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
RS764278567 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS764377335 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS764417105 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS764457781 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS764524918 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS764538619 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS764674361 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Arthrogryposis multiplex congenita 6, Nemaline myopathy 2
RS764730223 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS764757576 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS764901671 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS765006379 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS765189771 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS765248215 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS765273968 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS765363585 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS765394821 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS765478068 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS765569689 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS765644258 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS765789028 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Nemaline myopathy 2, Inborn genetic diseases
RS765806782 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS765921628 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS765940770 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS766019243 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS766072117 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS766175179 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS766254214 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS766357828 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS766467431 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Nemaline myopathy 2, Inborn genetic diseases
RS766827189 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS766943894 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS767095639 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS767207985 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS767302772 Health Risk Conflicting classifications of pathogenicity Arthrogryposis multiplex congenita 6, Nemaline myopathy 2, Nemaline myopathy
RS767328072 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS767425744 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS767433330 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS767461697 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS767493706 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Arthrogryposis multiplex congenita 6, Inborn genetic diseases
RS767584361 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS767593840 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS767772838 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy, Nemaline myopathy 2
RS767858255 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS767873861 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS767886794 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS767969927 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS768012126 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS768363495 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS768390701 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS768693028 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
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