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HSF4

heat shock transcription factor 4

HCNC Approved Symbol
HSF4 (HGNC:5227)
Genomic Coordinates
16:67,163,761 - 67,169,941 (16q22.1)
Synonyms
CTM
Disease Associations
This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

7Patients

In total, 7 patients were diagnosed with a variant in the HSF4 gene.

Frequently observed phenotypes

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

Cataract
 4 (57.1%)
Congenital cataract
 2 (28.6%)
Farsightedness
 
1 (14.3%)
Near sightedness
 
1 (14.3%)
Nystagmus
 
1 (14.3%)
HSF4 - Gene browser | 3billion