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ABCG5

ATP binding cassette subfamily G member 5

HCNC Approved Symbol
ABCG5 (HGNC:13886)
Genomic Coordinates
2:43,806,211 - 43,839,231 (2p21)
Synonyms
STSL
Disease Associations
This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

6Patients

In total, 6 patients were diagnosed with a variant in the ABCG5 gene.

Frequently observed phenotypes

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

Delayed milestones
 6 (100.0%)
ABCG5 - Gene browser | 3billion