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TIMM22

translocase of inner mitochondrial membrane 22

HCNC Approved Symbol
TIMM22 (HGNC:17317)
Genomic Coordinates
17:997,129 - 1,003,671 (17p13)
Synonyms
TIM22, TEX4
Disease Associations
This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the TIMM22 gene.

Frequently observed phenotypes

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

No Results
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