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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Sptbn2
spectrin beta, non-erythrocytic 2
MGI:1313261
18 phenotypes from 3 alleles in 4 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Sptbn2Gt(XK442)Byg/Sptbn2+
involves: 129P2/OlaHsd * C57BL/6J
impaired coordination J:158494
Sptbn2Gt(XK442)Byg/Sptbn2Gt(XK442)Byg
involves: 129P2/OlaHsd * C57BL/6J
abnormal cerebellar molecular layer J:158494
abnormal Purkinje cell dendrite morphology J:158494
abnormal Purkinje cell morphology J:158494
ataxia J:158494
clonic seizures J:158494
increased body weight J:158494
thin cerebellar molecular layer J:158494
Sptbn2tm1b(EUCOMM)Hmgu/Sptbn2tm1b(EUCOMM)Hmgu
C57BL/6N-Sptbn2tm1b(EUCOMM)Hmgu/H
decreased circulating chloride level J:211773
short tibia J:211773
Sptbn2tm1Mjac/Sptbn2+
involves: 129P2/OlaHsd
normal behavior/neurological phenotype J:163169
normal nervous system phenotype J:163169
Sptbn2tm1Mjac/Sptbn2tm1Mjac
B6.129P2-Sptbn2tm1Mjac
abnormal gait J:159622
abnormal nervous system electrophysiology J:159622
ataxia J:159622
impaired balance J:159622
impaired coordination J:159622
increased excitatory postsynaptic current amplitude J:159622
Purkinje cell degeneration J:159622
tremors J:159622

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
10/10/2017
MGI 6.10
The Jackson Laboratory