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GTF2H5

general transcription factor IIH subunit 5

HCNC Approved Symbol
GTF2H5 (HGNC:21157)
Genomic Coordinates
6:158,168,350 - 158,199,344 (6q25.3)
Synonyms
FLJ30544, bA120J8.2, TTD-A, TFB5, TFIIH, TTDA, C6orf175, TTD
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 GTF2H5 gene.

Frequently observed phenotypes

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

Congenital ichthyosis
 1 (100.0%)
Dry skin
 1 (100.0%)
GTF2H5 - Gene browser | 3billion