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RCM2 cardiomyopathy, familial restrictive, 2 [ Homo sapiens (human) ]

Gene ID: 619468, updated on 31-Aug-2024

Summary

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Official Symbol
RCM2provided by HGNC
Official Full Name
cardiomyopathy, familial restrictive, 2provided by HGNC
Primary source
MIM:609578
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo

Genomic context

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Location:
10q23.3

Bibliography

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Related articles in PubMed

  1. Genetic linkage of a novel autosomal dominant restrictive cardiomyopathy locus. Zhang J, et al. J Med Genet, 2005 Aug. PMID 16061566, Free PMC Article

GeneRIFs: Gene References Into Functions

Phenotypes

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Associated conditions

Description Tests
cardiomyopathy, familial restrictive, 2
OMIM: 609578GeneReviews: Not available

General gene information

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Markers

Property

  • phenotype only

Gene LinkOut

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