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GOLGA7B

golgin A7 family member B

HCNC Approved Symbol
GOLGA7B (HGNC:31668)
Genomic Coordinates
10:97,849,843 - 97,871,578 (10q24.2)
Synonyms
bA459F3.4, bA451M19.3, C10orf133, C10orf132
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.

GOLGA7B - Gene browser | 3billion