SYNE4 Chromosome 19

Spectrin repeat containing nuclear envelope family member 4
52 variants 52 Health Risk

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What This Gene Does
This gene is a member of the nesprin family of genes, that encode KASH (Klarsicht, Anc-1, Syne Homology) domain-containing proteins. In addition to the KASH domain, this protein also contains a coiled-coil and leucine zipper region, a spectrin repeat, and a kinesin-1 binding region. This protein localizes to the outer nuclear membrane, and is part of the linker of nucleoskeleton and cytoskeleton (LINC) complex in the nuclear envelope. LINC complexes are formed by SUN (Sad1, UNC-84)-KASH pairs, and are thought to mechanically couple nuclear components to the cytoskeleton. Mutations in this gene have been associated with progressive high-frequency hearing loss. The absence of this protein in mice also caused hearing loss, and changes in hair cell morphology in the ears. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Aug 2015]
Gene Info
Gene Group
"Spectrin repeat containing nuclear envelope family|KASH domain containing"
Locus Type
gene with protein product
Location
19q13.12
Ensembl
ENSG00000181392
Associated Conditions (7)
SYNE4-related disorder
Familial cancer of breast
Nonsyndromic genetic hearing loss
Autosomal recessive nonsyndromic hearing loss 76
Monogenic hearing loss
Ovarian serous cystadenocarcinoma
Rare genetic deafness
Key Variants
All Variants (52)
RSID Category Clinical Significance Conditions
RS772404105 Health Risk Pathogenic/Likely pathogenic Autosomal recessive nonsyndromic hearing loss 76, Autosomal recessive nonsyndromic hearing loss 76
RS776772746 Health Risk Pathogenic/Likely pathogenic Autosomal recessive nonsyndromic hearing loss 76, Autosomal recessive nonsyndromic hearing loss 76
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