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Hearing loss

Gene: SLC4A7

Red List (low evidence)

SLC4A7 (solute carrier family 4 member 7)
EnsemblGeneIds (GRCh38): ENSG00000033867
EnsemblGeneIds (GRCh37): ENSG00000033867
OMIM: 603353, Gene2Phenotype
SLC4A7 is in 1 panel

1 review

Jun Shen (Harvard Medical School)

Red List (low evidence)

SLC4A7 is not associated with a phenotype entry in OMIM.
Created: 9 Feb 2016, 10:08 a.m.
SLC4A7 is not associated with a phenotype entry in OMIM.
Created: 7 Feb 2016, 3:46 p.m.

Publications

Details

Sources
  • Expert
OMIM
603353
Clinvar variants
Variants in SLC4A7
Penetrance
Complete
Panels with this gene

History Filter Activity

24 Jun 2015, Gel status: 0

Added New Source

Ellen McDonagh (Genomics England Curator)

SLC4A7 was added to Congenital hearing impairment (Profound/Severe)panel. Sources: Expert