POC1B
protein-coding gene in the species Homo sapiens
Facts
12 properties- Instance of
- gene
- Chromosome
- human chromosome 12[9]
- Cytogenetic location
- 12q21.33[13]
- Encodes
- POC1 centriolar protein B[7]
- Expressed in
- pancreatic epithelial cell, sperm, corpus callosum, secondary oocyte, epithelium of nasopharynx, endometrium, pancreatic ductal cell, Achilles tendon, epithelium of colon, mucosa of paranasal sinus[14][15][16][17][18][19][20][21][22][23]
- Found in taxon
- Homo sapiens[8]
- Genetic association
- cone-rod dystrophy 20, cone-rod dystrophy[10][11]
- HomoloGene ID
- 41728[1]
- Strand orientation
- reverse strand[12]
🏷️ Also known as
en CORD20
en PIX1
en POC1B
en POC1 centriolar protein B
en TUWD12
en WDR51B
🔖 Identifiers · 9
- Ensembl gene ID
- ENSG00000139323
- Ensembl transcript ID
- ENST00000552563, ENST00000313546, ENST00000393179, ENST00000539190, ENST00000546740, ENST00000546830, ENST00000547274, ENST00000547496, ENST00000548715, ENST00000549035, ENST00000549304, ENST00000549504, ENST00000549591, ENST00000551819
- Entrez Gene ID
- 282809
- Exact match
- identifiers.org
- HGNC ID
- 30836
- HGNC gene symbol
- POC1B
- OMIM ID
- 614784
- RefSeq RNA ID
- NR_037660, NM_001199777, NM_172240, NR_037659
- UMLS CUI
- C1538096
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