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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Apc
APC, WNT signaling pathway regulator
MGI:88039
231 phenotypes from 25 alleles in 56 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
ApcGt(XA018)Byg/Apc+
(B6.129P2-ApcGt(XA018)Byg x C3H/HeJ)F1
decreased tumor growth/size J:202877
ApcGt(XA018)Byg/Apc+
B6.129P2-ApcGt(XA018)Byg
increased colon adenoma incidence J:202877
increased intestinal adenoma incidence J:202877
increased tumor growth/size J:202877
intestine polyps J:202877
ApcM1Tno/Apc+
either: B6JJcl.B6(D2JJcl)-ApcM1Tno or (involves: C57BL/6 * C57BL/6JJcl * DBA/2JJcl)
increased mammary adenocarcinoma incidence J:218227
increased mammary gland tumor incidence J:218227
increased osteoma incidence J:218227
increased osteosarcoma incidence J:218227
increased pilomatricoma incidence J:218227
increased skin tumor incidence J:218227
increased trichoepithelioma incidence J:218227
premature death J:218227
ApcM1Tno/Apc+
involves: C57BL/6 * DBA/2JJcl
increased mammary gland tumor incidence J:218227
increased osteoma incidence J:218227
increased skin tumor incidence J:218227
premature death J:218227
ApcM1Tno/ApcM1Tno
involves: C57BL/6 * DBA/2JJcl
embryonic lethality during organogenesis, complete penetrance J:218227
ApcMin/Apc+
(AKR/J x C57BL/6J-ApcMin)F1
aneuploidy J:21369
decreased intestinal adenoma incidence J:1879
extended life span J:1879
increased incidence of tumors by chemical induction J:15101
increased intestinal adenocarcinoma incidence J:21369
ApcMin/Apc+
(MA/MyJ x C57BL/6J-ApcMin)F1
decreased intestinal adenoma incidence J:1879
extended life span J:1879
ApcMin/Apc+
B6(AKR)-ApcMin
abnormal pregnancy J:10209
anemia J:10209
increased intestinal adenocarcinoma incidence J:10209
increased intestinal adenoma incidence J:10209
increased mammary gland tumor incidence J:15101
mammary gland hyperplasia J:15101
premature death J:10209
ApcMin/Apc+
B6.Cg-Brca2tm1Mbn ApcMin
abnormal mammary gland development J:67445
abnormal ovarian follicle morphology J:67445
abnormal ovarian folliculogenesis J:67445
abnormal vagina epithelium morphology J:67445
absent corpus luteum J:67445
absent mature ovarian follicles J:67445
absent nipple J:67445
adrenal gland hyperplasia J:67445
decreased body weight J:67445
increased incidence of induced tumors J:67445
increased mammary gland tumor incidence J:67445
ovary atrophy J:67445
normal reproductive system phenotype J:67445
uterus atrophy J:67445
ApcMin/Apc+
C57BL/6J-ApcMin
decreased macrophage cell number J:85142
hepatic steatosis J:86036
increased circulating free fatty acids level J:86036
increased circulating triglyceride level J:86036
increased colon adenoma incidence J:158733, J:160399
increased intestinal adenoma incidence J:1879, J:85142, J:158733, J:241611
increased prostaglandin level J:85142
postnatal growth retardation J:85142
premature death J:1879
ApcMin/Apc+
C57BL/6J-ApcMin/J
abnormal interleukin secretion J:305794
increased colon adenoma incidence J:331404
increased intestinal adenoma incidence J:331404
premature death J:331404
ApcMin/Apc+
involves: 129 * C57BL/6
decreased NK cell number J:156864
decreased splenocyte number J:156864
decreased T cell number J:156864
intestine polyps J:156864
ApcMin/Apc+
involves: 129P2/OlaHsd * C57BL/6
increased intestinal adenoma incidence J:95893
normal neoplasm J:95893
ApcMin/Apc+
involves: AKR/J * C57BL/6J
anemia J:10209
decreased hematocrit J:10209
hyperlipidemia J:10209
increased intestinal adenocarcinoma incidence J:10209
increased intestinal adenoma incidence J:10209
melena J:10209
premature death J:10209
ApcMin/Apc+
involves: C57BL/6 * C57BL/6J
intestine polyps J:134087
premature death J:134087
ApcMin/Apc+
involves: C57BL/6J
abnormal enterocyte proliferation J:118600
abnormal intestinal goblet cell morphology J:118600
abnormal intestinal mucosa morphology J:118600
abnormal large intestine crypts of Lieberkuhn morphology J:118600
abnormal tumor pathology J:268691
anemia J:75393
decreased intestinal adenoma incidence J:268691
decreased tumor growth/size J:268691
increased intestinal adenoma incidence J:75393, J:94108, J:299895
increased mammary adenocarcinoma incidence J:94108
intestinal obstruction J:75393
intestine polyps J:191217
premature death J:75393, J:94108
rectal prolapse J:94108
ApcMin/Apc+
Tg(Rorc-EGFP)1Ebe/?
involves: C57BL/6
abnormal effector T cell morphology J:137020
colon polyps J:137020
enlarged mesenteric lymph nodes J:137020
intestine polyps J:137020
lymph node hyperplasia J:137020
ApcMin/ApcMin
involves: AKR/J * C57BL/6J
abnormal egg cylinder morphology J:27993
abnormal embryo development J:27993
abnormal embryo size J:27993
ApcMin/ApcMin
involves: C57BL/6 * POMOD
abnormal embryo development J:27993
decreased embryo size J:27993
embryonic lethality between implantation and placentation J:27993
embryonic lethality, complete penetrance J:27993
ApcMin/ApcMin
involves: C57BL/6J
abnormal cell physiology J:187862
ApcMin/ApcMin
involves: C57BL/6J * CAST/EiJ
embryonic lethality, complete penetrance J:27993
ApcMin/Apctm1.1Klne
B6.Cg-ApcMin/Apctm1.1Klne
abnormal enterocyte proliferation J:186132
intestine polyps J:186132
ApcMin/Apctm1Tno
involves: 129 * 129S4/SvJae * C57BL/6
abnormal brain development J:156864
absent forebrain J:156864
absent mandible J:156864
absent midbrain J:156864
acrania J:156864
lethality throughout fetal growth and development, incomplete penetrance J:156864
perinatal lethality, complete penetrance J:156864
Apctm1.1Alew/Apc+
B6.129-Apctm1.1Alew
abnormal tumor morphology J:180275
anemia J:180275
gastrointestinal tract polyps J:180057, J:180275
increased adenoma incidence J:180057
increased apoptosis J:180275
increased cell proliferation J:180275
increased intestinal adenoma incidence J:180057, J:180275
premature death J:180275
Apctm1.1Alew/Apctm1.1Alew
B6.129-Apctm1.1Alew
prenatal lethality, complete penetrance J:180057
Apctm1.1Klne/Apctm1.1Klne
B6.129-Apctm1.1Klne
abnormal enterocyte proliferation J:186132
colon polyps J:186132
gastric polyps J:186132
Apctm1.1Rsmi/Apc+
involves: 129P2/OlaHsd
increased gastrointestinal tumor incidence J:149225
Apctm1.1Rsmi/Apc+
involves: 129P2/OlaHsd * C57BL/6 * FVB/N
anemia J:159883
increased desmoid tumor incidence J:159883
increased gastrointestinal tumor incidence J:159883
increased intestinal adenoma incidence J:159883
increased large intestine adenocarcinoma incidence J:159883
increased small intestine adenocarcinoma incidence J:159883
intestinal obstruction J:159883
premature death J:159883
skin cyst J:159883
Apctm1.1Tno/Apc+
involves: 129S4/SvJae * C57BL/6
anemia J:127452
gastrointestinal hemorrhage J:127452
increased intestinal adenoma incidence J:127452
intestinal obstruction J:127452
intestine polyps J:127452
premature death J:127452
Apctm1.1Tno/Apctm1Tno
involves: 129 * 129S4/SvJae * BALB/cJ * C57BL/6
abnormal brain development J:156864
absent forebrain J:156864
absent mandible J:156864
absent midbrain J:156864
acrania J:156864
perinatal lethality, complete penetrance J:156864
Apctm1.1Tyj/Apc+
involves: 129S4/SvJaeSor * C57BL/6
anemia J:160399
increased colon adenoma incidence J:160399
increased intestinal adenoma incidence J:160399
increased tumor growth/size J:160399
premature death J:160399
Apctm1Cip/Apc+
involves: 129P2/OlaHsd * C57BL/6
anemia J:94108
increased colon adenoma incidence J:94108
increased intestinal adenocarcinoma incidence J:94108
increased intestinal adenoma incidence J:94108
increased mammary adenocarcinoma incidence J:94108
premature death J:94108
rectal hemorrhage J:94108
rectal prolapse J:94108
Apctm1Cip/Apctm1Cip
involves: 129P2/OlaHsd * C57BL/6
prenatal lethality, complete penetrance J:94108
Apctm1Kk/Apctm1Kk
Tg(Lck-cre)1Cwi/?
involves: 129S6/SvEvTac * C57BL/6 * DBA/2
abnormal intestinal mucosa morphology J:104334
abnormal T cell differentiation J:100461
arrested T cell differentiation J:100461
increased circulating tumor necrosis factor level J:128606
increased double-negative T cell number J:100461
increased intestinal adenoma incidence J:104334
increased mast cell number J:128606
intestine polyps J:128606
small thymus J:100461
thymus hypoplasia J:100461
Apctm1Mmt/Apc+
involves: 129S2/SvPas * C57BL/6J
increased intestinal adenoma incidence J:25200, J:79668
intestine polyps J:79668
Apctm1Mmt/Apctm1Mmt
involves: 129S2/SvPas * C57BL/6J
embryonic lethality between implantation and somite formation, incomplete penetrance J:25200
Apctm1Rak/Apc+
(C57BL/6J x 129P2/OlaHsd)F1
epidermal cyst J:151494
increased desmoid tumor incidence J:151494
increased gastrointestinal tumor incidence J:151494
increased stomach tumor incidence J:151494
premature death J:151494
Apctm1Rak/Apc+
B6.129P2-Apctm1Rak
colon polyps J:107273
decreased tumor-free survival time J:107273
gastric polyps J:107273
intestine polyps J:107273
Apctm1Rak/Apc+
involves: 129P2/OlaHsd * C57BL/6
increased hepatocellular carcinoma incidence J:20443
increased intestinal adenocarcinoma incidence J:20443
increased intestinal adenoma incidence J:20443
premature death J:20443
rectal hemorrhage J:20443
Apctm1Rak/Apc+
involves: 129P2/OlaHsd * C57BL/6J
increased intestinal adenocarcinoma incidence J:65142
increased stomach tumor incidence J:65142
Apctm1Rak/Apctm1Rak
involves: 129P2/OlaHsd * C57BL/6
embryonic lethality, complete penetrance J:20443
Apctm1Rfo/Apctm1Rfo
B6.129P2-Apctm1Rfo
postnatal lethality, incomplete penetrance J:55416
Apctm1Rfo/Apctm1Rfo
involves: 129P2/OlaHsd
normal cellular phenotype J:116121
Apctm1Rfo/Apctm1Rfo
involves: 129P2/OlaHsd * C57BL/6J
absent male preputial gland J:55416
decreased body size J:55416
normal mortality/aging J:55416
normal neoplasm J:55416
postnatal growth retardation J:55416
skin cyst J:55416
Apctm1Rsmi/Apc+
Tg(Fabp1-cre)1Jig/0
involves: 129P2/OlaHsd * FVB/N
increased gastrointestinal tumor incidence J:159883
increased intestinal adenocarcinoma incidence J:159883
increased intestinal adenoma incidence J:159883
increased large intestine adenocarcinoma incidence J:159883
increased small intestine adenocarcinoma incidence J:159883
increased tumor-free survival time J:159883
Apctm1Rsmi/Apctm1Rsmi
involves: 129P2/OlaHsd
normal neoplasm J:149225
no abnormal phenotype detected J:149225
Apctm1Rsmi/Apctm1Rsmi
Pgrtm2(cre)Lyd/Pgr+
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6J
abnormal internal female genitalia morphology J:210095
abnormal oviduct morphology J:210095
endometrium hyperplasia J:210095
increased granulosa cell tumor incidence J:210095
increased ovary tumor incidence J:210095
increased reproductive system tumor incidence J:210095
ovary cyst J:210095
Apctm1Rsmi/Apctm1Rsmi
Tg(Col2a1-cre)1Rsjo/0
involves: 129P2/OlaHsd * FVB/N
abnormal abdominal wall morphology J:149225
abnormal bone mineralization J:149225
abnormal cartilage development J:149225
abnormal chondrocyte morphology J:149225
abnormal craniofacial morphology J:149225
abnormal cranium morphology J:149225
abnormal endochondral bone ossification J:149225
abnormal forelimb morphology J:149225
abnormal hindlimb morphology J:149225
abnormal humerus morphology J:149225
abnormal limb development J:149225
abnormal mandible morphology J:149225
abnormal rib morphology J:149225
abnormal skeleton development J:149225
abnormal thoracic cavity morphology J:149225
absent sternum J:149225
blistering J:149225
decreased body length J:149225
decreased fetal size J:149225
enhanced osteoblast differentiation J:149225
perinatal lethality, incomplete penetrance J:149225
postnatal lethality, complete penetrance J:149225
scapular bone hypoplasia J:149225
short forelimb J:149225
short hindlimb J:149225
short ribs J:149225
Apctm1Tno/Apc+
involves: 129 * 129S4/SvJae * C57BL/6
increased hepatocellular carcinoma incidence J:156864
Apctm1Tno/Apc+
Tg(Vil1-cre)997Gum/0
involves: 129S4/SvJae * C57BL/6 * SJL
anemia J:126018
increased gastrointestinal tumor incidence J:126018
increased small intestine adenocarcinoma incidence J:126018
postnatal growth retardation J:126018
Apctm1Tno/Apc+
Tg(CDX2-cre)101Erf/0
involves: 129S4/SvJae * C57BL/6 * SJL
anemia J:126018
decreased body weight J:126018
decreased hematocrit J:126018
increased gastrointestinal tumor incidence J:126018
increased mammary adenocarcinoma incidence J:126018
increased tumor incidence J:126018
intestinal obstruction J:126018
premature death J:126018
rectal prolapse J:126018
Apctm1Tno/Apc+
Tg(CDX2-cre*)189Erf/0
involves: 129S4/SvJae * C57BL/6 * SJL
normal neoplasm J:148161
Apctm1Tno/Apc+
Tg(CDX2-cre/ERT)#Erf/0
involves: 129S4/SvJae
increased gastrointestinal tumor incidence J:189226
Apctm1Tno/Apctm1Tno
involves: 129 * 129S4/SvJae * C57BL/6
increased hepatocellular carcinoma incidence J:156864
increased incidence of tumors by chemical induction J:156864
Apctm1Tno/Apctm1Tno
involves: 129S4/SvJae * C57BL/6
increased colon adenoma incidence J:43301
Apctm1Tno/Apctm1Tno
Lgr5tm1(cre/ERT2)Cle/Lgr5+
involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6
increased intestinal adenoma incidence J:227334
Apctm1Tno/Apctm1Tno
Tg(Cdh16-cre)91Igr/0
involves: 129S4/SvJae * ICR
decreased body weight J:95502
enlarged kidney J:95502
increased blood urea nitrogen level J:95502
increased renal cystadenoma incidence J:95502
kidney cyst J:95502
polycystic kidney J:95502
postnatal lethality, incomplete penetrance J:95502
premature death J:95502
Apctm1Tno/Apctm1Tno
Tg(CDX2-cre)101Erf/0
involves: 129S4/SvJae * C57BL/6 * SJL
embryonic lethality, complete penetrance J:126018
Apctm1Tno/Apctm1Tno
Tg(CDX2-cre*)189Erf/0
involves: 129S4/SvJae * C57BL/6 * SJL
increased colon adenoma incidence J:148161
intestine polyps J:148161
kinked tail J:148161
postnatal lethality, complete penetrance J:148161
premature death J:148161
short tail J:148161
Apctm1Tno/Apctm1Tno
Tg(Cyp1a1-cre/ERT)1Dwi/0
involves: 129S4/SvJae * C57BL/6 * CBA
abnormal urinary bladder urothelium morphology J:164579
Apctm1Tno/Apctm1Tno
Tg(Pbsn-cre)4Prb/0
involves: 129S4/SvJae * C57BL/6 * C57BL/6J * DBA/2
increased prostate gland adenocarcinoma incidence J:120308
increased prostate intraepithelial neoplasia incidence J:120308
increased tumor incidence J:120308
premature death J:120308
prostate gland epithelial hyperplasia J:120308
Apctm1Tno/Apctm1Tno
Tg(Vil1-cre)997Gum/0
involves: 129S4/SvJae * C57BL/6 * SJL
embryonic lethality, complete penetrance J:126018
Apctm1Tyj/Apc+
Tg(Vil1-cre)20Syr/0
involves: C57BL/6 * DBA/2
increased colon adenoma incidence J:160399
increased intestinal adenoma incidence J:160399
Apctm1Tyj/Apctm1Tyj
involves: 129P2/OlaHsd * C57BL/6
no abnormal phenotype detected J:159014
Apctm2.1Alew/Apc+
B6.129-Apctm2.1Alew
abnormal tumor pathology J:180057
anemia J:180057
gastrointestinal tract polyps J:180057
hunched posture J:180057
increased adenoma incidence J:180057
increased intestinal adenoma incidence J:180057
Apctm2.1Alew/Apctm2.1Alew
B6.129-Apctm2.1Alew
prenatal lethality, complete penetrance J:180057
Apctm2.1Cip/Apc+
Tg(Fabp1-cre)1Jig/0
involves: 129P2/OlaHsd * FVB/N
increased intestinal adenocarcinoma incidence J:132357
Apctm2.1Cip/Apc+
Tg(Vil1-cre)20Syr/0
involves: 129P2/OlaHsd * C57BL/6 * DBA/2
increased colon adenoma incidence J:160399
increased intestinal adenoma incidence J:160399
Apctm2.1Cip/Apc+
Tg(Vil1-cre/ERT2)23Syr/0
involves: 129P2/OlaHsd * C57BL/6 * DBA/2
abnormal autophagy J:227287
abnormal gut flora balance J:227287
cachexia J:227287
decreased tumor-free survival time J:227287
increased colon adenoma incidence J:227287
increased intestinal adenoma incidence J:227287
intestine polyps J:227287
rectal prolapse J:227287
Apctm2.1Cip/Apc+
Lgr5tm1(cre/ERT2)Cle/Lgr5+
involves: 129P2/OlaHsd * C57BL/6
normal neoplasm J:186084
Apctm2.1Cip/Apc+
Lrig1tm1.1(cre/ERT2)Rjc/Lrig1+
involves: 129 * 129P2/OlaHsd * C57BL/6
increased intestinal adenoma incidence J:186084
Apctm2.1Cip/Apctm2.1Cip
involves: 129P2/OlaHsd * C57BL/6N
increased hepatocellular carcinoma incidence J:94721
liver hyperplasia J:94721
premature death J:94721
Apctm2.1Cip/Apctm2.1Cip
Tg(Ttr-cre/Esr1*)1Vco/0
B6.Cg-Apctm2.1Cip Tg(Ttr-cre/Esr1*)1Vco
abnormal liver morphology J:184496
abnormal NK T cell physiology J:184496
decreased NK T cell number J:184496
enlarged liver J:184496
increased interferon-gamma secretion J:184496
increased interleukin-4 secretion J:184496
liver inflammation J:184496
Apctm2.1Cip/Apctm2.1Cip
Tg(Vil1-cre/ERT2)23Syr/0
involves: 129P2/OlaHsd * C57BL/6 * DBA/2
abnormal colon morphology J:98469
abnormal intestinal epithelium morphology J:98469
abnormal intestinal goblet cell morphology J:98469
abnormal intestine development J:98469
abnormal small intestine crypts of Lieberkuhn morphology J:98469
increased small intestinal crypt cell apoptosis J:98469
premature death J:98469
Apctm2.1Rak/Apc+
involves: 129/Sv * C57BL/6J * SJL
abnormal nursing J:114152
anemia J:114152
increased gastrointestinal tumor incidence J:114152
increased intestinal adenoma incidence J:114152
premature death J:114152
rectal hemorrhage J:114152
Apctm2Mmt/Apc+
involves: 129X1/SvJ
increased intestinal adenoma incidence J:81402
Apctm2Mmt/Apctm2Mmt
involves: 129X1/SvJ
embryonic lethality J:81402
Apctm2Mmt/Apctm3Mmt
involves: 129X1/SvJ * C57BL/6N
abnormal egg cylinder morphology J:81402
abnormal embryonic epiblast morphology J:81402
abnormal embryonic tissue morphology J:81402
Apctm2Rak/Apc+
Tg(Car1-cre)5Flt/0
involves: 129/Sv * C57BL/6J * SJL
anemia J:164247
colon polyps J:164247
decreased hematocrit J:164247
normal homeostasis/metabolism phenotype J:164247
increased incidence of tumors by chemical induction J:164247
increased intestinal adenoma incidence J:164247
melena J:164247
normal neoplasm J:164247
Apctm2Rak/Apctm2.1Rak
involves: 129/Sv * C57BL/6J * SJL
no abnormal phenotype detected J:114152
Apctm2Rak/Apctm2Rak
involves: 129/Sv * C57BL/6J * SJL
increased carcinoma incidence J:156532
increased colon adenoma incidence J:156532
increased organ/body region tumor incidence J:156532
Apctm2Rak/Apctm2Rak
Tg(Car1-cre)5Flt/0
involves: 129/Sv * C57BL/6J * SJL
decreased body weight J:164247
decreased hematocrit J:164247
increased intestinal adenoma incidence J:164247
premature death J:164247
rectal prolapse J:164247
Apctm2Rak/Apctm2Rak
Tg(KRT14-cre)8Brn/0
involves: 129/Sv * C57BL/6J * FVB/N * SJL
abnormal cell proliferation J:114152
abnormal ear shape J:114152
abnormal hair follicle bulb morphology J:114152
abnormal hair follicle development J:114152
abnormal hair follicle morphology J:114152
abnormal hair follicle orientation J:114152
abnormal Hassall's corpuscle morphology J:114152
abnormal keratinocyte differentiation J:114152
abnormal skin pigmentation J:114152
abnormal thymus morphology J:114152
abnormal tooth development J:114152
absent teeth J:114152
absent upper incisors J:114152
blepharoptosis J:114152
cornea epithelium hyperplasia J:114152
decreased body size J:114152
decreased thymocyte number J:114152
delayed hair appearance J:114152
Harderian gland hyperplasia J:114152
increased ear pigmentation J:114152
increased forehead pigmentation J:114152
lethargy J:114152
postnatal lethality, complete penetrance J:114152
salivary gland epithelial hyperplasia J:114152
scaly skin J:114152
short hair J:114152
short vibrissae J:114152
skin ridges J:114152
small stomach J:114152
small thymus J:114152
underdeveloped hair follicles J:114152
weight loss J:114152
wrinkled skin J:114152
Apctm2Rak/Apctm2Rak
Tg(Pdx1-cre)6Tuv/0
involves: 129/Sv * C57BL/6J * FVB/N * SJL
abnormal intestine development J:234310
abnormal pancreas development J:234310
decreased pancreatic beta cell mass J:234310
decreased pancreatic islet number J:234310
duodenal atresia J:234310
neonatal lethality, complete penetrance J:234310
Apctm2Rfo/Apc+
129P2/OlaHsd-Apctm2Rfo
increased gastrointestinal tumor incidence J:151494
increased liver tumor incidence J:151494
increased mammary adenocarcinoma incidence J:151494
premature death J:151494
Apctm2Rfo/Apc+
(C57BL/6J x 129P2/OlaHsd)F1
epidermal cyst J:151494
increased desmoid tumor incidence J:151494
increased liver tumor incidence J:151494
increased mammary adenocarcinoma incidence J:151494, J:204440
increased mammary gland tumor incidence J:151494
increased metastatic potential J:204440
increased tumor incidence J:151494
premature death J:151494
Apctm2Rfo/Apc+
B6.129P2-Apctm2Rfo
increased liver tumor incidence J:151494
increased mammary adenocarcinoma incidence J:151494
increased mammary gland tumor incidence J:151494
premature death J:151494
Apctm2Rfo/Apctm2Rfo
B6.129P2-Apctm2Rfo
postnatal lethality, complete penetrance J:151494
Apctm2Tno/Apc+
involves: C57BL/6J
hepatic steatosis J:86036
hyperlipidemia J:86036
increased circulating cholesterol level J:86036
increased circulating free fatty acids level J:86036
increased circulating triglyceride level J:86036
intestine polyps J:86036
Apctm2Tno/Apc+
Not Specified
increased intestinal adenoma incidence J:47857
premature death J:47857
Apctm3Mmt/Apc+
B6.129X1-Apctm3Mmt
increased intestinal adenoma incidence J:101604
intestine polyps J:101604
Apctm3Mmt/Apc+
involves: 129X1/SvJ * C57BL/6N
intestine polyps J:81402
Apctm3Mmt/Apctm3Mmt
involves: 129X1/SvJ * C57BL/6N
abnormal anterior visceral endoderm morphology J:81402
abnormal brain development J:81402
abnormal developmental patterning J:81402
abnormal endocardial heart tube morphology J:81402
abnormal floor plate morphology J:81402
abnormal foregut morphology J:81402
abnormal head development J:81402
abnormal hindbrain development J:81402
abnormal mesendoderm development J:81402
abnormal neural tube morphology J:81402
abnormal primitive node morphology J:81402
absent forebrain J:81402
absent midbrain J:81402
absent neural folds J:81402
cardia bifida J:81402
embryonic lethality during organogenesis, complete penetrance J:81402
embryonic-extraembryonic boundary constriction J:81402
incomplete embryo turning J:81402
rostral body truncation J:81402
rostral-caudal axis duplication J:81402
split notochord J:81402
Apctm4Mmt/Apc+
B6.129X1-Apctm4Mmt
increased intestinal adenoma incidence J:101604
intestine polyps J:101604
Apctm4Mmt/Apctm4Mmt
B6.129X1-Apctm4Mmt
embryonic lethality during organogenesis, complete penetrance J:101604

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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
11/12/2024
MGI 6.24
The Jackson Laboratory