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SUPT20HL1

SUPT20H like 1

HCNC Approved Symbol
SUPT20HL1 (HGNC:30773)
Genomic Coordinates
: - (Xp22.11)
Synonyms
SPT20L, FAM48B1
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 23 patients* with variant(s) predicted to be damaging.*10 of the patients have been diagnosed with a variant in another gene.

SUPT20HL1 - Gene browser | 3billion