Gene table: search width pubmed_id = 19542096


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Disease phenotype
Item
in
this
table
Key
references
Gene symbol (chromosome)

protein
All allelic disease phenotypes - locus/disease symbols
Arthrogryposis multiplex congenita with nesprin-1 defect - (AR)
16.23
19542096
SYNE1 (6q25)
Spectrin repeat containing, nuclear envelope 1 (nesprin 1)
* Dilated cardiomyopathy related to nesprin-1
* Spinocerebellar ataxia, autosomal recessive 8 - SCAR8
* Emery-dreifuss muscular dystrophy 4 - EDMD4
* Arthrogryposis multiplex congenita with nesprin-1 defect - AMCM