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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Kif1b
kinesin family member 1B
MGI:108426
31 phenotypes from 3 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Kif1bGt(XC445)Byg/Kif1bGt(XC445)Byg
B6.129P2-Kif1bGt(XC445)Byg
embryonic lethality J:94077
Kif1btm1b(KOMP)Wtsi/Kif1b+
C57BL/6N-Kif1btm1b(KOMP)Wtsi/J
abnormal behavioral response to light J:211773
cyanosis J:211773
decreased circulating glucose level J:211773
hyperactivity J:211773
increased circulating chloride level J:211773
increased circulating glucose level J:211773
increased circulating sodium level J:211773
increased mean corpuscular hemoglobin concentration J:211773
Kif1btm1b(KOMP)Wtsi/Kif1btm1b(KOMP)Wtsi
C57BL/6N-Kif1btm1b(KOMP)Wtsi/J
abnormal embryo size J:211773
abnormal facial morphology J:211773
abnormal head shape J:211773
abnormal limb morphology J:211773
abnormal outer ear morphology J:211773
hemorrhage J:211773
preweaning lethality, complete penetrance J:211773
Kif1btm1Noh/Kif1b+
involves: 129S4/SvJae * C57BL/6J
abnormal axonal transport J:69772
abnormal motor coordination/balance J:69772
impaired coordination J:69772
progressive muscle weakness J:69772
Kif1btm1Noh/Kif1btm1Noh
involves: 129S4/SvJae * C57BL/6J
abnormal brain commissure morphology J:69772
abnormal brainstem morphology J:69772
abnormal hippocampus morphology J:69772
abnormal spinal cord ventral horn morphology J:69772
abnormal synaptic vesicle number J:69772
decreased brain size J:69772
decreased neuron number J:69772
lordosis J:69772
neonatal lethality, complete penetrance J:69772
respiratory failure J:69772
unresponsive to tactile stimuli J:69772

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
07/31/2018
MGI 6.12
The Jackson Laboratory