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PNISR

PNN interacting serine and arginine rich protein

HCNC Approved Symbol
PNISR (HGNC:21222)
Genomic Coordinates
6:99,398,050 - 99,425,308 (6q16.2)
Synonyms
FLJ14752, bA98I9.2, DKFZp564B0769, SRrp130, C6orf111, SFRS18
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 11 patients* with variant(s) predicted to be damaging.*4 of the patients have been diagnosed with a variant in another gene.

PNISR - Gene browser | 3billion