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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Slc2a1
solute carrier family 2 (facilitated glucose transporter), member 1
MGI:95755
13 phenotypes from 3 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Slc2a1em1Mase/Slc2a1em1Mase
involves: C57BL/6N
postnatal lethality, complete penetrance J:308608
Slc2a1Rgsc200/Slc2a1+
involves: C57BL/6JJcl * DBA/2JJcl
ataxia J:133634
impaired passive avoidance behavior J:133634
no spontaneous movement J:133634
Slc2a1tm1Dcdv/Slc2a1+
involves: 129S6/SvEvTac * C57BL/6J
abnormal glucose homeostasis J:108250
abnormal motor capabilities/coordination/movement J:108250
decreased brain weight J:108250
decreased cellular glucose uptake J:108250
impaired coordination J:108250
sporadic seizures J:108250
Slc2a1tm1Dcdv/Slc2a1tm1Dcdv
involves: 129S6/SvEvTac * C57BL/6J
decreased embryo size J:108250
embryonic growth retardation J:108250
embryonic lethality during organogenesis, complete penetrance J:108250

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
04/16/2024
MGI 6.23
The Jackson Laboratory