Ocrl Phenotype Annotations - Multigenic Genotypes

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Ocrl
OCRL, inositol polyphosphate-5-phosphatase
MGI:109589

12 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Inpp5b^tm1Nbm/Inpp5b^tm1Nbm Ocrl^tm1Nbm/Ocrl^tm1Nbm either: (involves: 129S/SvEv * 129S6/SvEvTac * C57BL/6) or (involves: 129S/SvEv * 129S6/SvEvTac * C57BL/6 * NIH Black Swiss) or (involves: 129S/SvEv * 129S6/SvEvTac * NIH Black Swiss)	embryonic lethality during organogenesis, complete penetrance	J:47884
Inpp5b^tm1Nbm/Inpp5b^tm1Nbm Ocrl^tm1Nbm/Ocrl^tm1Nbm Tg(INPP5B)CNbm/0 involves: 129S/SvEv * 129S6/SvEvTac * FVB/N	aminoaciduria	J:185879
	decreased birth body size	J:185879
	decreased body weight	J:185879
	increased urine microglobulin level	J:185879
	postnatal growth retardation	J:185879
	premature death	J:185879
	normal vision/eye phenotype	J:185879
Inpp5b^tm1Nbm/Inpp5b^tm1Nbm Ocrl^tm1Nbm/Ocrl^tm1Nbm Tg(INPP5B)CNbm/Tg(INPP5B)CNbm involves: 129S/SvEv * 129S6/SvEvTac * FVB/N	decreased body weight	J:185879
	postnatal growth retardation	J:185879
	normal renal/urinary system phenotype	J:185879
Inpp5b^tm1Nbm/Inpp5b^tm1Nbm Ocrl^tm1Nbm/Y Tg(INPP5B)CNbm/0 involves: 129S/SvEv * 129S6/SvEvTac * FVB/N	aminoaciduria	J:185879
	decreased birth body size	J:185879
	decreased body weight	J:185879
	increased urine microglobulin level	J:185879
	postnatal growth retardation	J:185879
	premature death	J:185879
	normal vision/eye phenotype	J:185879
Inpp5b^tm1Nbm/Inpp5b^tm1Nbm Ocrl^tm1Nbm/Y Tg(INPP5B)CNbm/Tg(INPP5B)CNbm involves: 129S/SvEv * 129S6/SvEvTac * FVB/N	decreased body weight	J:185879
	postnatal growth retardation	J:185879
	normal renal/urinary system phenotype	J:185879
Ocrl^tm2Nbm/Y either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * NIH Black Swiss)	normal homeostasis/metabolism phenotype	J:47884
	normal mortality/aging	J:47884
	normal reproductive system phenotype	J:47884
	normal vision/eye phenotype	J:47884
Ocrl^tm2Nbm/Ocrl^tm2Nbm either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * NIH Black Swiss)	normal homeostasis/metabolism phenotype	J:47884
	normal mortality/aging	J:47884
	normal reproductive system phenotype	J:47884
	normal vision/eye phenotype	J:47884

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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