WNT10A
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 2[12]
- Cytogenetic location
- 2q35[17]
- Encodes
- Wnt family member 10A[10]
- Expressed in
- gonad, bone marrow cell, skin of abdomen, skin of leg, granulocyte, lymph node, pituitary gland, mucosa of transverse colon, olfactory zone of nasal mucosa, anterior pituitary[18][19][20][21][22][23][24][25][26][27]
- Found in taxon
- Homo sapiens[11]
- Genetic association
- Odonto-onycho-dermal dysplasia, Schöpf–Schulz–Passarge syndrome, tooth agenesis[13][14][15]
- HomoloGene ID
- 22525[3]
- Strand orientation
- forward strand[16]
🏷️ Also known as
en STHAG4
en OODD
en SSPS
en WNT10A
en Wnt family member 10A
ar WNT١٠A
vi Gen WNT10A
🔖 Identifiers · 10
- Ensembl gene ID
- ENSG00000135925
- Ensembl transcript ID
- ENST00000489887, ENST00000258411, ENST00000458582, ENST00000483911
- Entrez Gene ID
- 80326
- Exact match
- identifiers.org
- Freebase ID
- /m/02kgp92
- HGNC ID
- 13829
- HGNC gene symbol
- WNT10A
- OMIM ID
- 606268
- RefSeq RNA ID
- XM_011511930, NM_025216, XM_011511929
- UMLS CUI
- C1422222
🔗 Connections
Expressed in 5
Chromosome 1
Found in taxon 1
Genetic association 1
Instance of 1
← Genetic association 1
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