RFXANK
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 19[13]
- Cytogenetic location
- 19p13.11[16]
- Encodes
- Regulatory factor X associated ankyrin containing protein, DNA-binding protein RFXANK[10][11]
- Expressed in
- mucosa of transverse colon, right uterine tube, right lobe of thyroid gland, ventricular zone, left lobe of thyroid gland, olfactory zone of nasal mucosa, granulocyte, canal of the cervix, apex of heart, right ovary[17][18][19][20][21][22][23][24][25][26]
- Found in taxon
- Homo sapiens[12]
- Genetic association
- bare lymphocyte syndrome 2[14]
- HomoloGene ID
- 2760[3]
- Strand orientation
- forward strand[15]
🏷️ Also known as
en ANKRA1
en BLS
en F14150_1
en regulatory factor X associated ankyrin containing protein
en RFXANK
en RFX-B
🔖 Identifiers · 11
- Ensembl gene ID
- ENSG00000064490
- Ensembl transcript ID
- ENST00000593273, ENST00000303088, ENST00000392324, ENST00000407360, ENST00000421262, ENST00000456252, ENST00000535017, ENST00000536253, ENST00000540977, ENST00000540981, ENST00000541873, ENST00000543118, ENST00000543157, ENST00000544923, ENST00000545522
- Entrez Gene ID
- 8625
- Exact match
- identifiers.org
- Freebase ID
- /m/03g_wvm
- HGNC ID
- 9987
- HGNC gene symbol
- RFXANK
- Microsoft Academic ID (discontinued)
- 2779792765
- OMIM ID
- 603200
- RefSeq RNA ID
- NM_001278727, NM_001278728, NM_003721, NM_134440, XM_005260134, XM_005260135, XM_005260137, NM_001370233, NM_001370234, NM_001370235, NM_001370236, NM_001370237, NM_001370238
- UMLS CUI
- C1419364
🔗 Connections
Expressed in 2
Chromosome 1
Found in taxon 1
Instance of 1
← Genetic association 1
Press Enter · cited answer in seconds