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
RS2153619687 Health Risk Pathogenic Emery-Dreifuss muscular dystrophy 4, autosomal dominant, Autosomal recessive ataxia
RS2153628887 Health Risk Pathogenic
RS2153709458 Health Risk Pathogenic Emery-Dreifuss muscular dystrophy 4, autosomal dominant, Autosomal recessive ataxia
RS2153732048 Health Risk Pathogenic Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
RS2153783491 Health Risk Pathogenic Autosomal recessive ataxia, Beauce type, Autosomal recessive ataxia
RS2153809530 Health Risk Pathogenic Emery-Dreifuss muscular dystrophy 4, autosomal dominant, Autosomal recessive ataxia
RS2153969039 Health Risk Pathogenic
RS2153970781 Health Risk Pathogenic Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
RS2153971833 Health Risk Pathogenic
RS2154018964 Health Risk Pathogenic
RS2154044401 Health Risk Pathogenic
RS2154115529 Health Risk Pathogenic Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
RS2154133792 Health Risk Pathogenic Autosomal recessive ataxia, Beauce type, Autosomal recessive ataxia
RS2154147676 Health Risk Pathogenic Autosomal recessive ataxia, Beauce type, Autosomal recessive ataxia
RS2154151091 Health Risk Pathogenic Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
RS2154157186 Health Risk Pathogenic Autosomal recessive ataxia, Beauce type, Autosomal recessive ataxia
RS2154170060 Health Risk Pathogenic Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
RS2154182475 Health Risk Pathogenic
RS2154182611 Health Risk Pathogenic Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
RS2154239396 Health Risk Pathogenic
RS2154254291 Health Risk Pathogenic Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
RS2154331501 Health Risk Pathogenic Spastic ataxia, Emery-Dreifuss muscular dystrophy 4, autosomal dominant
RS2154353746 Health Risk Pathogenic Emery-Dreifuss muscular dystrophy 4, autosomal dominant, Autosomal recessive ataxia
RS2484737456 Health Risk Pathogenic Autosomal recessive ataxia, Beauce type, Autosomal recessive ataxia
RS2485325706 Health Risk Pathogenic Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
RS2485345197 Health Risk Pathogenic Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
RS2485626958 Health Risk Pathogenic Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
RS2485959310 Health Risk Pathogenic
RS2488638913 Health Risk Pathogenic Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
RS2490994680 Health Risk Pathogenic Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
RS2497999874 Health Risk Pathogenic SYNE1-related disorder, SYNE1-related disorder
RS2499274206 Health Risk Pathogenic Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
RS2500815673 Health Risk Pathogenic Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
RS2501656603 Health Risk Pathogenic Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
RS2505832456 Health Risk Pathogenic Emery-Dreifuss muscular dystrophy 4, autosomal dominant, Autosomal recessive ataxia
RS2549722965 Health Risk Pathogenic Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
RS2549805387 Health Risk Pathogenic Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
RS2550008477 Health Risk Pathogenic Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
RS2550010488 Health Risk Pathogenic Emery-Dreifuss muscular dystrophy 4, autosomal dominant, Autosomal recessive ataxia
RS2550229446 Health Risk Pathogenic Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
RS2550289323 Health Risk Pathogenic
RS2551032977 Health Risk Pathogenic Arthrogryposis multiplex congenita 3, myogenic type, Arthrogryposis multiplex congenita 3
RS2551496109 Health Risk Pathogenic
RS2551505402 Health Risk Pathogenic Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
RS2551617809 Health Risk Pathogenic Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
RS2551694835 Health Risk Pathogenic Emery-Dreifuss muscular dystrophy 4, autosomal dominant, Autosomal recessive ataxia
RS2551698321 Health Risk Pathogenic Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
RS2551881997 Health Risk Pathogenic Emery-Dreifuss muscular dystrophy 4, autosomal dominant, Autosomal recessive ataxia
RS2551882028 Health Risk Pathogenic Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
RS2552072090 Health Risk Pathogenic Autosomal recessive ataxia, Beauce type, Emery-Dreifuss muscular dystrophy 4
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