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INTS13

integrator complex subunit 13

HCNC Approved Symbol
INTS13 (HGNC:20174)
Genomic Coordinates
12:26,905,181 - 26,938,332 (12p11.23)
Synonyms
FLJ10637, NET48, Mat89Bb, SPATA30, C12orf11, ASUN
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 3 patients* with variant(s) predicted to be damaging.* None of the patients have been diagnosed with a variant in another gene.