ABCC8 - Gene browser

ABCC8

ATP binding cassette subfamily C member 8

HCNC Approved Symbol: ABCC8 (HGNC:59)
Genomic Coordinates: 11:17,392,498 - 17,476,845 (11p15.1)
Synonyms: HI, PHHI, SUR1, MRP8, ABC36, HHF1, TNDM2, SUR, HRINS
Disease Associations: This gene is associated with the following 5 diseases in OMIM.

Diagnosed Cases

23Patients

In total, 23 patients were diagnosed with a variant in the ABCC8 gene.

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

023
Patient count

Hypoglycemia: 11 (47.8%)
Patient Count: 11 (47.8%)
% of total patients presenting each phenotype is shown in parentheses.
11 (47.8%)
Hyperinsulinemia: 7 (30.4%)
Patient Count: 7 (30.4%)
% of total patients presenting each phenotype is shown in parentheses.
7 (30.4%)
Hyperinsulinemic hypoglycemia: 6 (26.1%)
Patient Count: 6 (26.1%)
% of total patients presenting each phenotype is shown in parentheses.
6 (26.1%)
Hypoglycaemia: 4 (17.4%)
Patient Count: 4 (17.4%)
% of total patients presenting each phenotype is shown in parentheses.
4 (17.4%)
Hypoglycemic seizures: 4 (17.4%)
Patient Count: 4 (17.4%)
% of total patients presenting each phenotype is shown in parentheses.
4 (17.4%)