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FAM89B

family with sequence similarity 89 member B

HCNC Approved Symbol
FAM89B (HGNC:16708)
Genomic Coordinates
11:65,572,538 - 65,574,190 (11q13.1)
Synonyms
MTVR1, LRAP25
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.

FAM89B - Gene browser | 3billion