PITPNM3
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 17[14]
- Cytogenetic location
- 17p13.2-p13.1[17]
- Encodes
- PITPNM family member 3, PITPNM family member 3, Membrane-associated phosphatidylinositol transfer protein 3[11][12]
- Expressed in
- pancreatic ductal cell, endothelial cell, Brodmann area 23, spleen, cerebellar vermis, gingival epithelium, right hemisphere of cerebellum, prefrontal cortex, right frontal lobe, primary visual cortex[18][19][20][21][22][23][24][25][26][27]
- Found in taxon
- Homo sapiens[13]
- Genetic association
- cone-rod dystrophy 5[15]
- HomoloGene ID
- 66271[3]
- Strand orientation
- reverse strand[16]
🏷️ Also known as
en ACKR6
en CORD5
en NIR1
en PITPNM3
en PITPNM family member 3
en RDGBA3
🔖 Identifiers · 10
- Ensembl gene ID
- ENSG00000091622
- Ensembl transcript ID
- ENST00000576664, ENST00000262483, ENST00000421306, ENST00000572795, ENST00000575201
- Entrez Gene ID
- 83394
- Exact match
- identifiers.org
- Google Knowledge Graph ID
- /g/11gblf3tp5
- HGNC ID
- 21043
- HGNC gene symbol
- PITPNM3
- OMIM ID
- 608921
- RefSeq RNA ID
- XM_011524017, NM_001165966, NM_031220, XM_011524015, XM_011524016
- UMLS CUI
- C1427269
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