SYNE1 Chromosome 6

Spectrin repeat containing nuclear envelope protein 1
882 variants 882 Health Risk

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What This Gene Does
This gene encodes a spectrin repeat containing protein expressed in skeletal and smooth muscle, and peripheral blood lymphocytes, that localizes to the nuclear membrane. Mutations in this gene have been associated with autosomal recessive spinocerebellar ataxia 8, also referred to as autosomal recessive cerebellar ataxia type 1 or recessive ataxia of Beauce. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
"Spectrin repeat containing nuclear envelope family|KASH domain containing"
Locus Type
gene with protein product
Location
6q25.2
Ensembl
ENSG00000131018
Associated Conditions (41)
Autosomal recessive ataxia
Beauce type
Emery-Dreifuss muscular dystrophy 4
autosomal dominant
Abnormal brain morphology
Inborn genetic diseases
SYNE1-related disorder
Hereditary ataxia
Arthrogryposis syndrome
Intellectual disability
Arthrogryposis multiplex congenita 3
myogenic type
Thyroid cancer
nonmedullary
1
Limb-girdle muscular dystrophy
Spastic ataxia
Clear cell carcinoma of kidney
Hepatocellular carcinoma
Familial cancer of breast
+21 more conditions
Key Variants
RS1014746277
Conflicting classifications of pathogenicity
Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
Health Risk
RS1020832262
Conflicting classifications of pathogenicity
Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
Health Risk
RS1057521423
Conflicting classifications of pathogenicity
Emery-Dreifuss muscular dystrophy 4, autosomal dominant, Autosomal recessive ataxia
Health Risk
RS1057522688
Conflicting classifications of pathogenicity
Health Risk
RS1057523855
Conflicting classifications of pathogenicity
Health Risk
RS1060499769
Conflicting classifications of pathogenicity
Abnormal brain morphology, Emery-Dreifuss muscular dystrophy 4, autosomal dominant
Health Risk
RS111367233
Conflicting classifications of pathogenicity
Emery-Dreifuss muscular dystrophy 4, autosomal dominant, Autosomal recessive ataxia
Health Risk
RS111511993
Conflicting classifications of pathogenicity
Emery-Dreifuss muscular dystrophy 4, autosomal dominant, Autosomal recessive ataxia
Health Risk
RS112744561
Conflicting classifications of pathogenicity
Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
Health Risk
RS113163375
Conflicting classifications of pathogenicity
Emery-Dreifuss muscular dystrophy 4, autosomal dominant, Autosomal recessive ataxia
Health Risk
RS113962905
Conflicting classifications of pathogenicity
Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
Health Risk
RS114858512
Conflicting classifications of pathogenicity
Emery-Dreifuss muscular dystrophy 4, autosomal dominant, Autosomal recessive ataxia
Health Risk
All Variants (882)
RSID Category Clinical Significance Conditions
RS1014746277 Health Risk Conflicting classifications of pathogenicity Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
RS1020832262 Health Risk Conflicting classifications of pathogenicity Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
RS1057521423 Health Risk Conflicting classifications of pathogenicity Emery-Dreifuss muscular dystrophy 4, autosomal dominant, Autosomal recessive ataxia
RS1057522688 Health Risk Conflicting classifications of pathogenicity
RS1057523855 Health Risk Conflicting classifications of pathogenicity
RS1060499769 Health Risk Conflicting classifications of pathogenicity Abnormal brain morphology, Emery-Dreifuss muscular dystrophy 4, autosomal dominant
RS111367233 Health Risk Conflicting classifications of pathogenicity Emery-Dreifuss muscular dystrophy 4, autosomal dominant, Autosomal recessive ataxia
RS111511993 Health Risk Conflicting classifications of pathogenicity Emery-Dreifuss muscular dystrophy 4, autosomal dominant, Autosomal recessive ataxia
RS112744561 Health Risk Conflicting classifications of pathogenicity Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
RS113163375 Health Risk Conflicting classifications of pathogenicity Emery-Dreifuss muscular dystrophy 4, autosomal dominant, Autosomal recessive ataxia
RS113962905 Health Risk Conflicting classifications of pathogenicity Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
RS114858512 Health Risk Conflicting classifications of pathogenicity Emery-Dreifuss muscular dystrophy 4, autosomal dominant, Autosomal recessive ataxia
RS115534729 Health Risk Conflicting classifications of pathogenicity Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
RS115535983 Health Risk Conflicting classifications of pathogenicity Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
RS116721144 Health Risk Conflicting classifications of pathogenicity Emery-Dreifuss muscular dystrophy 4, autosomal dominant, Autosomal recessive ataxia
RS117084693 Health Risk Conflicting classifications of pathogenicity Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
RS117346210 Health Risk Conflicting classifications of pathogenicity Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
RS117360770 Health Risk Conflicting classifications of pathogenicity Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
RS117461489 Health Risk Conflicting classifications of pathogenicity Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
RS117480635 Health Risk Conflicting classifications of pathogenicity Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
RS118022241 Health Risk Conflicting classifications of pathogenicity Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
RS118187988 Health Risk Conflicting classifications of pathogenicity Emery-Dreifuss muscular dystrophy 4, autosomal dominant, Autosomal recessive ataxia
RS119103248 Health Risk Conflicting classifications of pathogenicity Emery-Dreifuss muscular dystrophy 4, autosomal dominant, Autosomal recessive ataxia
RS1193871694 Health Risk Conflicting classifications of pathogenicity Emery-Dreifuss muscular dystrophy 4, autosomal dominant, Autosomal recessive ataxia
RS1209321050 Health Risk Conflicting classifications of pathogenicity Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
RS1235198872 Health Risk Conflicting classifications of pathogenicity Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
RS1265561583 Health Risk Conflicting classifications of pathogenicity Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
RS1337751426 Health Risk Conflicting classifications of pathogenicity Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
RS1347407918 Health Risk Conflicting classifications of pathogenicity Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
RS137919524 Health Risk Conflicting classifications of pathogenicity Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
RS138004884 Health Risk Conflicting classifications of pathogenicity Emery-Dreifuss muscular dystrophy 4, autosomal dominant, Autosomal recessive ataxia
RS138039375 Health Risk Conflicting classifications of pathogenicity Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
RS138173087 Health Risk Conflicting classifications of pathogenicity Emery-Dreifuss muscular dystrophy 4, autosomal dominant, Autosomal recessive ataxia
RS138196409 Health Risk Conflicting classifications of pathogenicity Emery-Dreifuss muscular dystrophy 4, autosomal dominant, Autosomal recessive ataxia
RS138277154 Health Risk Conflicting classifications of pathogenicity Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
RS138307449 Health Risk Conflicting classifications of pathogenicity Emery-Dreifuss muscular dystrophy 4, autosomal dominant, Autosomal recessive ataxia
RS138368397 Health Risk Conflicting classifications of pathogenicity Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
RS138407813 Health Risk Conflicting classifications of pathogenicity Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
RS138509817 Health Risk Conflicting classifications of pathogenicity Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
RS138617999 Health Risk Conflicting classifications of pathogenicity Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
RS138650597 Health Risk Conflicting classifications of pathogenicity Emery-Dreifuss muscular dystrophy 4, autosomal dominant, Autosomal recessive ataxia
RS138745849 Health Risk Conflicting classifications of pathogenicity Emery-Dreifuss muscular dystrophy 4, autosomal dominant, Autosomal recessive ataxia
RS138882800 Health Risk Conflicting classifications of pathogenicity Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
RS139070088 Health Risk Conflicting classifications of pathogenicity Emery-Dreifuss muscular dystrophy 4, autosomal dominant, Autosomal recessive ataxia
RS139075013 Health Risk Conflicting classifications of pathogenicity Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
RS139078338 Health Risk Conflicting classifications of pathogenicity Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
RS139079964 Health Risk Conflicting classifications of pathogenicity Emery-Dreifuss muscular dystrophy 4, autosomal dominant, Autosomal recessive ataxia
RS139089832 Health Risk Conflicting classifications of pathogenicity Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
RS139139296 Health Risk Conflicting classifications of pathogenicity Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
RS139170018 Health Risk Conflicting classifications of pathogenicity Emery-Dreifuss muscular dystrophy 4, autosomal dominant, Autosomal recessive ataxia
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