DCUN1D1 protein, human

Preferred Label : DCUN1D1 protein, human;

MeSH note : an intronless gene, RP42 maps to an autism susceptibility locus; orthologs from mouse & human; amino acid sequence in first source;

MeSH synonym : Tes3 protein, human; DCUN1L1 protein, human; DCN1 protein, human; RP42 protein, human; DCN1, defective in cullin neddylation 1, domain containing 1 protein, human; SSCRO protein, human; RP42 oncogene protein, human; SSC-related oncogene protein, human; DCNL1 protein, human; defective in cullin neddylation 1-like 1, human;

Is substance : O;

Details

Origin ID

C408631;

UMLS CUI

C0914516;

MeSH indexing information
- autistic disorder [MeSH Descriptor]
MeSH term(s) associated for indexing
- intracellular signaling peptides and proteins [MeSH Descriptor]
- proteins [MeSH Descriptor]
Record concept(s)
- DCUN1D1 protein, human [MeSH concept]
Semantic type(s)
- Amino Acid, Peptide, or Protein [UMLS semantic type]
- Biologically Active Substance [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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