Nebulin

Alternative Names

  • NEB

Associated Diseases

Nemaline Myopathy 2
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OMIM Number

161650

NCBI Gene ID

4703

Uniprot ID

P20929

Length

249,138 bases

No. of Exons

183

No. of isoforms

4

Protein Name

Nebulin

Molecular Mass

986665 Da

Amino Acid Count

8525

Genomic Location

chr2:151,485,339-151,734,476

Gene Map Locus
2q23.3

Description

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. [From RefSeq]

Epidemiology in the Arab World

View Map
Variant NameCountryGenomic LocationClinvar Clinical SignificanceCTGA Clinical Significance Condition(s)HGVS ExpressionsdbSNPClinvar
NM_001164508.2:c.11806-1G>ASaudi ArabiaNC_000002.12:g.151610867C>TLikely Pathogenic, PathogenicLikely PathogenicNemaline Myopathy 2NG_009382.2:g.128621G>A; NM_001164508.2:c.11806-1G>A; NP_001157980.2:p.?886041851280692
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