Rad21l Phenotype Annotations - Multigenic Genotypes

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Rad21l
RAD21-like (S. pombe)
MGI:3652039

21 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Prdm9^tm1Ymat/Prdm9^tm1Ymat Rad21l^{tm1b(KOMP)Wtsi}/Rad21l^{tm1b(KOMP)Wtsi} B6.Cg-Prdm9^tm1Ymat Rad21l^{tm1b(KOMP)Wtsi}	normal cellular phenotype	J:280261
Rad21l^tm1Amp/Rad21l^tm1Amp B6.Cg-Rad21l^tm1Amp	abnormal male meiosis	J:205574
Rad21l^tm1Amp/Rad21l^tm1Amp involves: 129S6/SvEvTac * C57BL/6NCr	abnormal double-strand DNA break repair	J:176168
	abnormal female meiosis	J:176168
	abnormal male germ cell apoptosis	J:176168
	abnormal male meiosis	J:176168
	abnormal synaptonemal complex	J:176168
	abnormal telomere morphology	J:176168
	absent primordial ovarian follicles	J:176168
	arrest of male meiosis	J:176168
	arrest of spermatogenesis	J:176168
	azoospermia	J:176168
	decreased litter size	J:176168
	decreased mature ovarian follicle number	J:176168
	decreased oocyte number	J:176168
	male infertility	J:176168
	ovary atrophy	J:176168
	ovary fibrosis	J:176168
	reduced female fertility	J:176168
	small testis	J:176168
Rad21l^{tm1b(KOMP)Wtsi}/Rad21l^{tm1b(KOMP)Wtsi} Rec8^{tm1b(KOMP)Wtsi}/Rec8^{tm1b(KOMP)Wtsi} B6N(Cg)-Rad21l^{tm1b(KOMP)Wtsi} Rec8^{tm1b(KOMP)Wtsi}	abnormal double-strand DNA break repair	J:280261
Rad21l^{tm1b(KOMP)Wtsi}/Rad21l^{tm1b(KOMP)Wtsi} Stag3^{tm1e.1(KOMP)Wtsi}/Stag3^{tm1e.1(KOMP)Wtsi} B6N(Cg)-Rad21l^{tm1b(KOMP)Wtsi} Stag3^{tm1e.1(KOMP)Wtsi}	abnormal double-strand DNA break repair	J:280261
	abnormal synaptonemal complex	J:280261
Rad21l^tm1Yow/Rad21l^tm1Yow Rec8^mei8/Rec8^mei8 involves: 129S4/SvJae * C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj	abnormal male meiosis	J:209347
	abnormal meiosis	J:209347
Rad21l^tm1Yow/Rad21l^tm1Yow Spo11^tm1Mjn/Spo11^tm1Mjn involves: 129X1/SvJ * C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj	abnormal chromosomal synapsis	J:209347
	abnormal male meiosis	J:209347
	abnormal synaptonemal complex	J:209347
Rad21l^tm1Yow/Rad21l^tm1Yow Sun1^tm1Mhan/Sun1^tm1Mhan involves: 129S6/SvEvTac * C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj	abnormal chromosomal synapsis	J:209347
	abnormal male meiosis	J:209347

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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