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FAM168B

family with sequence similarity 168 member B

HCNC Approved Symbol
FAM168B (HGNC:27016)
Genomic Coordinates
2:131,047,876 - 131,093,460 (2q21.1)
Synonyms
KIAA0280L, MANI
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.

FAM168B - Gene browser | 3billion