RFXAP
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 13[11]
- Cytogenetic location
- 13q13.3[14]
- Expressed in
- gonad, tendon of biceps brachii, testicle, ventricular zone, palpebral conjunctiva, mucosa of paranasal sinus, gastric mucosa, cerebellar hemisphere, right hemisphere of cerebellum, ganglionic eminence[15][16][17][18][19][20][21][22][23][24]
- Found in taxon
- Homo sapiens[10]
- Genetic association
- bare lymphocyte syndrome 2[12]
- HomoloGene ID
- 452[3]
- Strand orientation
- forward strand[13]
🏷️ Also known as
en regulatory factor X associated protein
en RFXAP
🔖 Identifiers · 10
- Ensembl gene ID
- ENSG00000133111
- Ensembl transcript ID
- ENST00000472888, ENST00000255476
- Entrez Gene ID
- 5994
- Exact match
- identifiers.org
- Freebase ID
- /m/03h00d6
- HGNC ID
- 9988
- HGNC gene symbol
- RFXAP
- OMIM ID
- 601861
- RefSeq RNA ID
- NM_000538
- UMLS CUI
- C1419365
🔗 Connections
Expressed in 4
Chromosome 1
Found in taxon 1
Instance of 1
← Genetic association 1
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