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Heritable Phenotypic Marker : mei2-7 meiosis defective 2.7
Primary Identifier  MGI:3050558 Organism  mouse, laboratory
Chromosome  7 Mgi Type  heritable phenotypic marker
description  PHENOTYPE: Males homozygous for this EMS-induced mutation are sterile with most spermatocytes undergoing meiotic arrest around the pachytene stage. Some postmeiotic round spermatids can be seen but no later stages of spermatogenesis are observed. Testis size variesdepending on the genetic background. [provided by MGI curators]
  • synonyms:
  • meiosis defective 2.7,
  • mei2-7
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Genome

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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

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