NEB Chromosome 2

Nebulin
2435 variants 2435 Health Risk

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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
RS533233215 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Arthrogryposis multiplex congenita 6, Nemaline myopathy 2
RS533393007 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS534443920 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS534519331 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Arthrogryposis multiplex congenita 6
RS534531948 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS534646949 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS535926481 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS536677256 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS536934629 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS537769519 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS538068134 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS539800267 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS539856643 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS540542570 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, NEB-related disorder, Nemaline myopathy 2
RS541641039 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS541672313 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS542092706 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS542149432 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS542706227 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS543100735 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS543961404 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS544200886 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS544334101 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS545889830 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS546250852 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS546869744 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Arthrogryposis multiplex congenita 6
RS547109690 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS547852316 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS549227905 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS549794342 Health Risk Conflicting classifications of pathogenicity Limb pain, Progressive proximal muscle weakness, Muscular dystrophy
RS550191566 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS550296441 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS550715282 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS551520922 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, NEB-related disorder, Nemaline myopathy 2
RS551649582 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS553079055 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS553375465 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS554366790 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS554984749 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nebulin-related early-onset distal myopathy, Nemaline myopathy 2
RS556492694 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS556624010 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS556930902 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Arthrogryposis multiplex congenita 6, Nemaline myopathy 2
RS557688789 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS557950249 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS558019875 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS558345996 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS559846137 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS560109089 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS561736266 Health Risk Conflicting classifications of pathogenicity
RS561904743 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
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