GDAP1 - Gene browser

GDAP1

ganglioside induced differentiation associated protein 1

HCNC Approved Symbol: GDAP1 (HGNC:15968)
Genomic Coordinates: 8:74,350,403 - 74,488,872 (8q21.11)
Synonyms: CMT4, CMT2K, CMT4A
Disease Associations: This gene is associated with the following 4 diseases in OMIM.

25Patients

In total, 25 patients were diagnosed with a variant in the GDAP1 gene.

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

025
Patient count

Muscle weakness: 9 (36.0%)
Patient Count: 9 (36.0%)
% of total patients presenting each phenotype is shown in parentheses.
9 (36.0%)
Peripheral axonal degeneration: 6 (24.0%)
Patient Count: 6 (24.0%)
% of total patients presenting each phenotype is shown in parentheses.
6 (24.0%)
Charcot arthropathy: 5 (20.0%)
Patient Count: 5 (20.0%)
% of total patients presenting each phenotype is shown in parentheses.
5 (20.0%)
Peripheral neuropathy: 4 (16.0%)
Patient Count: 4 (16.0%)
% of total patients presenting each phenotype is shown in parentheses.
4 (16.0%)
Distal muscle weakness: 4 (16.0%)
Patient Count: 4 (16.0%)
% of total patients presenting each phenotype is shown in parentheses.
4 (16.0%)