SLCO1B1 - Gene browser

SLCO1B1

solute carrier organic anion transporter family member 1B1

HCNC Approved Symbol: SLCO1B1 (HGNC:10959)
Genomic Coordinates: 12:21,131,194 - 21,239,796 (12p12.1)
Synonyms: OATP-C, LST-1, OATP1B1, SLC21A6
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

6Patients

In total, 6 patients were diagnosed with a variant in the SLCO1B1 gene.

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

06
Patient count

Conjugated hyperbilirubinemia: 3 (50.0%)
Patient Count: 3 (50.0%)
% of total patients presenting each phenotype is shown in parentheses.
3 (50.0%)
Direct hyperbilirubinemia: 3 (50.0%)
Patient Count: 3 (50.0%)
% of total patients presenting each phenotype is shown in parentheses.
3 (50.0%)
Jaundice: 2 (33.3%)
Patient Count: 2 (33.3%)
% of total patients presenting each phenotype is shown in parentheses.
2 (33.3%)
Hypercholesterolemia: 1 (16.7%)
Patient Count: 1 (16.7%)
% of total patients presenting each phenotype is shown in parentheses.
1 (16.7%)
Obesity: 1 (16.7%)
Patient Count: 1 (16.7%)
% of total patients presenting each phenotype is shown in parentheses.
1 (16.7%)