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CMD1B cardiomyopathy, dilated 1B (autosomal dominant) [ Homo sapiens (human) ]

Gene ID: 1218, updated on 2-Oct-2019

Summary

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Gene symbol
CMD1B
Gene description
cardiomyopathy, dilated 1B (autosomal dominant)
Primary source
MIM:600884
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
FDC; CMPD1

Genomic context

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Location:
9q13-q22

Bibliography

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Related articles in PubMed

  1. Linkage of familial dilated cardiomyopathy to chromosome 9. Heart Muscle Disease Study Group. Krajinovic M, et al. Am J Hum Genet, 1995 Oct. PMID 7573045, Free PMC Article
  2. Merosin-deficient congenital muscular dystrophy with mental retardation and cerebellar cysts, unlinked to the LAMA2, FCMD, MEB and CMD1B loci, in three Tunisian patients. Triki C, et al. Neuromuscul Disord, 2003 Jan. PMID 12467726

GeneRIFs: Gene References Into Functions

What's a GeneRIF?
  1. Merosin-deficient congenital muscular dystrophy with mental retardation and cerebellar cysts, unlinked to the CMD1B locus in three Tunisian patients
    Title: Merosin-deficient congenital muscular dystrophy with mental retardation and cerebellar cysts, unlinked to the LAMA2, FCMD, MEB and CMD1B loci, in three Tunisian patients.
Submit: New GeneRIF Correction

Phenotypes

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cardiomyopathy, dilated 1B (autosomal dominant)

General gene information

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Property

  • phenotype only

Gene LinkOut

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Chemical Information
Molecular Biology Databases