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SLFN12

schlafen family member 12

HCNC Approved Symbol
SLFN12 (HGNC:25500)
Genomic Coordinates
17:35,410,922 - 35,433,174 (17q12)
Synonyms
FLJ10260
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 4 patients* with variant(s) predicted to be damaging.*1 of the patient has been diagnosed with a variant in another gene.

SLFN12 - Gene browser | 3billion