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SSR4

signal sequence receptor subunit 4

HCNC Approved Symbol
SSR4 (HGNC:11326)
Genomic Coordinates
23:153,794,159 - 153,798,512 (Xq28)
Synonyms
TRAPD
Disease Associations
This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the SSR4 gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

No Results
SSR4 - Gene browser | 3billion