PROM1
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 4[14]
- Cytogenetic location
- 4p15.32
- Encodes
- prominin 1, Prominin-1[11][12]
- Expressed in
- bronchial epithelial cell, nasal epithelium, parotid gland, mucosa of paranasal sinus, olfactory zone of nasal mucosa, trachea, pylorus, renal medulla, mucosa of colon, mucosa of sigmoid colon
- Found in taxon
- Homo sapiens[13]
- Genetic association
- Dental caries, retinitis pigmentosa 41, cone-rod dystrophy 12, cone-rod dystrophy[15][16][17][18]
- HomoloGene ID
- 4390[3]
- Strand orientation
- reverse strand[19]
🏷️ Also known as
en AC133
en CD133
en CORD12
en MCDR2
en MSTP061
en PROM1
en prominin 1
en PROML1
en RP41
en STGD4
🔖 Identifiers · 11
- CIViC gene ID
- 7014
- Ensembl gene ID
- ENSG00000007062
- Ensembl transcript ID
- ENST00000540805, ENST00000447510, ENST00000502501, ENST00000502943, ENST00000503884, ENST00000504842, ENST00000505450, ENST00000508167, ENST00000508322, ENST00000508940, ENST00000510224, ENST00000511153, ENST00000511270, ENST00000512304, ENST00000513108, ENST00000513448, ENST00000513946, ENST00000514693, ENST00000514967, ENST00000539194, ENST00000675377, ENST00000675613
- Entrez Gene ID
- 8842
- Exact match
- identifiers.org
- Freebase ID
- /m/02ps0py
- HGNC ID
- 9454
- HGNC gene symbol
- PROM1
- OMIM ID
- 604365
- RefSeq RNA ID
- NM_001145847, NM_001145848, NM_001145849, NM_001145850, NM_001145851, NM_001145852, NM_006017, XM_005248195, XM_005248196, XM_006713974, XM_011513893, XM_011513894, XM_011513895, XM_011513897, XM_011513900, XM_011513902, XM_011513903, XM_017008800, NM_001371406, NM_001371407, NM_001371408, XM_047416370, XM_047416372, XM_047416373, XM_047416374, XM_047416375, XM_047416376, XM_047416377, XM_047416378, XM_047416379
- UMLS CUI
- C1418946
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