Annotation Detail
Information
- Associated Genes
- UGT1A1
- Associated Variants
-
UGT1A6 c.862-6500T>A, UGT1A5 c.868-6500T>A, UGT1A9 c.856-6500T>A, UGT1A7 c.856-6500T>A, UGT1A4 c.868-6500T>A, UGT1A8 c.856-6500T>A, UGT1A10 c.856-6500T>A, UGT1A3 c.868-6500T>A, UGT1A1 p.Phe83Ile (p.F83I)
(
ENST00000344644.10,
ENST00000373445.1,
ENST00000373450.5,
ENST00000373426.4,
ENST00000305139.11,
ENST00000373424.5,
ENST00000406651.1,
ENST00000373414.4,
ENST00000354728.5,
ENST00000373409.8,
ENST00000305208.10,
ENST00000360418.4,
ENST00000482026.6 )
UGT1A6 c.862-6500T>C, UGT1A5 c.868-6500T>C, UGT1A9 c.856-6500T>C, UGT1A7 c.856-6500T>C, UGT1A4 c.868-6500T>C, UGT1A8 c.856-6500T>C, UGT1A10 c.856-6500T>C, UGT1A3 c.868-6500T>C, UGT1A1 p.Phe83Leu (p.F83L) ( ENST00000344644.10, ENST00000373445.1, ENST00000373450.5, ENST00000373426.4, ENST00000305139.11, ENST00000373424.5, ENST00000406651.1, ENST00000373414.4, ENST00000354728.5, ENST00000373409.8, ENST00000305208.10, ENST00000360418.4, ENST00000482026.6 )
UGT1A6 c.862-6500T>A, UGT1A5 c.868-6500T>A, UGT1A9 c.856-6500T>A, UGT1A7 c.856-6500T>A, UGT1A4 c.868-6500T>A, UGT1A8 c.856-6500T>A, UGT1A10 c.856-6500T>A, UGT1A3 c.868-6500T>A, UGT1A1 p.Phe83Ile (p.F83I) ( ENST00000344644.10, ENST00000373445.1, ENST00000373450.5, ENST00000373426.4, ENST00000305139.11, ENST00000373424.5, ENST00000406651.1, ENST00000373414.4, ENST00000354728.5, ENST00000373409.8, ENST00000305208.10, ENST00000360418.4, ENST00000482026.6 )
UGT1A6 c.862-6500T>C, UGT1A5 c.868-6500T>C, UGT1A9 c.856-6500T>C, UGT1A7 c.856-6500T>C, UGT1A4 c.868-6500T>C, UGT1A8 c.856-6500T>C, UGT1A10 c.856-6500T>C, UGT1A3 c.868-6500T>C, UGT1A1 p.Phe83Leu (p.F83L) ( ENST00000344644.10, ENST00000373445.1, ENST00000373450.5, ENST00000373426.4, ENST00000305139.11, ENST00000373424.5, ENST00000406651.1, ENST00000373414.4, ENST00000354728.5, ENST00000373409.8, ENST00000305208.10, ENST00000360418.4, ENST00000482026.6 ) - Associated Disease
- Gilbert Disease (disorder)
- Source Database
- DisGeNET
- Description
- Novel missense mutation of the UGT1A1 gene in Thai siblings with Gilbert's syndrome.
- Pubmed
- 12139570
- Original source reporting the Gene Disease association
- UNIPROT
- DisGENET score for the Gene Disease association
- 0.29501695686041
- Year of publication
- 2002
Drugs