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GOLGA6B

golgin A6 family member B

HCNC Approved Symbol
GOLGA6B (HGNC:32205)
Genomic Coordinates
: - (15q24.1)
Synonyms
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.* None of the patients have been diagnosed with a variant in another gene.

GOLGA6B - Gene browser | 3billion