WNT7A
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 3[13]
- Cytogenetic location
- 3p25.1[17]
- Encodes
- Wnt family member 7A[11]
- Expressed in
- ventricular zone, ganglionic eminence, prefrontal cortex, gonad, right frontal lobe, cingulate gyrus, anterior cingulate cortex, amygdala, right lung, Brodmann area 9[18][19][20][21][22][23][24][25][26][27]
- Found in taxon
- Homo sapiens[12]
- Genetic association
- phocomelia, Schinzel type, Fuhrmann syndrome[14][15]
- HomoloGene ID
- 20969[3]
- Strand orientation
- reverse strand[16]
🏷️ Also known as
en Wnt-7a
en WNT7A
en Wnt family member 7A
ar WNT٧A
🔖 Identifiers · 11
- Ensembl gene ID
- ENSG00000154764
- Ensembl transcript ID
- ENST00000497808, ENST00000285018, ENST00000489346
- Entrez Gene ID
- 7476
- Exact match
- identifiers.org
- Freebase ID
- /m/02kfhlg
- HGNC ID
- 12786
- HGNC gene symbol
- WNT7A
- Microsoft Academic ID (discontinued)
- 2781052969
- OMIM ID
- 601570
- RefSeq RNA ID
- XM_011534091, NM_004625, XM_047448863
- UMLS CUI
- C1337005
🔗 Connections
Expressed in 7
Chromosome 1
Found in taxon 1
Instance of 1
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