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Heritable Phenotypic Marker : olt oligotriche

Primary Identifier	MGI:97433	Organism	mouse, laboratory
Chromosome	9	Mgi Type	heritable phenotypic marker

description

PHENOTYPE: Mice homozygous for a spontaneous mutation exhibit abnormal hair shaft and hair follicle morphology, abnormal hair cycle catagen phase, regional alopecia, and male sterility associated with defects in sperm tail formation during spermiogenesis. [provided by MGI curators]

synonyms:
oligotriche,
MGD-MRK-13030,
olt,
Del(9)olt1Pas,
Del(9Ctdspl-Slc22a14)1Pas

earliestPublication:
Chubb C (1992) Oligotriche and quaking gene mutations. Phenotypic effects on mouse spermatogenesis and testicular steroidogenesis. J Androl 13(4):312-7

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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