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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Sptan1
spectrin alpha, non-erythrocytic 1
MGI:98386
20 phenotypes from 2 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Sptan1Gt(RRQ171)Byg/Sptan1Gt(RRQ171)Byg
B6.129P2-Sptan1Gt(RRQ171)Byg
abnormal cell physiology J:186305
abnormal cortical ventricular zone morphology J:186305
abnormal craniofacial morphology J:186305
abnormal embryonic/fetal subventricular zone morphology J:186305
abnormal forebrain morphology J:186305
abnormal heart shape J:186305
abnormal lateral ventricle morphology J:186305
abnormal neural tube closure J:186305
cerebral aqueductal stenosis J:186305
decreased embryo size J:186305
dilated brain ventricles J:186305
dilated heart J:186305
embryonic growth retardation J:186305
embryonic lethality during organogenesis, incomplete penetrance J:186305
increased cell proliferation J:186305
lethality throughout fetal growth and development, complete penetrance J:186305
thin myocardium compact layer J:186305
Sptan1Gt(RRQ171)Byg/Sptan1Gt(RRQ171)Byg
involves: 129P2/OlaHsd
abnormal axon initial segment morphology J:186168
Sptan1tm1.1Gnic/Sptan1tm1.1Gnic
either: (involves: 129/Sv) or (involves: 129/Sv * C57BL/6)
normal cellular phenotype J:122549
no abnormal phenotype detected J:122549

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
08/06/2019
MGI 6.14
The Jackson Laboratory