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SLFN13

schlafen family member 13

HCNC Approved Symbol
SLFN13 (HGNC:26481)
Genomic Coordinates
17:35,435,096 - 35,449,766 (17q12)
Synonyms
FLJ31952
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.

SLFN13 - Gene browser | 3billion