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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Ror1
receptor tyrosine kinase-like orphan receptor 1
MGI:1347520
17 phenotypes from 2 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Ror1tm1.2Meg/Ror1tm1.2Meg
involves: 129S4/SvJae * C57BL/6 * FVB/N
exencephaly J:182150
Ror1tm1Ymi/Ror1tm1Ymi
involves: 129P2/OlaHsd
abnormal axon fasciculation J:232175
abnormal cochlea morphology J:232175
abnormal cochlear hair cell morphology J:232175
abnormal distortion product otoacoustic emission J:232175
abnormal ribbon synapse morphology J:232175
abnormal sensory neuron innervation pattern J:232175
abnormal synapse morphology J:232175
deafness J:232175
decreased cochlear coiling J:232175
increased or absent threshold for auditory brainstem response J:232175
Ror1tm1Ymi/Ror1tm1Ymi
involves: 129P2/OlaHsd * C57BL/6
abnormal blood homeostasis J:72948
abnormal pulmonary alveolus morphology J:72948
abnormal respiratory system physiology J:72948
cyanosis J:72948
neonatal lethality, complete penetrance J:72948
respiratory distress J:72948

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
11/14/2017
MGI 6.11
The Jackson Laboratory