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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Mycbp2
MYC binding protein 2, E3 ubiquitin protein ligase
MGI:2179432
42 phenotypes from 7 alleles in 10 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Emx1tm1(cre)Krj/Emx1+
Mycbp2tm1Adia/Mycbp2tm1Adia
involves: 129S2/SvPas * C57BL/6
abnormal axon guidance J:125702
abnormal corpus callosum morphology J:125702
abnormal hippocampus morphology J:125702
decreased corpus callosum size J:125702
enlarged lateral ventricles J:125702
Mnx1tm4(cre)Tmj/Mnx1+
Mycbp2tm1Adia/Mycbp2tm1Adia
involves: 129S1/Sv * C57BL/6
abnormal neuromuscular synapse morphology J:125702
perinatal lethality, incomplete penetrance J:125702
normal respiratory system phenotype J:125702
Mycbp2em1(IMPC)Mbp/Mycbp2+
C57BL/6N-Mybpc2em1(IMPC)Mbp/Ucd
abnormal eye morphology J:211773
abnormal heart morphology J:211773
anophthalmia J:211773
enlarged heart J:211773
Mycbp2em1(IMPC)Mbp/Mycbp2em1(IMPC)Mbp
C57BL/6N-Mybpc2em1(IMPC)Mbp/Ucd
preweaning lethality, complete penetrance J:211773
Mycbp2m274-4Tpo/Mycbp2m274-4Tpo
involves: C57BL/6J * SSL/LeJ
decreased birth body size J:149893
decreased birth weight J:149893
hunched posture J:149893
neonatal lethality, complete penetrance J:149893
respiratory distress J:149893
Mycbp2magsp/Mycbp2magsp
Tg(Isl1-EGFP*)1Slp/0
B6.Cg-Mycbp2magsp Tg(Isl1-EGFP*)1Slp
abnormal motor neuron innervation pattern J:132726
Mycbp2mgln/Mycbp2mgln
Tg(Isl1-EGFP)2Slp/0
involves: C3H * C57BL/6 * DBA/2J
abnormal motor neuron innervation pattern J:132726
Mycbp2mgln/Mycbp2mgln
Tg(Isl1-EGFP*)1Slp/0
B6.Cg-Mycbp2mgln Tg(Isl1-EGFP*)1Slp
abnormal axon extension J:132726
abnormal motor neuron innervation pattern J:132726
abnormal motor neuron morphology J:132726
abnormal sensory neuron innervation pattern J:132726
abnormal sensory neuron morphology J:132726
abnormal spinal nerve morphology J:132726
Mycbp2mgln/Mycbp2mgln
Tg(Mnx1-GFP)1Slp/0
involves: C3H * C57BL/6 * DBA/2J
abnormal motor neuron innervation pattern J:132726
Mycbp2tm1.1Adia/Mycbp2tm1.1Adia
involves: C57BL/6 * FVB/N
abnormal axon guidance J:125702
abnormal brain internal capsule morphology J:125702
abnormal brain interneuron morphology J:125702
abnormal brain morphology J:125702
abnormal diaphragm morphology J:125702
abnormal diencephalon morphology J:125702
abnormal habenula morphology J:125702
abnormal hippocampus morphology J:125702
abnormal innervation J:125702
abnormal lateral geniculate nucleus morphology J:125702
abnormal midbrain morphology J:125702
abnormal motor neuron morphology J:125702
abnormal nervous system morphology J:125702
abnormal neuromuscular synapse morphology J:125702
abnormal phrenic nerve morphology J:125702
abnormal thalamus morphology J:125702
absent anterior commissure J:125702
decreased corpus callosum size J:125702
dilated lateral ventricle J:125702
loss of cortex neurons J:125702
neonatal lethality, complete penetrance J:125702
Mycbp2tm1.1Klsc/Mycbp2tm1.1Klsc
Tg(Nes-cre)1Kln/0
involves: C57BL/6 * SJL
abnormal survival J:168745
Mycbp2tm1.1Klsc/Mycbp2tm1.1Klsc
Tg(Scn10a-cre)1Rkun/0
involves: C57BL/6 * DBA/2
abnormal spinal cord morphology J:168745
decreased thermal nociceptive threshold J:168745

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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last database update
04/30/2024
MGI 6.23
The Jackson Laboratory