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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Stxbp1
syntaxin binding protein 1
MGI:107363
21 phenotypes from 3 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Stxbp1tm1b(EUCOMM)Hmgu/Stxbp1+
C57BL/6N-Stxbp1tm1b(EUCOMM)Hmgu/J
abnormal auditory brainstem response J:211773
decreased hematocrit J:211773
hyperactivity J:211773
impaired glucose tolerance J:211773
increased exploration in new environment J:211773
increased grip strength J:211773
increased mean corpuscular volume J:211773
increased thigmotaxis J:211773
Stxbp1tm1b(EUCOMM)Hmgu/Stxbp1tm1b(EUCOMM)Hmgu
C57BL/6N-Stxbp1tm1b(EUCOMM)Hmgu/J
abnormal embryo size J:211773
edema J:211773
hemorrhage J:211773
preweaning lethality, complete penetrance J:211773
Stxbp1tm1Mver/Stxbp1tm1Mver
Tg(Pcp2-cre)2Mpin/0
involves: 129S1/Sv * 129X1/SvJ
ataxia J:100337
decreased Purkinje cell number J:100337
Stxbp1tm1Sud/Stxbp1tm1Sud
Not Specified
abnormal neurotransmitter secretion J:77237, J:100337
abnormal synaptic transmission J:77237
axon degeneration J:85723
neonatal lethality, complete penetrance J:77237
normal nervous system phenotype J:77237
neurodegeneration J:77237
neuron degeneration J:100337

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
04/23/2024
MGI 6.23
The Jackson Laboratory