TFCP2L1
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 2[11]
- Cytogenetic location
- 2q14.2[14]
- Encodes
- Transcription factor CP2 like 1[9]
- Expressed in
- parotid gland, minor salivary glands, renal medulla, human kidney, nasal epithelium, right lobe of thyroid gland, buccal mucosa cell, left lobe of thyroid gland, skin of thigh, rectum[15][16][17][18][19][20][21][22][23][24]
- Found in taxon
- Homo sapiens[10]
- Genetic association
- Behçet's disease[12]
- HomoloGene ID
- 8730[3]
- Strand orientation
- reverse strand[13]
🏷️ Also known as
en CRTR1
en LBP-9
en LBP9
en TFCP2L1
en transcription factor CP2 like 1
en transcription factor CP2-like 1
🔖 Identifiers · 9
- Ensembl gene ID
- ENSG00000115112
- Ensembl transcript ID
- ENST00000464621, ENST00000263707
- Entrez Gene ID
- 29842
- Exact match
- identifiers.org
- HGNC ID
- 17925
- HGNC gene symbol
- TFCP2L1
- OMIM ID
- 609785
- RefSeq RNA ID
- NM_014553, XM_017003902, XM_017003903, XM_017003904, XM_017003905, XM_047444020, XM_047444021
- UMLS CUI
- C1425181
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