WNT10B wt Allele

Preferred Label : WNT10B wt Allele;

NCIt synonyms : WNT12; WNT-12; Wingless-Type MMTV Integration Site Family, Member 10B Gene; STHAG8; SHFM6; Wnt Family Member 10B wt Allele;

NCIt definition : Human WNT10B wild-type allele is located in the vicinity of 12q13 and is approximately 6 kb in length. This allele, which encodes protein wnt-10b, is involved in the modulation of both adipogenesis and cellular fates during development.;

GenBank Accession Number : NM_003394;

Details

Origin ID

C52979;

UMLS CUI

C1710649;

Automatic exact mappings (from CISMeF team)
- Split-hand/foot malformation 6 [OMIM Phenotype]
- Tooth agenesis, selective, 8 [OMIM Phenotype]
- Wnt family member 10B [ORDO Gene]
- split hand-foot malformation 6 [DO Concept]
OMIM relation
- Wingless-type mmtv integration site family, member 10b [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_associated_with_disease
- Breast Carcinoma [NCIt concept]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 12q13 [NCIt concept]
gene_is_element_in_pathway
- Basal Cell Carcinoma 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
- Adipogenesis [NCIt concept]
- Cell Differentiation Process [NCIt concept]
- Intercellular Communication Process [NCIt concept]
- Signal Transduction [NCIt concept]

Keyword's position in hierarchy(ies) :

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