ABCB11
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 2[12]
- Cytogenetic location
- 2q31.1[15]
- Expressed in
- right lobe of liver, testicle, mucosa of transverse colon, left testis, subcutaneous adipose tissue, right testis, olfactory zone of nasal mucosa, islet of Langerhans, gonad, ventricular zone[16][17][18][19][20][21][22][23][24][25]
- Found in taxon
- Homo sapiens[11]
- Genetic association
- metabolic disease[13]
- HomoloGene ID
- 74509[3]
- Strand orientation
- reverse strand[14]
🏷️ Also known as
en ABC16
en ABCB11
en ATP binding cassette subfamily B member 11
en BRIC2
en BSEP
en PFIC-2
en PFIC2
en PGY4
en SPGP
🔖 Identifiers · 12
- OpenAlex ID
- C2910800957
- Ensembl gene ID
- ENSG00000276582, ENSG00000073734
- Ensembl transcript ID
- ENST00000439188, ENST00000478354, ENST00000618180, ENST00000611248, ENST00000650372, ENST00000647920, ENST00000648875, ENST00000649448
- Entrez Gene ID
- 8647
- Exact match
- identifiers.org
- Freebase ID
- /m/02w1dq6
- HGNC ID
- 42
- HGNC gene symbol
- ABCB11
- Microsoft Academic ID (discontinued)
- 89571294
- OMIM ID
- 603201
- RefSeq RNA ID
- NM_003742, XM_006712817, XM_011512078, XM_011512080, XM_017005165, XM_017005166, XM_017005167
- UMLS CUI
- C1412070
🔗 Connections
Expressed in 3
Chromosome 1
Found in taxon 1
Genetic association 1
Instance of 1
← Genetic association 1
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