Nobox Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Nobox
NOBOX oogenesis homeobox
MGI:108011

16 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Nobox^{tm1.1(KOMP)Vlcg}/Nobox⁺ C57BL/6N-Nobox^{tm1.1(KOMP)Vlcg}/Ucd	abnormal embryo size	J:211773
	decreased fasting circulating glucose level	J:211773
	embryonic growth retardation	J:211773
	hyperactivity	J:211773
Nobox^{tm1.1(KOMP)Vlcg}/Nobox^{tm1.1(KOMP)Vlcg} C57BL/6N-Nobox^{tm1.1(KOMP)Vlcg}/Ucd	abnormal seminal vesicle morphology	J:211773
	preweaning lethality, incomplete penetrance	J:211773
Nobox^tm1Rajk/Nobox^tm1Rajk involves: 129S7/SvEvBrd * C57BL/6	abnormal oocyte morphology	J:92421
	abnormal ovarian follicle number	J:92421
	absent oocytes	J:92421
	absent secondary ovarian follicles	J:92421
	decreased oocyte number	J:92421
	female infertility	J:92421
	impaired ovarian folliculogenesis	J:92421
	oocyte degeneration	J:92421
	ovary atrophy	J:92421
	ovary cyst	J:92421

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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