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
|