3billion
back to listBack to List

TRIP4

thyroid hormone receptor interactor 4

HCNC Approved Symbol
TRIP4 (HGNC:12310)
Genomic Coordinates
15:64,387,836 - 64,455,303 (15q22.31)
Synonyms
HsT17391, ZC2HC5, ASC-1
Disease Associations
This gene is associated with the following 2 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
?Muscular dystrophy, congenital, Davignon-Chauveau type
617066AR
Spinal muscular atrophy with congenital bone fractures 1
616866AR

Diagnosed Cases

2Patients

In total, 2 patients were diagnosed with a variant in the TRIP4 gene.

Frequently observed phenotypes

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

Respiratory abnormality
 2 (100.0%)