WNT10B
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 12[12]
- Cytogenetic location
- 12q13.12[15]
- Encodes
- Wnt family member 10B[10]
- Expressed in
- orbitofrontal cortex, nucleus accumbens, Brodmann area 10, Region I of hippocampus proper, cingulate gyrus, anterior cingulate cortex, Brodmann area 46, right frontal lobe, dorsolateral prefrontal cortex, entorhinal cortex[16][17][18][19][20][21][22][23][24][25]
- Found in taxon
- Homo sapiens[11]
- Genetic association
- split hand-foot malformation 2[13]
- HomoloGene ID
- 20721[3]
- Strand orientation
- reverse strand[14]
🏷️ Also known as
en SHFM6
en STHAG8
en WNT10B
en WNT-12
en Wnt family member 10B
ar WNT١٠B
🔖 Identifiers · 10
- Ensembl gene ID
- ENSG00000169884
- Ensembl transcript ID
- ENST00000475740, ENST00000301061, ENST00000403957, ENST00000407467, ENST00000413630, ENST00000420388
- Entrez Gene ID
- 7480
- Exact match
- identifiers.org
- Freebase ID
- /m/02kg6fk
- HGNC ID
- 12775
- HGNC gene symbol
- WNT10B
- OMIM ID
- 601906
- RefSeq RNA ID
- NM_003394
- UMLS CUI
- C1421511
🔗 Connections
Expressed in 8
Chromosome 1
Found in taxon 1
Instance of 1
← Genetic association 1
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