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Hearing loss


Red List (low evidence)

NEUROD1 (neuronal differentiation 1)
EnsemblGeneIds (GRCh38): ENSG00000162992
EnsemblGeneIds (GRCh37): ENSG00000162992
OMIM: 601724, Gene2Phenotype
NEUROD1 is in 7 panels

1 review

Jun Shen (Harvard Medical School)

Red List (low evidence)

Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown

#125853:{Diabetes mellitus, noninsulin-dependent}[Noninsulin-dependent diabetes mellitus; Late onset; Insulin resistance; Decreased glucose disposal]; #606394:Maturity-onset diabetes of the young 6[<omim version=1.0><clinicalSynopsisList>]


History Filter Activity

24 Jun 2015, Gel status: 0

Added New Source

Ellen McDonagh (Genomics England Curator)

NEUROD1 was added to Congenital hearing impairment (Profound/Severe)panel. Sources: Expert