UGT1A1
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 2[26]
- Cytogenetic location
- 2q37.1[31]
- Expressed in
- duodenum, right lobe of liver, testicle, mucosa of transverse colon, human kidney, rectum, urinary bladder, renal cortex, gallbladder, olfactory zone of nasal mucosa[32][33][34][35][36][37][38][39][40][41]
- Found in taxon
- Homo sapiens[25]
- Genetic association
- Gilbert syndrome, Lucey–Driscoll syndrome, Crigler-Najjar syndrome type 2[27][28][29]
- HomoloGene ID
- 128034[3]
- Ortholog
- Ugt1a1, Ugt1a1, ugt1a5, ugt1a2, ugt1ab, ugt1b5, ugt1a6, ugt1b1, ugt1a7, ugt1b3, ugt1b7, Ugt301D1, ugt1b4, ugt1a4, ugt1b2, ugt1a1[10][11][12][13][14][15][16][17][18][19][20][21][22][23]
- Strand orientation
- forward strand[30]
🏷️ Also known as
en BILIQTL1
en GNT1
en HUG-BR1
en UDP glucuronosyltransferase family 1 member A1
en UDPGT
en UDPGT 1-1
en UGT1
en UGT1A
en UGT1A1
ja グルクロン酸転移酵素
🔖 Identifiers · 12
- CIViC gene ID
- 12422
- Ensembl gene ID
- ENSG00000241635
- Ensembl transcript ID
- ENST00000360418, ENST00000305208
- Entrez Gene ID
- 54658
- Exact match
- identifiers.org
- Freebase ID
- /m/02p9dwx
- HGNC ID
- 12530
- HGNC gene symbol
- UGT1A1
- Microsoft Academic ID (discontinued)
- 2779131365
- OMIM ID
- 191740
- RefSeq RNA ID
- NM_000463
- UMLS CUI
- C0537026
🔗 Connections
Expressed in 6
← Genetic association 3
Genetic association 2
Chromosome 1
Found in taxon 1
Instance of 1
Press Enter · cited answer in seconds