CHCHD2 - Gene browser | 3billion

CHCHD2

CHCHD2

coiled-coil-helix-coiled-coil-helix domain containing 2

HCNC Approved Symbol: CHCHD2 (HGNC:21645)
Genomic Coordinates: 7:56,101,573 - 56,106,476 (7p11.2)
Synonyms: MIX17B, MNRR1, C7orf17
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 CHCHD2 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

Parkinsonism: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Tremor: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Weight loss: 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

CHCHD2 - Gene browser | 3billion