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CMD1F cardiomyopathy, dilated 1F (autosomal dominant) [ Homo sapiens (human) ]

Gene ID: 1222, discontinued on 25-Jul-2017

Summary

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Official Symbol
CMD1Fprovided by HGNC
Official Full Name
cardiomyopathy, dilated 1F (autosomal dominant)provided by HGNC
Primary source
HGNC:HGNC:2106
See related
MIM:602067
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
CDCD3; LGMD1D; LGMD1E
Annotation information
Note: We recognize that OMIM uses LGMD1D to refer to the locus on chromosome 6. There are many citations, however, including PubMed 8533766, 15316618, 20682716, and 21376592 which define LGMD1D as the locus on chromosome 7. We are retaining the usage of the HUGO Gene Nomenclature Committee (HGNC). [13 Feb 2013]

Genomic context

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Location:
6q23

Bibliography

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GeneRIFs: Gene References Into Functions

Phenotypes

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Associated conditions

Description Tests
cardiomyopathy, dilated 1F (autosomal dominant)
GeneReviews: Not available

General gene information

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Property

  • phenotype only

Gene LinkOut

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