SLCO1B3 - Gene browser | 3billion

SLCO1B3

SLCO1B3

solute carrier organic anion transporter family member 1B3

HCNC Approved Symbol: SLCO1B3 (HGNC:10961)
Genomic Coordinates: 12:20,810,705 - 20,916,911 (12p12.2)
Synonyms: OATP8, OATP1B3, SLC21A8
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

1Patient

In total, 1 patient was diagnosed with a variant in the SLCO1B3 gene.

Frequently observed phenotypes(Top 5 only)

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

01
Patient count

Direct hyperbilirubinemia: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Increased alanine aminotransferase: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Jaundice: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)

Last updated: 2024-06-30

SLCO1B3 - Gene browser | 3billion