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FAM168A

family with sequence similarity 168 member A

HCNC Approved Symbol
FAM168A (HGNC:28999)
Genomic Coordinates
11:73,400,487 - 73,598,112 (11q13.4)
Synonyms
TCRP1, KIAA0280
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.*1 of the patient has been diagnosed with a variant in another gene.

FAM168A - Gene browser | 3billion