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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Sptbn4
spectrin beta, non-erythrocytic 4
MGI:1890574
39 phenotypes from 15 alleles in 18 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Sptbn4Gt(ROSABetageo)62Sor/Sptbn4Gt(ROSABetageo)62Sor
129S4/SvJaeSor-Spnb4Gt(ROSABetageo)62Sor
abnormal muscle contractility J:77228
ataxia J:77228
limb grasping J:77228
tremors J:77228
Sptbn4Gt(ROSABetageo)62Sor/Sptbn4Gt(ROSABetageo)62Sor
B6.129S4-Sptbn4Gt(ROSABetageo)62Sor/Mmucd
abnormal muscle contractility J:77228
ataxia J:77228
limb grasping J:77228
tremors J:77228
Sptbn4Gt(ROSABetageo)62Sor/Sptbn4Gt(ROSABetageo)62Sor
involves: 129S4/SvJaeSor * C57BL/6J
abnormal axon morphology J:120916
abnormal mating frequency J:77228
abnormal muscle contractility J:77228, J:120916
abnormal myelination J:120916
ataxia J:77228
limb grasping J:77228
tremors J:77228
Sptbn4qv-2J/Sptbn4qv-2J
CXB6/By Sptbn4qv-2J
abnormal auditory brainstem response J:14995
Sptbn4qv-3J/Sptbn4qv-3J
C57BL/6J-Sptbnqv-3J/J
abnormal auditory brainstem response J:14995
absent linear vestibular evoked potential J:116914
tremors J:116914
Sptbn4qv-4J/Sptbn4qv-4J
involves: C57BL/6J * CBA/CaJ * DBA/2J
abnormal auditory brainstem response waveform shape J:71549
increased or absent threshold for auditory brainstem response J:71549
Sptbn4qv-7J/Sptbn4qv-7J
A.B6 Tyr+-Sptbn4qv-7J/J
normal muscle phenotype J:82238
paraparesis J:82238
Sptbn4qv-8J/Sptbn4qv-8J
C57BL/6J-Sptbn4qv-8J/J
tremors J:82238
Sptbn4qv-9J/Sptbn4qv-9J
involves: BALB/cByJ * C57BL/6J
abnormal posture J:87349
head bobbing J:87349
increased vertical activity J:87349
limb grasping J:87349
tremors J:87349
Sptbn4qv-10J/Sptbn4qv-10J
involves: BALB/cJ * C57BL/6J
abnormal gait J:137504
ataxia J:137504
deafness J:137504
impaired balance J:137504
increased or absent threshold for auditory brainstem response J:137504
male infertility J:137504
normal mortality/aging J:137504
tremors J:137504
normal vision/eye phenotype J:137504
Sptbn4qv-11J/Sptbn4qv-11J
C57BL/6J-Sptbn4qv-11J/J
abnormal gait J:137504
impaired hearing J:137504
increased or absent threshold for auditory brainstem response J:137504
male infertility J:137504
normal mortality/aging J:137504
tremors J:137504
Sptbn4qv-J/Sptbn4qv-J
C3FeB6 A/Aw-J-Sptbn4qv-J/J
normal muscle phenotype J:37678
tremors J:20207
Sptbn4qv-lnd2J/Sptbn4+
C3H/HeJ-Sptbn4qv-lnd2J/J
reduced linear vestibular evoked potential J:116914
Sptbn4qv-lnd2J/Sptbn4qv-lnd2J
C3H/HeJ-Sptbn4qv-lnd2J/J
abnormal auditory brainstem response waveform shape J:71549
abnormal auditory cortex morphology J:71549
absent linear vestibular evoked potential J:116914
increased or absent threshold for auditory brainstem response J:71549
premature death J:30329
Sptbn4qv-lnd/Sptbn4qv-lnd
B6.B10-Sptbn4qv-lnd
abnormal gait J:11718
axonal dystrophy J:11718
decreased body size J:11718
male infertility J:11718
paresis J:11718
tremors J:11718
Sptbn4qv/Sptbn4qv
either: (involves: BALB/c) or (involves: C57BL/10)
ataxia J:167
deafness J:167
eye inflammation J:167
hindlimb paralysis J:167
male infertility J:167
paralysis J:167
premature death J:167
priapism J:167
tremors J:167
Sptbn4qv/Sptbn4qv
involves: CBA/Gr
abnormal auditory brainstem response J:71549
Sptbn4qv/Sptbn4qv
Not Specified
deafness J:32693
Sptbn4tm1Mkom/Sptbn4tm1Mkom
involves: 129S4/SvJaeSor * C57BL/6J
abnormal axon morphology J:120916
abnormal myelination J:120916
normal reproductive system phenotype J:120916
tremors J:120916
Sptbn4tm1Msol/Sptbn4tm1Msol
involves: C57BL/6
abnormal auditory brainstem response J:93411
abnormal cerebellum morphology J:93411
abnormal gait J:93411
abnormal optic nerve morphology J:93411
abnormal sciatic nerve morphology J:93411
decreased body weight J:93411
dysmetria J:93411
tremors J:93411

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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
11/19/2024
MGI 6.24
The Jackson Laboratory