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
RS183088493 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS183333679 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS183354017 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS183667452 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS183764569 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS184319249 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS184516994 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, NEB-related disorder, Clear cell carcinoma of kidney
RS184723737 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS185433570 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS185441677 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS185496567 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS185574478 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS185674525 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, NEB-related disorder, Nemaline myopathy 2
RS185727779 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS185999504 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Arthrogryposis multiplex congenita 6, Nemaline myopathy 2
RS186233985 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS186244044 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS186686151 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS187977960 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, NEB-related disorder
RS189232206 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS189541265 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS189553632 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, NEB-related disorder
RS189609282 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, NEB-related disorder, Nemaline myopathy 2
RS189617624 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS189623595 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, NEB-related disorder, Nemaline myopathy 2
RS190132249 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS190336010 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS190605644 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2, Inborn genetic diseases
RS191722579 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS192402741 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, NEB-related disorder, Nemaline myopathy 2
RS193224180 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, NEB-related disorder
RS199511221 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS199551865 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS199584268 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Arthrogryposis multiplex congenita 6, Nemaline myopathy 2
RS199594449 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS199662534 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS199694315 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS199695976 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS199700878 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, NEB-related disorder
RS199710125 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Arthrogryposis multiplex congenita 6, Nemaline myopathy 2
RS199722285 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS199730497 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, NEB-related disorder, Nemaline myopathy 2
RS199756204 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS199789085 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, NEB-related disorder, Nemaline myopathy 2
RS199804593 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Gastric cancer, Nemaline myopathy 2
RS199847072 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, NEB-related disorder
RS199862790 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, NEB-related disorder
RS199875722 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS199890298 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, NEB-related disorder
RS199894970 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
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