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  3. SPNS2
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Deafness_Isolated

Gene: SPNS2

Amber List (moderate evidence)
SPNS2 (sphingolipid transporter 2)
EnsemblGeneIds (GRCh38): ENSG00000183018
EnsemblGeneIds (GRCh37): ENSG00000183018
OMIM: 612584, Gene2Phenotype
SPNS2 is in 3 panels

1 review

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

I don't know

Single family reported, mouse model shows progressive hearing loss.
Sources: Expert list
Created: 1 Jan 2020, 10:31 p.m.

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Phenotypes
Deafness, autosomal recessive 115, MIM# 618457

Publications

Created: 1 Jan 2020, 10:31 p.m.

Panel version: Imported from Deafness_IsolatedAndComplex panel version 0.163

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Expert list
  • Expert list
Phenotypes
  • Deafness, autosomal recessive 115, MIM# 618457
OMIM
612584
Clinvar variants
Variants in SPNS2
Penetrance
None
Publications
Panels with this gene

History Filter Activity

3 Oct 2020, Gel status: 2

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: spns2 has been classified as Amber List (Moderate Evidence).

21 Jul 2020, Gel status: 2

Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: SPNS2 was added gene: SPNS2 was added to DeafnessIsolated. Sources: Expert Review Amber,Expert list Mode of inheritance for gene: SPNS2 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: SPNS2 were set to 30973865; 25356849 Phenotypes for gene: SPNS2 were set to Deafness, autosomal recessive 115, MIM# 618457