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
RS368915047 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS368967111 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS369054525 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS369153778 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS369215974 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, See cases, NEB-related disorder
RS369224273 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy, Nemaline myopathy 2
RS369275207 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS369436489 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS369441230 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS369456343 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS369496057 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS369514998 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS369602540 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS369875205 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS369957704 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS370000978 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS370053963 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, NEB-related disorder
RS370108917 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy
RS370172690 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, NEB-related disorder, Nemaline myopathy 2
RS370189384 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Nemaline myopathy 2, Inborn genetic diseases
RS370206339 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS370663399 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS370695020 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS370738668 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS370764959 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS370810654 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS370873040 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS370924370 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS370976402 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS370994522 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS371015050 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS371105660 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS371109129 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS371194689 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS371265681 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, NEB-related disorder, Nemaline myopathy 2
RS371287755 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS371454282 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS371570995 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS371600800 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS371658494 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2, Nemaline myopathy 2
RS371675358 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS371681892 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS371689870 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS371704528 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS371771414 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
RS371816204 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS371909976 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Nemaline myopathy 2, Inborn genetic diseases
RS371938654 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS372037674 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Inborn genetic diseases, Nemaline myopathy 2
RS372042301 Health Risk Conflicting classifications of pathogenicity Nemaline myopathy 2, Nemaline myopathy 2
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