Ift57 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Ift57
intraflagellar transport 57
MGI:1921166

19 phenotypes from 2 alleles in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Ift57^tm1Dwni/Ift57^tm1Dwni involves: 129S1/SvImJ * C57BL/6J	abnormal cranial flexure morphology	J:119664
	abnormal direction of embryo turning	J:119664
	abnormal direction of heart looping	J:119664
	abnormal left-right axis patterning	J:119664
	abnormal maxilla morphology	J:119664
	abnormal neural tube morphology	J:119664
	abnormal spinal cord morphology	J:119664
	absent embryonic cilia	J:119664
	absent floor plate	J:119664
	delayed embryo turning	J:119664
	embryonic growth retardation	J:119664
	embryonic lethality during organogenesis, incomplete penetrance	J:119664
	exencephaly	J:119664
	failure of initiation of embryo turning	J:119664
	incomplete rostral neuropore closure	J:119664
	ocular hypotelorism	J:119664
	open neural tube	J:119664
	pericardial edema	J:119664
	polydactyly	J:119664
Ift57^tm2Dwni/Ift57^tm2Dwni involves: 129S1/SvImJ * C57BL/6J	abnormal cranial flexure morphology	J:119664
	abnormal direction of embryo turning	J:119664
	abnormal direction of heart looping	J:119664
	abnormal left-right axis patterning	J:119664
	abnormal maxilla morphology	J:119664
	abnormal neural tube morphology	J:119664
	abnormal spinal cord morphology	J:119664
	absent embryonic cilia	J:119664
	absent floor plate	J:119664
	delayed embryo turning	J:119664
	embryonic growth retardation	J:119664
	embryonic lethality during organogenesis, incomplete penetrance	J:119664
	exencephaly	J:119664
	failure of initiation of embryo turning	J:119664
	incomplete rostral neuropore closure	J:119664
	ocular hypotelorism	J:119664
	open neural tube	J:119664
	pericardial edema	J:119664
	polydactyly	J:119664

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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