Genes in panel
STRs in panel
Prev Next
Regions in panel
Prev Next

Hearing loss

Gene: SCRIB

Red List (low evidence)

SCRIB (scribbled planar cell polarity protein)
EnsemblGeneIds (GRCh38): ENSG00000180900
EnsemblGeneIds (GRCh37): ENSG00000180900
OMIM: 607733, Gene2Phenotype
SCRIB is in 3 panels

1 review

Jun Shen (Harvard Medical School)

Red List (low evidence)

SCRIB is not associated with a phenotype entry in OMIM.
Created: 9 Feb 2016, 10:08 a.m.
SCRIB is not associated with a phenotype entry in OMIM.
Created: 7 Feb 2016, 3:45 p.m.

Publications

Details

Sources
  • Expert
OMIM
607733
Clinvar variants
Variants in SCRIB
Penetrance
Complete
Panels with this gene

History Filter Activity

24 Jun 2015, Gel status: 0

Added New Source

Ellen McDonagh (Genomics England Curator)

SCRIB was added to Congenital hearing impairment (Profound/Severe)panel. Sources: Expert