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Heritable Phenotypic Marker : Xlch X-linked cardiac hypertrophy

Primary Identifier	MGI:3797603	Organism	mouse, laboratory
Chromosome	X	Mgi Type	heritable phenotypic marker

description

FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0)

Used to study X-linked dilated cardiomyopathy.
PHENOTYPE: Heterozygotes for this ENU-induced mutation exhibit cardiac hypertrophy and partial lethality at birth. [provided by MGI curators]

synonyms:
Xlch,
X-linked cardiac hypertrophy,
Family 78,
Hlb545

Features --> Cross References

Genome

Sequence Feature Displayer

JG Browse Displayer

0 Involved In Mutations

0 Transgenic Expressors

Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

Canonical gene --> Strain-specific IDs, biotypes, and locations

Canonical gene --> Transcripts in specific strains.

Features --> Overlapping features

Proteins

Gene --> Proteins

Function

Mouse features --> Functions (GO terms)

Homology

Genes --> Homologs

Interactions

Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

Mouse features --> Publications

Other

0 Driver For

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