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TRIM36

tripartite motif containing 36

HCNC Approved Symbol
TRIM36 (HGNC:16280)
Genomic Coordinates
5:115,124,772 - 115,180,294 (5q22.3)
Synonyms
RBCC728, RNF98, HAPRIN
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 TRIM36 gene.

Frequently observed phenotypes

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

No Results
TRIM36 - Gene browser | 3billion