NEB Chromosome 2

Nebulin
2435 variants 2435 Health Risk

Upload your DNA to see your personal genotypes for variants in NEB.

What This Gene Does
This gene encodes nebulin, a giant protein component of the cytoskeletal matrix that coexists with the thick and thin filaments within the sarcomeres of skeletal muscle. In most vertebrates, nebulin accounts for 3 to 4% of the total myofibrillar protein. The encoded protein contains approximately 30-amino acid long modules that can be classified into 7 types and other repeated modules. Protein isoform sizes vary from 600 to 800 kD due to alternative splicing that is tissue-, species-,and developmental stage-specific. Of the 183 exons in the nebulin gene, at least 43 are alternatively spliced, although exons 143 and 144 are not found in the same transcript. Of the several thousand transcript variants predicted for nebulin, the RefSeq Project has decided to create three representative RefSeq records. Mutations in this gene are associated with recessive nemaline myopathy. [provided by RefSeq, Sep 2009]
Gene Info
Gene Group
Nebulin family
Locus Type
gene with protein product
Location
2q23.3
Ensembl
ENSG00000183091
Associated Conditions (28)
Nemaline myopathy 2
Inborn genetic diseases
Nemaline myopathy
Arthrogryposis multiplex congenita 6
NEB-related disorder
Actin accumulation myopathy
Distal myopathy
Nebulin-related early-onset distal myopathy
Clear cell carcinoma of kidney
Gastric cancer
Peripheral neuropathy
Limb-girdle muscular dystrophy
Congenital structural myopathy
Progressive proximal muscle weakness
Limb pain
Muscular dystrophy
See cases
Congenital myopathy
Melanoma
Muscle weakness
+8 more conditions
Key Variants
All Variants (2435)
RSID Category Clinical Significance Conditions
RS2552225895 Health Risk Pathogenic Nemaline myopathy 2, Nemaline myopathy 2
RS2552225936 Health Risk Pathogenic Nemaline myopathy 2, Nemaline myopathy 2
RS2552227141 Health Risk Pathogenic Nemaline myopathy 2, Nemaline myopathy 2
RS2552228093 Health Risk Pathogenic NEB-related disorder, NEB-related disorder
RS2552229054 Health Risk Pathogenic Nemaline myopathy 2, Nemaline myopathy 2
RS2552230087 Health Risk Pathogenic Nemaline myopathy 2, Nemaline myopathy 2
RS2552230097 Health Risk Pathogenic Nemaline myopathy 2, Nemaline myopathy 2
RS2552232032 Health Risk Pathogenic Nemaline myopathy, Nemaline myopathy
RS2552232037 Health Risk Pathogenic Nemaline myopathy 2, Nemaline myopathy 2
RS2552232690 Health Risk Pathogenic Nemaline myopathy 2, Nemaline myopathy 2
RS2552232745 Health Risk Pathogenic Nemaline myopathy 2, Nemaline myopathy 2
RS2552235365 Health Risk Pathogenic Nemaline myopathy 2, Nemaline myopathy 2
RS2552235371 Health Risk Pathogenic Nemaline myopathy 2, Nemaline myopathy 2
RS2552236321 Health Risk Pathogenic Nemaline myopathy 2, Nemaline myopathy 2
RS2552236675 Health Risk Pathogenic Nemaline myopathy 2, Nemaline myopathy 2
RS2552238326 Health Risk Pathogenic Nemaline myopathy 2, Nemaline myopathy 2
RS2552239780 Health Risk Pathogenic Nemaline myopathy 2, Nemaline myopathy 2
RS2552239840 Health Risk Pathogenic Nemaline myopathy 2, Nemaline myopathy 2
RS2552239864 Health Risk Pathogenic Nemaline myopathy 2, Nemaline myopathy 2
RS2552239867 Health Risk Pathogenic Nemaline myopathy 2, Nemaline myopathy 2
RS2552242957 Health Risk Pathogenic Arthrogryposis multiplex congenita 6, Arthrogryposis multiplex congenita 6
RS2552243919 Health Risk Pathogenic Nemaline myopathy 2, Nemaline myopathy 2
RS2552244056 Health Risk Pathogenic Inborn genetic diseases, Inborn genetic diseases
RS2552246923 Health Risk Pathogenic Nemaline myopathy, Nemaline myopathy
RS2552246978 Health Risk Pathogenic Nemaline myopathy 2, Nemaline myopathy 2
RS2552247669 Health Risk Pathogenic Nemaline myopathy 2, Nemaline myopathy 2
RS2552251128 Health Risk Pathogenic Nemaline myopathy 2, Nemaline myopathy 2
RS2552252226 Health Risk Pathogenic Nemaline myopathy 2, Nemaline myopathy 2
RS2552252600 Health Risk Pathogenic Nemaline myopathy 2, Nemaline myopathy 2
RS2552252653 Health Risk Pathogenic Nemaline myopathy 2, Nemaline myopathy 2
RS2552252667 Health Risk Pathogenic Nemaline myopathy 2, Nemaline myopathy 2
RS2552252715 Health Risk Pathogenic Arthrogryposis multiplex congenita 6, Arthrogryposis multiplex congenita 6
RS2552254223 Health Risk Pathogenic Nemaline myopathy 2, Nemaline myopathy 2
RS2552254257 Health Risk Pathogenic Nemaline myopathy 2, Nemaline myopathy 2
RS2552255606 Health Risk Pathogenic Nemaline myopathy, Nemaline myopathy
RS2552256930 Health Risk Pathogenic Nemaline myopathy 2, Nemaline myopathy 2
RS2552258164 Health Risk Pathogenic Nemaline myopathy 2, Nemaline myopathy 2
RS2552258220 Health Risk Pathogenic Nemaline myopathy 2, Nemaline myopathy 2
RS2552258297 Health Risk Pathogenic Nemaline myopathy 2, Nemaline myopathy 2
RS2552258309 Health Risk Pathogenic Nemaline myopathy 2, Nemaline myopathy 2
RS2552258957 Health Risk Pathogenic Nemaline myopathy 2, Nemaline myopathy 2
RS2552258964 Health Risk Pathogenic Nemaline myopathy 2, Nemaline myopathy 2
RS2552259329 Health Risk Pathogenic Nemaline myopathy 2, Nemaline myopathy 2
RS2552260630 Health Risk Pathogenic Nemaline myopathy 2, Nemaline myopathy 2
RS2552260663 Health Risk Pathogenic Nemaline myopathy 2, Nemaline myopathy 2
RS2552262530 Health Risk Pathogenic Nemaline myopathy 2, Nemaline myopathy 2
RS2552262536 Health Risk Pathogenic Nemaline myopathy 2, Nemaline myopathy 2
RS2552262537 Health Risk Pathogenic Nemaline myopathy 2, Nemaline myopathy 2
RS2552262538 Health Risk Pathogenic Nemaline myopathy 2, Nemaline myopathy 2
RS2552262719 Health Risk Pathogenic Nemaline myopathy 2, Nemaline myopathy 2
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