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TIMM10B

translocase of inner mitochondrial membrane 10B

HCNC Approved Symbol
TIMM10B (HGNC:4022)
Genomic Coordinates
11:6,481,501 - 6,484,681 (11p15.4)
Synonyms
Tim9b, TIM10B, FXC1
Disease Associations
Currently, this gene is not associated with any human disease in OMIM.

Diagnosed Cases

There are no diagnosed cases at this time.
However, there is 1 patient* with variant(s) predicted to be damaging.*1 of the patient has been diagnosed with a variant in another gene.

TIMM10B - Gene browser | 3billion