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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Mfsd2b
MFSD2 lysolipid transporter B, sphingolipid
MGI:3583946
18 phenotypes from 1 allele in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Mfsd2btm1a(KOMP)Wtsi/Mfsd2btm1a(KOMP)Wtsi
B6JTyr;B6N-Mfsd2btm1a(KOMP)Wtsi/Wtsi
decreased circulating iron level J:175295
decreased erythrocyte cell number J:175295
increased mean corpuscular hemoglobin J:175295
Mfsd2btm1a(KOMP)Wtsi/Mfsd2btm1a(KOMP)Wtsi
C57BL/6-Mfsd2btm1a(KOMP)Wtsi
abnormal ceramide level J:250123
abnormal mean corpuscular volume J:250123
abnormal stress erythropoiesis J:250123
decreased B cell number J:250123
decreased erythrocyte cell number J:250123
decreased leukocyte cell number J:250123
decreased sphingosine level J:250123
decreased T cell number J:250123
enlarged spleen J:250123
normal hematopoietic system phenotype J:250123
hemolysis J:250123
normal homeostasis/metabolism phenotype J:250123
increased sphingosine level J:250123
increased susceptibility to type I hypersensitivity reaction J:250123
reticulocytopenia J:250123
stomatocytosis J:250123

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
07/02/2024
MGI 6.13
The Jackson Laboratory