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Heritable Phenotypic Marker : repro48 reproductive mutation 48, JAX Reproductive Mutagenesis Program

Primary Identifier	MGI:3692896	Organism	mouse, laboratory
Chromosome	UN	Mgi Type	heritable phenotypic marker

description

PHENOTYPE: Homozygotes for this ENU-induced mutation exhibit male reproductive abnormalities including infertility, abnormal spermiogenesis, oligozoospermia, and low seminal vesicle weight. [provided by MGI curators]

synonyms:
G1-598-5,
repro48,
reproductive mutation 48, JAX Reproductive Mutagenesis Program

earliestPublication:
JAX Reproductive Mutagenesis Program (2004) Heritable mouse mutants from The Jackson Laboratory Reproductive Genomics Mutagenesis Program. MGI Direct Data Submission

Features --> Cross References

Genome

Sequence Feature Displayer

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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

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