WNT9B wt Allele

Preferred Label : WNT9B wt Allele;

NCIt synonyms : Wingless-Type MMTV Integration Site Family, Member 15 Gene; Wingless-Type MMTV Integration Site Family, Member 14 Gene; Wingless-Type MMTV Integration Site Family Member 9B Gene; Wnt Family Member 9B wt Allele; WNT15; WNT14B; Wingless-Type MMTV Integration Site Family, Member 9B Gene;

NCIt definition : Human WNT9B wild-type allele is located in the vicinity of 17q21.32 and is approximately 54 kb in length. This allele, which encodes protein Wnt-9b, is involved in signaling pathways that affect the development of craniofacial features and the urogenital system.;

NCIt note : Mutations in the WNT9B gene may be associated with familial prostate cancer. (JCO Precis Oncol. 2025; 9:e2400569.);

GenBank Accession Number : AF028703;

PubMed : 39874495;

Détails

Origin ID

C215065;

OMIM relation
- Wingless-type mmtv integration site family, member 9b [OMIM gene]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 17q21.32 [NCIt concept]
gene_is_element_in_pathway
- Alzheimer's Disease Pathway KEGG [NCIt concept]
- 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 Differentiation Process [NCIt concept]
- Cell Fate Control [NCIt concept]
- Intercellular Communication Process [NCIt concept]
- Morphogenesis [NCIt concept]
- Neural Development [NCIt concept]
- Signal Transduction [NCIt concept]

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

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