Nosip Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Nosip
nitric oxide synthase interacting protein
MGI:1913644

38 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Nosip^em1(IMPC)Tcp/Nosip⁺ C57BL/6NCrl-Nosip^em1(IMPC)Tcp/Tcp	abnormal lens morphology	J:211773
	abnormal retina blood vessel morphology	J:211773
	abnormal retina vasculature morphology	J:211773
	cataract	J:211773
	thrombocytosis	J:211773
Nosip^em1(IMPC)Tcp/Nosip^em1(IMPC)Tcp C57BL/6NCrl-Nosip^em1(IMPC)Tcp/Tcp	abnormal embryo size	J:211773
	edema	J:211773
	preweaning lethality, complete penetrance	J:211773
Nosip^{Gt(OST138992)Lex}/Nosip^{Gt(OST138992)Lex} B6.129S5-Nosip^{Gt(OST138992)Lex}	abnormal craniofacial morphology	J:245546
	abnormal lateral ganglionic eminence morphology	J:245546
	abnormal lens morphology	J:245546
	abnormal medial ganglionic eminence morphology	J:245546
	abnormal midface morphology	J:245546
	abnormal palate morphology	J:245546
	abnormal telencephalon development	J:245546
	absent basisphenoid bone	J:245546
	absent nasopharynx	J:245546
	absent olfactory bulb	J:245546
	absent telencephalon	J:245546
	agnathia	J:245546
	anophthalmia	J:245546
	cleft secondary palate	J:245546
	coloboma	J:245546
	cyanosis	J:245546
	cyclopia	J:245546
	decreased embryo weight	J:245546
	decreased fetal weight	J:245546
	dilated lateral ventricle	J:245546
	enlarged third ventricle	J:245546
	exencephaly	J:245546
	holoprosencephaly	J:245546
	microphthalmia	J:245546
	midline facial cleft	J:245546
	narrow snout	J:245546
	ocular hypotelorism	J:245546
	olfactory bulb hypoplasia	J:245546
	perinatal lethality, complete penetrance	J:245546
	proboscis	J:245546
	respiratory distress	J:245546

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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