The association between RNF135 (Ring Finger Protein 135) and Chromosome 17q11.2 Deletion Syndrome, 1.4-Mb is well established and manually curated, with its 2 contributing sources — 1 of them expert-curated — recording a causative germline mutation.
Sources2
Clinical variants5
Symptoms92
Compounds0
Trials0
Publications1
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.