Redic1 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Redic1
regulator of DNA class I crossover intermediates 1
MGI:3613655

24 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Redic1^em2Qsh/Redic1^em2Qsh C57BL/6-Redic1^em2Qsh	abnormal chromosomal synapsis	J:383089
	abnormal meiosis	J:383089
	abnormal meiotic spindle morphology	J:383089
	abnormal oocyte morphology	J:383089
	abnormal seminiferous tubule morphology	J:383089
	abnormal spermatocyte morphology	J:383089
	abnormal X-Y chromosome synapsis during male meiosis	J:383089
	absent mature ovarian follicles	J:383089
	absent primary ovarian follicles	J:383089
	absent primordial ovarian follicles	J:383089
	absent tertiary ovarian follicles	J:383089
	arrest of male meiosis	J:383089
	arrest of spermatogenesis	J:383089
	azoospermia	J:383089
	decreased primary ovarian follicle number	J:383089
	decreased primordial ovarian follicle number	J:383089
	decreased secondary ovarian follicle number	J:383089
	decreased testis weight	J:383089
	female infertility	J:383089
	impaired double-strand DNA break repair	J:383089
	impaired ovarian folliculogenesis	J:383089
	infertility	J:383089
	male infertility	J:383089
	small testis	J:383089

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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