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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Pml
promyelocytic leukemia
MGI:104662
17 phenotypes from 2 alleles in 4 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Pmltm1.1Ews/Pmltm1.1Ews
FVB.129P2-Pmltm1.1Ews
abnormal double-strand DNA break repair J:262172
abnormal PML bodies J:262172
elevated level of mitotic sister chromatid exchange J:262172
increased cellular sensitivity to ionizing radiation J:262172
increased hematopoietic stem cell number J:262172
normal neoplasm J:262172
Pmltm1.1Ews/Pmltm1.1Ews
involves: 129 * 129P2/OlaHsd
increased B cell derived lymphoma incidence J:262172
increased T cell derived lymphoma incidence J:262172
Pmltm1Ppp/Pmltm1Ppp
FVB.129S7-Pmltm1Ppp
abnormal double-strand DNA break repair J:262172
increased hematopoietic stem cell number J:262172
Pmltm1Ppp/Pmltm1Ppp
involves: 129S7/SvEvBrd
abnormal cell physiology J:46381
abnormal immune system cell morphology J:46381
abnormal myelopoiesis J:46381
decreased granulocyte number J:46381
decreased leukocyte cell number J:46381
increased fibroblast proliferation J:46381
increased lymphoma incidence J:46381
increased susceptibility to bacterial infection J:46381
increased tumor incidence J:46381

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