CD46
protein-coding gene in the species Homo sapiens
Facts
11 properties- Chromosome
- human chromosome 1
- Cytogenetic location
- 1q32.2
- Encodes
- CD46 molecule, Membrane cofactor protein
- Expressed in
- palpebral conjunctiva, seminal vesicula, bronchial epithelial cell, jejunal mucosa, germinal epithelium, parotid gland, placenta, right uterine tube, right lung, body of pancreas
- Found in taxon
- Homo sapiens
- Genetic association
- obesity, atypical hemolytic-uremic syndrome with MCP/CD46 anomaly
- Genomic end
- 207795513, 207968858
- Genomic start
- 207925402, 207752037
- HomoloGene ID
- 7832[1]
- Strand orientation
- forward strand
🏷️ Also known as
en AHUS2
en CD46
en CD46 molecule
en MCP
en MIC10
en TLX
en TRA2.10
🔖 Identifiers · 9
- Ensembl gene ID
- ENSG00000117335
- Ensembl transcript ID
- ENST00000496723, ENST00000322875, ENST00000322918, ENST00000354848, ENST00000357714, ENST00000358170, ENST00000360212, ENST00000367041, ENST00000367042, ENST00000367047, ENST00000462968, ENST00000464082, ENST00000469535, ENST00000471987, ENST00000480003, ENST00000488596, ENST00000490278, ENST00000493796, ENST00000636114, ENST00000695777, ENST00000695778, ENST00000695780, ENST00000695790, ENST00000695783, ENST00000695785, ENST00000695786, ENST00000695784, ENST00000695781, ENST00000695789, ENST00000695779, ENST00000695788, ENST00000695782, ENST00000695787
- Entrez Gene ID
- 4179
- Exact match
- identifiers.org
- HGNC ID
- 6953
- HGNC gene symbol
- CD46
- OMIM ID
- 120920
- RefSeq RNA ID
- NM_002389, NM_153826, NM_172350, NM_172351, NM_172352, NM_172353, NM_172354, NM_172355, NM_172356, NM_172357, NM_172358, NM_172359, NM_172360, NM_172361, XM_011509563, XM_047420888, XM_047420894, XM_047420901, XM_047420909
- UMLS CUI
- C1824669
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