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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Myc
myelocytomatosis oncogene
MGI:97250
199 phenotypes from 42 alleles in 39 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
Gt(ROSA)26Sortm1(Myc)Rcse/Gt(ROSA)26Sortm1(Myc)Rcse
Tg(Wap-cre)11738Mam/0
involves: 129 * C57BL/6 * SJL 		abnormal branching of the mammary ductal tree J:169403
abnormal chromosome number J:169403
abnormal mammary gland epithelium physiology J:169403
chromosomal instability J:169403
increased mammary gland apoptosis J:169403
normal neoplasm J:169403
Gt(ROSA)26Sortm2(myc*T58A)Rcse/Gt(ROSA)26Sortm2(myc*T58A)Rcse
Tg(Wap-cre)11738Mam/0
involves: 129 * C57BL/6 * SJL 		abnormal branching of the mammary ductal tree J:169403
abnormal involution of the mammary gland J:169403
abnormal mammary gland alveolus morphology J:169403
abnormal mammary gland epithelium physiology J:169403
aneuploidy J:169403
chromosomal instability J:169403
decreased tumor-free survival time J:169403
increased brain tumor incidence J:169403
increased mammary adenocarcinoma incidence J:169403
increased pituitary gland tumor incidence J:169403
mammary gland alveolar hyperplasia J:169403
mammary gland hyperplasia J:169403
polyploidy J:169403
Gt(ROSA)26Sortm3(myc*S62A)Rcse/Gt(ROSA)26Sortm3(myc*S62A)Rcse
Tg(Wap-cre)11738Mam/0
involves: 129 * C57BL/6 * SJL 		abnormal branching of the mammary ductal tree J:169403
abnormal mammary gland alveolus morphology J:169403
aneuploidy J:169403
chromosomal instability J:169403
increased brain tumor incidence J:169403
polyploidy J:169403
Hnf4atm1(cre)Sdv/Hnf4a+
Myctm2.1Atp/Myctm2.1Atp
involves: 129P2/OlaHsd * 129S/SvEv 		normal liver/biliary system phenotype J:137630
normal mortality/aging J:137630
Mycem1(IMPC)Kmpc/Myc+
C57BL/6NTac-Mycem1(IMPC)Kmpc/Kmpc 		abnormal bone structure J:211773
decreased body length J:211773
decreased bone mineral content J:211773
decreased bone mineral density J:211773
decreased fluid intake J:211773
decreased prepulse inhibition J:211773
increased startle reflex J:211773
increased total body fat amount J:211773
short tibia J:211773
Mycem1(IMPC)Kmpc/Mycem1(IMPC)Kmpc
C57BL/6NTac-Mycem1(IMPC)Kmpc/Kmpc 		preweaning lethality, complete penetrance J:211773
Myctm1(Nmyc1)Fwa/Myctm1(Nmyc1)Fwa
involves: 129P2/OlaHsd * C57BL/6 		prenatal lethality, complete penetrance J:62573
Myctm1.1(MYC)Gwbk/Myctm1.1(MYC)Gwbk
involves: BALB/cJ * C57BL/6 		no abnormal phenotype detected J:189677
Myctm1.1(Nmyc1)Fwa/Myctm1.1(Nmyc1)Fwa
involves: 129P2/OlaHsd * C57BL/6 		abnormal skeletal muscle morphology J:62573
cyanosis J:62573
decreased birth body size J:62573
decreased birth weight J:62573
decreased body size J:62573
decreased body weight J:62573
normal immune system phenotype J:62573
neonatal lethality, incomplete penetrance J:62573
Myctm1.1Cksn/Myctm1.1Cksn
B6.129-Myctm1.1Cksn 		normal immune system phenotype J:170508
Myctm1.1Dlev/Myctm1.1Dlev
involves: 129S4/SvJae * C57BL/6NCrl 		no abnormal phenotype detected J:186832
Myctm1.1Dmlo/Myctm1.1Dmlo
involves: 129S2/SvPas * BALB/c * C57BL/6J * MF1 		no abnormal phenotype detected J:70610
Myctm1.1Itl/Myctm1.1Itl
involves: 129S6/SvEvTac * C57BL/6NTac 		abnormal enterocyte physiology J:188927
abnormal enterocyte proliferation J:188927
abnormal intestinal enteroendocrine cell morphology J:188927
abnormal intestinal goblet cell morphology J:188927
abnormal intestine morphology J:188927
abnormal large intestine crypts of Lieberkuhn morphology J:188927
abnormal response to injury J:188927
abnormal small intestine crypts of Lieberkuhn morphology J:188927
decreased Paneth cell number J:188927
decreased small intestinal villus size J:188927
Myctm1Atp/Myc+
B6.129P2-Myctm1Atp 		abnormal NK cell physiology J:132730
decreased memory T cell number J:132730
decreased T cell proliferation J:132730
normal immune system phenotype J:132730
Myctm1Atp/Myc+
involves: 129P2/OlaHsd * FVB/N 		decreased body size J:73369
decreased body weight J:73369
decreased bone marrow cell number J:73369
decreased fetal size J:73369
decreased fibroblast proliferation J:73369
decreased T cell proliferation J:73369
decreased white adipose tissue amount J:73369
lymph node hypoplasia J:73369
lymphoid hypoplasia J:73369
postnatal growth retardation J:73369
short tail J:73369
small lymphoid organs J:73369
spleen hypoplasia J:73369
Myctm1Atp/Myctm1Atp
involves: 129P2/OlaHsd 		abnormal chorion morphology J:137630
abnormal placenta morphology J:137630
abnormal trophoblast layer morphology J:137630
normal cardiovascular system phenotype J:137630
placental labyrinth hypoplasia J:137630
Myctm1Atp/Myctm1Atp
involves: 129P2/OlaHsd * FVB/N 		absent common myeloid progenitor cells J:73369
absent erythroid progenitor cell J:73369
absent fibroblast proliferation J:73369
decreased embryo size J:73369
embryonic lethality during organogenesis, complete penetrance J:73369
pale yolk sac J:73369
Myctm1Atp/Myctm2.1Atp
involves: 129P2/OlaHsd * C57BL/6 * FVB/N * SJL 		decreased body weight J:73369
decreased bone marrow cell number J:73369
decreased T cell proliferation J:73369
normal immune system phenotype J:73369
lymph node hypoplasia J:73369
spleen hypoplasia J:73369
Myctm1Atp/Myctm2.1Atp
Tg(Mx1-cre)1Cgn/0
involves: 129P2/OlaHsd * C57BL/6 * CBA * FVB/N * SJL 		normal immune system phenotype J:73369
Myctm1Brd/Myc+
involves: 129S7/SvEvBrd * C57BL/6J 		decreased litter size J:4556
reduced female fertility J:4556
Myctm1Brd/Myctm1Brd
involves: 129S7/SvEvBrd * C57BL/6J 		abnormal embryo turning J:4556
distended pericardium J:4556
embryonic growth retardation J:4556
embryonic lethality during organogenesis, complete penetrance J:4556
enlarged heart J:4556
open neural tube J:4556
Myctm1Jlc/Myctm1Jlc
involves: 129S7/SvEvBrd 		abnormal angiogenesis J:79427
abnormal dorsal aorta morphology J:79427
abnormal embryonic erythropoiesis J:79427
abnormal vascular development J:79427
abnormal vasculogenesis J:79427
abnormal visceral yolk sac morphology J:79427
decreased cell proliferation J:79427
decreased common myeloid progenitor cell number J:79427
decreased embryo size J:79427
decreased erythroid progenitor cell number J:79427
decreased tumor incidence J:79427
Myctm1Lbox/Myc+
involves: 129S1/Sv * 129X1/SvJ * FVB/N 		enlarged lymph nodes J:97900
enlarged spleen J:97900
increased B cell derived lymphoma incidence J:97900
increased B cell number J:97900
increased spleen weight J:97900
premature death J:97900
Myctm1Lbox/Myctm1Lbox
involves: 129S1/Sv * 129X1/SvJ * FVB/N 		decreased T cell number J:97900
enlarged lymph nodes J:97900
enlarged spleen J:97900
increased B cell apoptosis J:97900
increased B cell derived lymphoma incidence J:97900
increased B cell number J:97900
increased B cell proliferation J:97900
increased spleen weight J:97900
premature death J:97900
Myctm1Slek/Myctm1Slek
involves: 129 		no abnormal phenotype detected J:131281
Myctm2.1Atp/Myc+
involves: 129P2/OlaHsd * C57BL/6 * SJL 		decreased body weight J:73369
decreased T cell proliferation J:73369
Myctm2.1Atp/Myctm2.1Atp
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129P2/OlaHsd * C57BL/6 * CBA 		abnormal common myeloid progenitor cell morphology J:137630
abnormal proerythroblast morphology J:137630
normal cardiovascular system phenotype J:137630
decreased embryo size J:137630
decreased erythroid progenitor cell number J:137630
embryonic lethality during organogenesis, complete penetrance J:137630
impaired hematopoiesis J:137630
liver hypoplasia J:137630
pale yolk sac J:137630
Myctm2.1Atp/Myctm2.1Atp
Tg(Mx1-cre)1Cgn/0
involves: 129P2/OlaHsd * C57BL/6 * CBA * FVB/N * SJL 		absent fibroblast proliferation J:73369
normal immune system phenotype J:73369
Myctm2.1Atp/Myctm2.1Atp
Tg(Pdx1-cre)1Herr/0
involves: 129P2/OlaHsd * C57BL/6J * CBA/J 		abnormal enzyme/coenzyme activity J:146087
abnormal pancreas development J:146087
abnormal pancreas morphology J:146087
abnormal pancreas size J:146087
abnormal pancreatic acinar cell morphology J:146087
abnormal pancreatic acinus morphology J:146087
abnormal pancreatic duct morphology J:146087
absent pancreatic acinar cells J:146087
decreased pancreas weight J:146087
normal endocrine/exocrine gland phenotype J:146087
pancreas hypoplasia J:146087
Myctm2.1Atp/Myctm2.1Atp
Tg(Tek-cre)1Rwng/0
involves: 129P2/OlaHsd * FVB/N 		abnormal hematopoietic system morphology/development J:137630
abnormal liver morphology J:137630
normal cardiovascular system phenotype J:137630
embryonic lethality during organogenesis, complete penetrance J:137630
liver hypoplasia J:137630
pale yolk sac J:137630
small liver J:137630
Myctm2Dmlo/Myctm2Dmlo
involves: 129S2/SvPas * BALB/c * C57BL/6J * MF1 		no abnormal phenotype detected J:70610
Myctm2Fwa/Myc+
H2az2Tg(Wnt1-cre)11Rth/H2az2+
involves: 129S6/SvEvTac * C57BL/6 * CBA 		belly spot J:121871
Myctm2Fwa/Myctm2Fwa
involves: 129S6/SvEvTac 		no abnormal phenotype detected J:67222
Myctm2Fwa/Myctm2Fwa
Cd19tm1(cre)Cgn/Cd19+
involves: 129P2/OlaHsd * 129S6/SvEvTac 		decreased B cell proliferation J:67222
Myctm2Fwa/Myctm2Fwa
H2az2Tg(Wnt1-cre)11Rth/H2az2+
involves: 129S6/SvEvTac * C57BL/6 * CBA 		abnormal auditory brainstem response J:121871
abnormal frontal bone morphology J:121871
abnormal malleus morphology J:121871
abnormal middle ear ossicle morphology J:121871
abnormal parietal bone morphology J:121871
absent pinna reflex J:121871
conductive hearing impairment J:121871
decreased body size J:121871
decreased body weight J:121871
short malleus manubrium J:121871
short nasal bone J:121871
short snout J:121871
small cranium J:121871
small malleus J:121871
small nasal bone J:121871
variable body spotting J:121871
Myctm3(Tcrb)Fwa/Myc+
involves: 129 		abnormal T cell receptor beta chain V(D)J recombination J:131995
Myctm4.1Fwa/Myctm4.1Fwa
involves: 129S6/SvEvTac 		induced chromosome breakage J:150339
Myctm37Mnz/Myc+
involves: C57BL/6 		induced chromosome breakage J:145691
Myctm39Mnz/Myc+
involves: C57BL/6 		spontaneous chromosome breakage J:145691
Tg(Alb1-Myc)#Sst/0
involves: C57BL/6 * CBA 		abnormal hepatocyte morphology J:34434
increased hepatocellular carcinoma incidence J:34434
increased liver adenoma incidence J:34434
increased liver weight J:34434
Tg(Ela1-Myc)158Bri/0
involves: C57BL/6 * SJL 		exocrine pancreas atrophy J:76992
increased metastatic potential J:76992
increased pancreas tumor incidence J:76992
increased pancreatic acinar cell carcinoma incidence J:76992
jaundice J:76992
premature death J:76992
small pancreas J:76992
Tg(Ela1-Myc)159Bri/0
involves: C57BL/6 * SJL 		exocrine pancreas atrophy J:76992
increased metastatic potential J:76992
increased pancreas tumor incidence J:76992
increased pancreatic acinar cell carcinoma incidence J:76992
jaundice J:76992
premature death J:76992
small pancreas J:76992
Tg(Ela1-Myc)160Bri/0
involves: C57BL/6 * SJL 		exocrine pancreas atrophy J:76992
increased metastatic potential J:76992
increased pancreas tumor incidence J:76992
increased pancreatic acinar cell carcinoma incidence J:76992
jaundice J:76992
premature death J:76992
small pancreas J:76992
Tg(HBB-Myc)#Cos/0
involves: C57BL/6J * CBA/J 		abnormal immune system organ morphology J:276641
anemia J:276641
normal cardiovascular system phenotype J:276641
decreased body size J:276641
decreased hematocrit J:276641
enlarged kidney J:276641
glomerulosclerosis J:276641
hyperventilation J:276641
increased adenoma incidence J:276641
increased blood urea nitrogen level J:276641
increased circulating creatinine level J:276641
kidney failure J:276641
kidney inflammation J:276641
lethargy J:276641
muscular atrophy J:276641
polycystic kidney J:276641
premature death J:276641
renal interstitial fibrosis J:276641
Tg(HBVX*,-Myc)#Skp/0
Not Specified 		increased hepatocellular carcinoma incidence J:81098
Tg(HBVX*,-Myc)#Skp/Tg(HBVX*,-Myc)#Skp
Not Specified 		abnormal cell nucleus morphology J:202732
abnormal definitive hematopoiesis J:81098
abnormal hepatocyte mitochondrial morphology J:202732
abnormal hepatocyte morphology J:81098
abnormal liver lobule morphology J:81098
abnormal liver morphology J:81098
abnormal liver sinusoid morphology J:81098
decreased liver glycogen level J:81098
enlarged liver J:81098
focal hepatic necrosis J:81098
increased hepatocellular carcinoma incidence J:81098
increased liver iron level J:81098
increased liver weight J:81098
increased macrophage cell number J:81098
liver vascular congestion J:81098
microvesicular hepatic steatosis J:81098
Tg(IghMyc)22Bri/0
B6.Cg-Tg(IghMyc)22Bri/J 		enlarged lymph nodes J:164200
increased lymphoma incidence J:164200
premature death J:164200
spleen hyperplasia J:164200
Tg(IghMyc)22Bri/?
involves: C57BL * C57BL/6 * SJL 		enlarged spleen J:121564
increased lymphocyte cell number J:121564
increased lymphoma incidence J:121564
increased metastatic potential J:121564
premature death J:121564
Tg(IghMyc)22Bri/0
involves: C57BL * C57BL/6 * SJL 		increased lymphoma incidence J:117023
premature death J:117023
Tg(IghMyc)22Bri/0
involves: C57BL/6 * SJL 		abnormal lymphopoiesis J:78177
enlarged lymph nodes J:78177
enlarged spleen J:78177
enlarged thymus J:78177
increased B cell derived lymphoma incidence J:78177, J:186117
increased leukemia incidence J:78177
increased leukocyte cell number J:186117
increased lymphoma incidence J:78177, J:223213
increased pre-B cell number J:223213
increased sarcoma incidence J:78177
increased tumor incidence J:78177
premature death J:78177, J:186117, J:223213
Tg(IghMyc)22Bri/0
involves: C57BL/6N * SJL 		increased B cell apoptosis J:214383
increased lymphoma incidence J:214383
premature death J:214383
Tg(IghMyc)186Brn/0
involves: C57BL/LiA * CBA/BrA 		abnormal cell cycle J:142390
abnormal intracellular organelle morphology J:142390
abnormal mitosis J:142390
binucleate J:142390
Tg(MMTV-Myc)141-3Led/0
involves: C57BL/6J * CD-1 		increased B cell derived lymphoma incidence J:62465
increased Leydig cell number J:62465
increased tumor incidence J:62465
Tg(MMTV-Myc)WT13Jrn/0
involves: FVB/N 		abnormal mammary gland development J:193362
increased mammary adenocarcinoma incidence J:153233
increased mammary gland tumor incidence J:153233, J:193362
increased metastatic potential J:153233
Tg(MMTV-Myc)WT21Jrn/0
involves: FVB/N 		increased mammary adenocarcinoma incidence J:153233
increased mammary gland tumor incidence J:153233, J:193362
increased metastatic potential J:153233
Tg(MMTV-Myc*T58A)TA14Jrn/0
involves: FVB/N 		abnormal mammary gland development J:193362
increased mammary adenocarcinoma incidence J:153233
increased mammary gland tumor incidence J:153233, J:193362
Tg(MMTV-Myc*T58A)TA39Jrn/0
involves: FVB 		increased mammary gland tumor incidence J:193362
Tg(MMTV-Myc*T58A)TA41Jrn/0
involves: FVB/N 		increased mammary adenocarcinoma incidence J:153233
increased mammary gland tumor incidence J:153233, J:193362
Tg(Pklr-Myc)73Ak/0
B6.Cg-Tg(Pklr-Myc)73Ak 		decreased NK T cell number J:184496
increased hepatocellular carcinoma incidence J:184496
Tg(Pklr-Myc)73Ak/0
involves: C57BL/6 * DBA 		increased hepatocellular carcinoma incidence J:185488
increased hepatoma incidence J:185488
pancreatic islet hyperplasia J:185488
Tg(Thy1-cmyc)1Kio/0
Not Specified 		postnatal lethality, complete penetrance J:129440
Tg(Thy1-cmyc)6Kio/0
Not Specified 		increased T cell derived lymphoma incidence J:129440
respiratory distress J:129440
Tg(Thy1-cmyc)6LKio/0
Not Specified 		increased T cell derived lymphoma incidence J:129440
Tg(WapMyc)212Bri/0
FVB.Cg-Tg(WapMyc)212Bri 		abnormal mammary gland lobule morphology J:114568
abnormal mammary gland morphology J:114568
increased mammary gland tumor incidence J:114568
mammary gland duct hyperplasia J:114568
mammary gland hyperplasia J:114568
Tg(WapMyc)212Bri/0
involves: C57BL/6 * SJL 		increased mammary adenocarcinoma incidence J:56318
increased mammary gland tumor incidence J:56318
lactation failure J:56318
mammary gland alveolar hyperplasia J:56318
premature death J:56318
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Send questions and comments to User Support. 		last database update
12/17/2024
MGI 6.24 		The Jackson Laboratory