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TIMM17B

translocase of inner mitochondrial membrane 17B

HCNC Approved Symbol
TIMM17B (HGNC:17310)
Genomic Coordinates
23:48,893,447 - 48,898,143 (Xp11.23)
Synonyms
DXS9822, JM3
Disease Associations
Currently, this gene is not associated with any human disease in OMIM.

Diagnosed Cases

There are no diagnosed cases at this time.
There are no patients* with variants predicted to be damaging.* None of the patients have been diagnosed with a variant in another gene.

TIMM17B - Gene browser | 3billion