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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Slfn14
schlafen 14
MGI:2684866
24 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Slfn14em1(IMPC)Tcp/Slfn14em1(IMPC)Tcp
C57BL/6NCrl-Slfn14em1(IMPC)Tcp/Tcp
abnormal lens morphology J:211773
abnormal retina blood vessel morphology J:211773
abnormal retina vasculature morphology J:211773
abnormal stomach morphology J:211773
decreased hematocrit J:211773
decreased mean corpuscular volume J:211773
increased mean corpuscular hemoglobin J:211773
increased mean corpuscular hemoglobin concentration J:211773
increased mean platelet volume J:211773
increased red blood cell distribution width J:211773
Slfn14em1Nvm/Slfn14+
C57BL/6J-Slfn14em1Nvm
abnormal erythropoiesis J:325381
abnormal platelet morphology J:325381
abnormal proerythroblast morphology J:325381
abnormal thrombosis J:325381
decreased hemoglobin content J:325381
enlarged spleen J:325381
extramedullary hematopoiesis J:325381
hemolytic anemia J:325381
increased erythrocyte cell number J:325381
increased mean platelet volume J:325381
increased megakaryocyte-erythroid progenitor cell number J:325381
increased spleen weight J:325381
microcytosis J:325381
Slfn14em1Nvm/Slfn14em1Nvm
C57BL/6J-Slfn14em1Nvm
abnormal vascular development J:325381
postnatal lethality, complete penetrance J:325381

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
04/23/2024
MGI 6.23
The Jackson Laboratory