Ninj1 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Ninj1
ninjurin 1
MGI:1196617

12 phenotypes from 3 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Ninj1^{tm1a(KOMP)Wtsi}/Ninj1⁺ involves: C57BL/6N	no abnormal phenotype detected	J:197409
Ninj1^{tm1b(KOMP)Wtsi}/Ninj1⁺ involves: C57BL/6N * FVB/N	increased cellular sensitivity to gamma-irradiation	J:197409
Ninj1^{tm1b(KOMP)Wtsi}/Ninj1^{tm1b(KOMP)Wtsi} involves: C57BL/6N * FVB/N	abnormal cellular replicative senescence	J:197409
	hydrocephaly	J:197409
	premature death	J:197409
Ninj1^tm1Gto/Ninj1⁺ B6.129P2-Ninj1^tm1Gto	decreased susceptibility to experimental autoimmune encephalomyelitis	J:209516
Ninj1^tm1Gto/Ninj1^tm1Gto B6.129P2-Ninj1^tm1Gto	abnormal leukocyte adhesion	J:209516
	abnormal leukocyte physiology	J:209516
	ataxia	J:209516
	decreased susceptibility to experimental autoimmune encephalomyelitis	J:209516
	normal hematopoietic system phenotype	J:209516
	hydrocephaly	J:209516
	impaired macrophage chemotaxis	J:209516
	postnatal growth retardation	J:209516

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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