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SH3D21

SH3 domain containing 21

HCNC Approved Symbol
SH3D21 (HGNC:26236)
Genomic Coordinates
: - (1p34.3)
Synonyms
FLJ22938, C1orf113
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 2 patients* with variant(s) predicted to be damaging.*2 of the patients have been diagnosed with a variant in another gene.

SH3D21 - Gene browser | 3billion