Rttn Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Rttn
rotatin
MGI:2179288

21 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Rttn^em1(IMPC)Tcp/Rttn⁺ C57BL/6NCrl-Rttn^em1(IMPC)Tcp/Tcp	abnormal liver morphology	J:211773
	abnormal skin morphology	J:211773
	abnormal spleen morphology	J:211773
	abnormal stomach morphology	J:211773
	cataract	J:211773
	decreased bone mineral content	J:211773
	enlarged urinary bladder	J:211773
	small heart	J:211773
Rttn^em1(IMPC)Tcp/Rttn^em1(IMPC)Tcp C57BL/6NCrl-Rttn^em1(IMPC)Tcp/Tcp	abnormal embryo size	J:211773
	embryonic growth retardation	J:211773
	prenatal lethality prior to heart atrial septation	J:211773
	preweaning lethality, complete penetrance	J:211773
Rttn^{Gt(pGT1.8geo)7Pgr}/Rttn^{Gt(pGT1.8geo)7Pgr} involves: 129S1/Sv * 129X1/SvJ * NMRI	abnormal direction of heart looping	J:76233
	abnormal embryo turning	J:76233
	abnormal neural tube morphology	J:76233
	abnormal somite development	J:76233
	decreased embryo size	J:76233
	embryonic lethality during organogenesis, complete penetrance	J:76233
	failure of initiation of embryo turning	J:76233
	notochord degeneration	J:76233
	pericardial effusion	J:76233

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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