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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Prom2
prominin 2
MGI:2138997
16 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Prom2tm1.1(KOMP)Vlcg/Prom2+
C57BL/6N-Prom2tm1.1(KOMP)Vlcg/J
abnormal retina morphology J:211773
decreased circulating calcium level J:211773
decreased circulating iron level J:211773
decreased grip strength J:211773
hyperactivity J:211773
increased circulating alanine transaminase level J:211773
increased circulating aspartate transaminase level J:211773
increased circulating potassium level J:211773
Prom2tm1.1(KOMP)Vlcg/Prom2tm1.1(KOMP)Vlcg
C57BL/6N-Prom2tm1.1(KOMP)Vlcg/J
abnormal nail morphology J:211773
abnormal retina morphology J:211773
abnormal sleep behavior J:211773
decreased grip strength J:211773
hyperactivity J:211773
increased hemoglobin content J:211773
increased mean corpuscular hemoglobin concentration J:211773
Prom2tm1Lex/Prom2tm1Lex
B6;129S5-Prom2tm1Lex/Mmucd
anemia J:171883
decreased erythrocyte cell number J:171883
decreased hematocrit J:171883
decreased mean corpuscular hemoglobin J:171883

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
12/10/2024
MGI 6.24
The Jackson Laboratory