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
RS144168709 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS144180493 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS144303545 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, NEB-related disorder, Nemaline myopathy 2
RS144539316 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, NEB-related disorder
RS144595998 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS144673752 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS1449487575 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS1452109473 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS1460365350 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Arthrogryposis multiplex congenita 6, Nemaline myopathy
RS1465332264 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS146616621 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, NEB-related disorder, Inborn genetic diseases
RS146637177 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS1466496551 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS1468240932 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS147159176 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, NEB-related disorder, Nemaline myopathy 2
RS1472489170 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS147476634 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS1475846023 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS147872436 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS148455519 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS1487589344 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Arthrogryposis multiplex congenita 6, Inborn genetic diseases
RS148794372 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS149384863 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS149430473 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS149471462 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Arthrogryposis multiplex congenita 6, Nemaline myopathy 2
RS149596493 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS149606244 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS149881695 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS150496369 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS150874422 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Arthrogryposis multiplex congenita 6, NEB-related disorder
RS150961139 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS151338614 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS1553520266 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy, Nemaline myopathy 2
RS1553715636 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Arthrogryposis multiplex congenita 6, Nemaline myopathy
RS1553877493 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS1553877949 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS1553966356 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS1558825869 Health Risk Conflicting classifications of pathogenicity
RS1575897069 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS16830171 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS180779260 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Nemaline myopathy 2, Inborn genetic diseases
RS181244403 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS181642642 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS181826071 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS182207224 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS182252292 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS182325166 Health Risk Conflicting classifications of pathogenicity Nebulin-related early-onset distal myopathy, Nemaline myopathy 2, Nebulin-related early-onset distal myopathy
RS182699929 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS182847302 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS182866658 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, NEB-related disorder, Nemaline myopathy 2
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