The association between SPECC1L (Sperm Antigen With Calponin Homology And Coiled-Coil Domains 1 Like) and Teebi Hypertelorism Syndrome 1 is well established and manually curated, with its 5 contributing sources — 4 of them expert-curated — recording a known molecular basis, likely-pathogenic variants, and a causative germline mutation.
Sources5
Clinical variants44
Symptoms87
Compounds0
Trials0
Publications6
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.