RFX5
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 1[12]
- Cytogenetic location
- 1q21.3[15]
- Encodes
- Regulatory factor X5, DNA-binding protein RFX5[9][10]
- Expressed in
- epithelium of nasopharynx, lymph node, monocyte, appendix, granulocyte, right adrenal cortex, rectum, tonsil, spleen, pons[16][17][18][19][20][21][22][23][24][25]
- Found in taxon
- Homo sapiens[11]
- Genetic association
- bare lymphocyte syndrome 2[13]
- HomoloGene ID
- 388[3]
- Strand orientation
- reverse strand[14]
🏷️ Also known as
en regulatory factor X5
en RFX5
ar RFX٥
🔖 Identifiers · 11
- Ensembl gene ID
- ENSG00000143390
- Ensembl transcript ID
- ENST00000494217, ENST00000290524, ENST00000368870, ENST00000392746, ENST00000412774, ENST00000421986, ENST00000422595, ENST00000430227, ENST00000435314, ENST00000436271, ENST00000436637, ENST00000437327, ENST00000444392, ENST00000450506, ENST00000452456, ENST00000452671, ENST00000458484, ENST00000469513, ENST00000475144, ENST00000478564, ENST00000479681
- Entrez Gene ID
- 5993
- Exact match
- identifiers.org
- Freebase ID
- /m/03gxl3z
- HGNC ID
- 9986
- HGNC gene symbol
- RFX5
- Microsoft Academic ID (discontinued)
- 2780353945
- OMIM ID
- 601863
- RefSeq RNA ID
- XM_011509850, NM_000449, NM_001025603, XM_005245405, XM_005245406, XM_011509847, XM_011509848, XM_011509849, XM_017001999, XM_017002000, XM_024448791
- UMLS CUI
- C1419363
🔗 Connections
Expressed in 8
Chromosome 1
Found in taxon 1
Instance of 1
← Genetic association 1
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