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SSR2

signal sequence receptor subunit 2

HCNC Approved Symbol
SSR2 (HGNC:11324)
Genomic Coordinates
1:156,009,048 - 156,020,951 (1q22)
Synonyms
TLAP, TRAPB
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.