Trip11 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Trip11
thyroid hormone receptor interactor 11
MGI:1924393

35 phenotypes from 3 alleles in 4 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Trip11^{Gt(AJ0490)Wtsi}/Trip11^{Gt(AJ0490)Wtsi} involves: 129P2/OlaHsd * C57BL/6	abnormal cell morphology	J:142875
	abnormal craniofacial morphology	J:142875
	abnormal lung saccule morphology	J:142875
	abnormal lung vasculature morphology	J:142875
	abnormal pulmonary alveolus epithelial cell morphology	J:142875
	abnormal type I pneumocyte morphology	J:142875
	cyanosis	J:142875
	decreased fetal weight	J:142875
	decreased locomotor activity	J:142875
	heart right ventricle outflow tract stenosis	J:142875
	muscular ventricular septal defect	J:142875
	neonatal lethality, complete penetrance	J:142875
	omphalocele	J:142875
	overriding aortic valve	J:142875
	small lung saccule	J:142875
	thick ventricular wall	J:142875
Trip11^m1Mawa/Trip11^m1Mawa C57BL/6J-Trip11^m1Mawa	abnormal bone mineralization	J:163656
	abnormal cell physiology	J:163656
	abnormal chondrocyte morphology	J:163656
	abnormal chondrocyte physiology	J:163656
	abnormal endoplasmic reticulum morphology	J:163656
	abnormal long bone epiphysis morphology	J:163656
	abnormal osteoblast morphology	J:163656
	abnormal pulmonary alveolus morphology	J:163656
	domed cranium	J:163656
	failure of bone ossification	J:163656
	neonatal lethality, complete penetrance	J:163656
	omphalocele	J:163656
	short limbs	J:163656
	short snout	J:163656
	small thoracic cage	J:163656
Trip11^m1Mawa/Trip11^m1Mawa Tg(Mbp-MAPT/lacZ)#aCaw/Tg(Mbp-MAPT/lacZ)#aCaw involves: BALB/c * C57BL/6 * C57BL/6J * FVB/N	abnormal cerebral cortex morphology	J:168258
	decreased brain size	J:168258
	normal nervous system phenotype	J:168258
	omphalocele	J:168258
	postnatal lethality, complete penetrance	J:168258
	short limbs	J:168258
	small olfactory bulb	J:168258
Trip11^tm1.1Psmi/Trip11^tm1.1Psmi B6;129S-Trip11^tm1.1Psmi/Psmi	no abnormal phenotype detected	J:253969

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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