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SUPT20HL2

SUPT20H like 2

HCNC Approved Symbol
SUPT20HL2 (HGNC:31797)
Genomic Coordinates
: - (Xp22.11)
Synonyms
FAM48B2
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 are 6 patients* with variant(s) predicted to be damaging.*3 of the patients have been diagnosed with a variant in another gene.

SUPT20HL2 - Gene browser | 3billion