Desmin

Alternative Names

  • DES
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OMIM Number

125660

NCBI Gene ID

1674

Uniprot ID

P17661

Length

8,358 bases

No. of Exons

9

No. of isoforms

1

Protein Name

Desmin

Molecular Mass

53536 Da

Amino Acid Count

470

Genomic Location

chr2:219,418,377-219,426,734

Gene Map Locus
2q35

Description

This gene encodes a muscle-specific class III intermediate filament. Homopolymers of this protein form a stable intracytoplasmic filamentous network connecting myofibrils to each other and to the plasma membrane. Mutations in this gene are associated with desmin-related myopathy, a familial cardiac and skeletal myopathy (CSM), and with distal myopathies. [From RefSeq]

Epidemiology in the Arab World

View Map
Variant NameCountryGenomic LocationClinvar Clinical SignificanceCTGA Clinical Significance Condition(s)HGVS ExpressionsdbSNPClinvar
NM_001927.4:c.1076_1084delSaudi ArabiaNC_000002.12:g.219421392_219421400delPathogenicLikely PathogenicMyopathy, Myofibrillar, Desmin-RelatedNG_008043.1:g.8016_8024del; NM_001927.4:c.1076_1084del; NP_001918.3:p.Glu359_Ser361del5840903766391
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