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SLAIN1

SLAIN motif family member 1

HCNC Approved Symbol
SLAIN1 (HGNC:26387)
Genomic Coordinates
13:77,697,687 - 77,764,229 (13q22.3)
Synonyms
FLJ30046, C13orf32
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 21 patients* with variant(s) predicted to be damaging.*14 of the patients have been diagnosed with a variant in another gene.

SLAIN1 - Gene browser | 3billion