WNT2 wt Allele

Preferred Label : WNT2 wt Allele;

NCIt synonyms : Wnt Family Member 2 wt Allele; Wingless-Type MMTV Integration Site Family Member 2 Gene; IRP; INT1L1;

NCIt definition : Human WNT2 wild-type allele is located in the vicinity of 7q31 and is approximately 46 kb in length. This allele, which encodes protein wnt-2, plays a role in embryonic development. Deletion of this gene may be involved in autism.;

GenBank Accession Number : NM_003391;

Détails

Origin ID

C52990;

UMLS CUI

C1710653;

Automatic exact mappings (from CISMeF team)
- Wingless-type mmtv integration site family, member 2 [OMIM gene]
- iron-regulatory proteins [MeSH Descriptor]
OMIM relation
- Wingless-type mmtv integration site family, member 2 [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_associated_with_disease
- Malignant Breast Neoplasm [NCIt concept]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 7q31 [NCIt concept]
gene_is_element_in_pathway
- Basal Cell Carcinoma Pathway [NCIt concept]
- Hippo Signaling Pathway [NCIt concept]
- Melanogenesis Pathway [NCIt concept]
- WNT Signaling Pathway BioCarta [NCIt concept]
- Wnt Signaling Pathway KEGG [NCIt concept]
- mTOR Signaling Pathway KEGG [NCIt concept]
gene_plays_role_in_process
- Cell Proliferation [NCIt concept]
- Intercellular Communication Process [NCIt concept]
- Pattern Formation [NCIt concept]
- Signal Transduction [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

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