HSPB8 - Gene browser | 3billion

HSPB8

HSPB8

heat shock protein family B (small) member 8

HCNC Approved Symbol: HSPB8 (HGNC:30171)
Genomic Coordinates: 12:119,178,931 - 119,194,746 (12q24.23)
Synonyms: H11, E2IG1, HSP22, CMT2L
Disease Associations: This gene is associated with the following 2 diseases in OMIM.

Diagnosed Cases

1Patient

In total, 1 patient was diagnosed with a variant in the HSPB8 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

Absent achilles reflex: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Leg weakness: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Muscle atrophy: 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

HSPB8 - Gene browser | 3billion