DCUN1D1 wt Allele

Preferred Label : DCUN1D1 wt Allele;

NCIt synonyms : DCN1, Defective in Cullin Neddylation 1, Domain Containing 1 Gene; SCRO; SCCRO; Defective in Cullin Neddylation 1 Domain Containing 1 wt Allele; Tes3; DCNL1; RP42; DCUN1L1; RP42 Homolog Gene; SCCRO1; DCN1; DCN1, Defective in Cullin Neddylation 1, Domain Containing 1 (S. cerevisiae) Gene; Squamous Cell Carcinoma Related Oncogene Gene; Squamous Cell Carcinoma-Related Oncogene 1 Gene;

NCIt definition : Human DCUN1D1 wild-type allele is located in the vicinity of 3q26.33 and is approximately 48 kb in length. This allele, which encodes DCN1-like protein 1, is involved in the regulation of ubiqitinylation by E3 cullin-RING ubiquitin ligase complexes.;

NCI Metathesaurus CUI : CL1412955;

GenBank Accession Number : AF292100;

Details

Origin ID

C175616;

UMLS CUI

C5443949;

Automatic exact mappings (from CISMeF team)
- Dcn1 domain-containing protein 1 [OMIM gene]
- Retinitis pigmentosa 42 [OMIM Phenotype]
- kelch like family member 7 [ORDO Gene]
- retinitis pigmentosa 42 [DO Concept]
OMIM relation
- Dcn1 domain-containing protein 1 [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_found_in_organism
- Human [NCIt concept]
gene_plays_role_in_process
- Ubiquitination [NCIt concept]

Keyword's position in hierarchy(ies) :

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