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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
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Allelic Composition
Genetic Background
Annotated Term Reference
Ift57tm1Dwni/Ift57tm1Dwni
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
Ift57tm2Dwni/Ift57tm2Dwni
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

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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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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory