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Symbol
Name
ID
Myc
myelocytomatosis oncogene
MGI:97250
Phenotype annotations related to cellular
Darker colors indicate more annotations
Human Phenotypes
Gangrene
Disease(s) Associated with MYC
acute promyelocytic leukemia

Mouse Phenotypes
abnormal intestinal goblet cell morphology
abnormal intracellular organelle morphology
abnormal cell nucleus morphology
binucleate
abnormal chromosome number
aneuploidy
polyploidy
abnormal hepatocyte mitochondrial morphology
abnormal cell cycle
abnormal mitosis
increased B cell apoptosis
increased male germ cell apoptosis
focal hepatic necrosis
decreased B cell proliferation
increased B cell proliferation
decreased T cell proliferation
abnormal enterocyte proliferation
decreased fibroblast proliferation
absent fibroblast proliferation
decreased cell proliferation
chromosomal instability
induced chromosome breakage
spontaneous chromosome breakage
Availability Mouse Genotype
Bmyctm1Mpo/Bmyctm1Mpo
Myctm1.1Itl/Myctm1.1Itl
Myctm1Atp/Myctm1Atp
Myctm1Jlc/Myctm1Jlc
Myctm1Lbox/Myctm1Lbox
Myctm4.1Fwa/Myctm4.1Fwa
Tg(HBVX*,-Myc)#Skp/Tg(HBVX*,-Myc)#Skp
Myctm1Atp/Myc+
Myctm1Atp/Myctm2.1Atp
Myctm2.1Atp/Myc+
Myctm37Mnz/Myc+
Myctm39Mnz/Myc+
Tg(IghMyc)22Bri/0
Tg(IghMyc)186Brn/0
Gt(ROSA)26Sortm1(Myc)Rcse/Gt(ROSA)26Sortm1(Myc)Rcse
Tg(Wap-cre)11738Mam/0  (conditional)
Gt(ROSA)26Sortm2(myc*T58A)Rcse/Gt(ROSA)26Sortm2(myc*T58A)Rcse
Tg(Wap-cre)11738Mam/0  (conditional)
Gt(ROSA)26Sortm3(myc*S62A)Rcse/Gt(ROSA)26Sortm3(myc*S62A)Rcse
Tg(Wap-cre)11738Mam/0  (conditional)
Myctm2.1Atp/Myctm2.1Atp
Tg(Mx1-cre)1Cgn/0  (conditional)
Myctm2Fwa/Myctm2Fwa
Cd19tm1(cre)Cgn/Cd19+  (conditional)

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