TCF12
protein-coding gene in the species Homo sapiens
Facts
12 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 15
- Cytogenetic location
- 15q21.3
- Encodes
- Transcription factor 12[9]
- Expressed in
- periodontal fiber, ventricular zone, ganglionic eminence, hair follicle, epithelium of colon, Achilles tendon, stromal cell of endometrium, corpus callosum, optic nerve, mucosa of paranasal sinus
- Found in taxon
- Homo sapiens[10]
- HomoloGene ID
- 40774[3]
- Strand orientation
- forward strand
🏷️ Also known as
en transcription factor 12
en bHLHb20
en CRS3
en HEB
en HH26
en HsT17266
en HTF4
en p64
en TCF-12
en TCF12
ar TCF١٢
🔖 Identifiers · 10
- Ensembl gene ID
- ENSG00000140262
- Ensembl transcript ID
- ENST00000569880, ENST00000267811, ENST00000333725, ENST00000343827, ENST00000438423, ENST00000537840, ENST00000543579, ENST00000557843, ENST00000557947, ENST00000558210, ENST00000558908, ENST00000559216, ENST00000559609, ENST00000559703, ENST00000559710, ENST00000560190, ENST00000560191, ENST00000560506, ENST00000560764, ENST00000560836, ENST00000560887, ENST00000560948, ENST00000561152, ENST00000561235, ENST00000561346, ENST00000561420, ENST00000561449, ENST00000561454
- Entrez Gene ID
- 6938
- Exact match
- identifiers.org
- Freebase ID
- /m/03gx23h
- HGNC ID
- 11623
- HGNC gene symbol
- TCF12
- OMIM ID
- 600480
- RefSeq RNA ID
- XM_011521969, NM_001306219, NM_001306220, NM_003205, NM_207036, NM_207037, NM_207038, NM_207040, XM_011521959, XM_011521960, XM_011521961, XM_011521962, XM_011521963, XM_011521966, NM_001322151, NM_001322152, NM_001322154, NM_001322156, NM_001322157, NM_001322158, NM_001322159, NM_001322161, NM_001322162, NM_001322164, NM_001322165, XM_017022520, XM_047432971, XM_047432972, XM_047432973, XM_047432974, XM_047432975, XM_047432976, XM_047432977, XM_047432978
- UMLS CUI
- C1420632
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