C52601;

UMLS CUI

C1705625;

Automatic exact mappings (from CISMeF team)
- Dyschromatosis symmetrica hereditaria [OMIM Phenotype]
- ERCC excision repair 4, endonuclease catalytic subunit [ORDO Gene]
- RAD9-HUS1-RAD1 interacting nuclear orphan 1 [HGNC gene]
- Rad1 checkpoint dna exonuclease [OMIM gene]
- Radiology [LOINC Class]
- Radiology studies [LOINC component]
- Right axis deviation [HPO term]
- Rrad ras-related glycolysis inhibitor and calcium channel regulator [OMIM gene]
- ribosome-associated ubiquitin-dependent protein catabolic process [GO term]
Currated CISMeF NLP mapping
- rad [IUPAC Unit]
- rad (qualifier value) [SNOMED CT concept]
OMIM relation
- Rrad ras-related glycolysis inhibitor and calcium channel regulator [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
concept_is_in_subset
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 16q22 [NCIt concept]
gene_plays_role_in_process
- GTP Binding [NCIt concept]
- Hydrolysis [NCIt concept]
- Signal Transduction [NCIt concept]

Keyword's position in hierarchy(ies) :

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