Itgb1em1(IMPC)Bay/Itgb1+
C57BL/6N-Itgb1em1(IMPC)Bay/BayMmucd
|
hyperactivity |
J:211773
|
|
increased startle reflex |
J:211773
|
Itgb1em1(IMPC)Bay/Itgb1em1(IMPC)Bay
C57BL/6N-Itgb1em1(IMPC)Bay/BayMmucd
|
preweaning lethality, complete penetrance |
J:211773
|
Itgb1tm1.1Efu/Itgb1tm1.1Efu
involves: 129X1/SvJ
|
absent inner cell mass |
J:108331
|
|
embryonic lethality between implantation and somite formation, complete penetrance |
J:108331
|
Itgb1tm1Efu/Itgb1tm1Efu
Tg(ATP6V1B1-cre)45Rnel/0
involves: 129X1/SvJ * C57BL/6
|
abnormal kidney cortex morphology |
J:167156
|
|
decreased circulating bicarbonate level |
J:167156
|
|
normal
hearing/vestibular/ear phenotype |
J:167156
|
|
increased urine pH |
J:167156
|
|
metabolic acidosis |
J:167156
|
|
renal tubular acidosis |
J:167156
|
Itgb1tm1Efu/Itgb1tm1Efu
Tg(Cryaa-cre)10Mlr/?
involves: 129X1/SvJ * C57BL/6
|
abnormal lens epithelium morphology |
J:122566
|
|
abnormal lens fiber morphology |
J:122566
|
|
aphakia |
J:122566
|
|
microphthalmia |
J:122566
|
Itgb1tm1Efu/Itgb1tm1Efu
Tg(KRT14-cre)1Efu/0
involves: 129X1/SvJ
|
abnormal basement membrane morphology |
J:65039
|
|
abnormal epidermal layer morphology |
J:65039
|
|
abnormal epidermis stratum basale morphology |
J:65039
|
|
abnormal hair follicle development |
J:65039
|
|
abnormal skin condition |
J:65039
|
|
blistering |
J:65039
|
|
decreased hair follicle number |
J:65039
|
|
dermal-epidermal separation |
J:65039
|
|
neonatal lethality, incomplete penetrance |
J:65039
|
|
thin epidermis |
J:65039
|
|
thin skin |
J:65039
|
Itgb1tm1Efu/Itgb1tm1Efu
Tg(NPHS2-cre)295Lbh/0
involves: 129X1/SvJ * C57BL/6 * SJL
|
abnormal glomerular capillary morphology |
J:135414
|
|
abnormal kidney morphology |
J:135414
|
|
abnormal renal glomerular capsule morphology |
J:135414
|
|
abnormal renal glomerulus basement membrane morphology |
J:135414
|
|
abnormal renal glomerulus morphology |
J:135414
|
|
abnormal renal tubule epithelium morphology |
J:135414
|
|
albuminuria |
J:135414
|
|
decreased body size |
J:135414
|
|
decreased locomotor activity |
J:135414
|
|
dilated glomerular capillary |
J:135414
|
|
dilated renal tubule |
J:135414
|
|
edema |
J:135414
|
|
expanded mesangial matrix |
J:135414
|
|
increased mesangial cell number |
J:135414
|
|
increased podocyte apoptosis |
J:135414
|
|
increased urine protein level |
J:135414
|
|
mesangiolysis |
J:135414
|
|
pale kidney |
J:135414
|
|
podocyte foot process effacement |
J:135414
|
|
premature death |
J:135414
|
|
renal cast |
J:135414
|
|
small kidney |
J:135414
|
Itgb1tm1Efu/Itgb1tm1Efu
Tg(Vil1-cre)997Gum/0
involves: 129X1/SvJ * C57BL/6J * SJL
|
abnormal circulating lipid level |
J:119155
|
|
abnormal crypts of Lieberkuhn morphology |
J:119155
|
|
abnormal enterocyte morphology |
J:119155
|
|
abnormal intestinal absorption |
J:119155
|
|
abnormal intestinal epithelium morphology |
J:119155
|
|
abnormal intestine morphology |
J:119155
|
|
abnormal large intestine morphology |
J:119155
|
|
abnormal small intestine morphology |
J:119155
|
|
decreased body weight |
J:119155
|
|
intestine polyps |
J:119155
|
|
postnatal lethality, complete penetrance |
J:119155
|
|
steatorrhea |
J:119155
|
Itgb1tm1Lscd/Itgb1tm1Lscd
involves: 129X1/SvJ * Black Swiss
|
abnormal blastocoele morphology |
J:28266
|
|
abnormal inner cell mass morphology |
J:28266
|
|
abnormal trophoblast layer morphology |
J:28266
|
|
abnormal visceral endoderm morphology |
J:28266
|
|
embryonic lethality between implantation and somite formation, complete penetrance |
J:28266
|
|
inner cell mass degeneration |
J:28266
|
Itgb1tm1Lscd/Itgb1tm1Mll
Tg(Nes-cre)1Kln/0
involves: 129X1/SvJ * C57BL/6 * SJL
|
abnormal Cajal-Retzius cell morphology |
J:71122
|
|
abnormal cerebellar foliation |
J:71122
|
|
abnormal cerebellum development |
J:71122
|
|
abnormal cerebellum morphology |
J:71122
|
|
abnormal cerebellum vermis morphology |
J:71122
|
|
abnormal cerebral cortex morphology |
J:71122
|
|
abnormal CNS glial cell morphology |
J:71122
|
|
abnormal cortical marginal zone morphology |
J:71122
|
|
abnormal eyelid morphology |
J:71122
|
|
abnormal meninges morphology |
J:71122
|
|
ataxia |
J:71122
|
|
neonatal lethality, complete penetrance |
J:71122
|
|
postnatal growth retardation |
J:71122
|
|
premature death |
J:71122
|
|
small cerebellum |
J:71122
|
Itgb1tm1Lscd/Itgb1tm1Ref
Tg(PLAT-cre)116Sdu/0
involves: 129S1/Sv * 129X1/SvJ
|
abnormal enteric neural crest cell migration |
J:108439
|
|
abnormal enteric neural crest cell morphology |
J:108439
|
|
abnormal enteric neuron morphology |
J:108439
|
|
abnormal innervation |
J:108439
|
|
abnormal neuronal migration |
J:108439
|
|
aganglionic megacolon |
J:108439
|
Itgb1tm1Lscd/Itgb1tm1Ref
Tg(PLAT-cre)116Sdu/0
Not Specified
|
abnormal cranial nerve morphology |
J:92060
|
|
abnormal innervation pattern to muscle |
J:92060
|
|
abnormal motor coordination/balance |
J:92060
|
|
abnormal myelination |
J:92060
|
|
abnormal nervous system morphology |
J:92060
|
|
abnormal neuromuscular synapse morphology |
J:92060
|
|
abnormal sciatic nerve morphology |
J:92060
|
|
absent Schwann cell precursors |
J:92060
|
|
muscular atrophy |
J:92060
|
|
premature death |
J:92060
|
|
progressive muscle weakness |
J:92060
|
Itgb1tm1Mlkn/Itgb1tm1Mlkn
involves: 129/Sv * C57BL/6 * SJL
|
absent inner cell mass |
J:108331
|
|
embryonic lethality between implantation and somite formation, complete penetrance |
J:108331
|
Itgb1tm1Mll/Itgb1tm1Mll
Emx1tm1(cre)Krj/Emx1+
involves: 129S2/SvPas * 129X1/SvJ
|
abnormal Cajal-Retzius cell morphology |
J:170581
|
|
abnormal radial glial cell morphology |
J:170581
|
|
normal
nervous system phenotype |
J:170581
|
|
radial glial endfoot detachment |
J:170581
|
Itgb1tm1Mll/Itgb1tm1Mll
Tg(MMTV-cre)7Mul/0
involves: 129X1/SvJ * FVB/N
|
normal
endocrine/exocrine gland phenotype |
J:92547
|
Itgb1tm1Mll/Itgb1tm1Mll
Tg(Nes-cre)1Kln/0
involves: 129X1/SvJ * C57BL/6 * SJL
|
abnormal neuronal precursor cell migration |
J:120076
|
|
abnormal rostral migratory stream morphology |
J:120076
|
|
small olfactory bulb |
J:120076
|
Itgb1tm1Mll/Itgb1tm1Mll
Tg(Wap-cre)1Gsc/0
involves: 129X1/SvJ * FVB/N
|
abnormal mammary gland growth during lactation |
J:99405
|
|
abnormal mammary gland morphology |
J:99405
|
Itgb1tm1Mll/Itgb1tm1Mll
Wnt3atm1(cre)Eag/Wnt3a+
involves: 129X1/SvJ
|
normal
nervous system phenotype |
J:170581
|
Itgb1tm1Ref/Itgb1tm1Ref
Tg(Col2a1-cre)1Asz/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
|
abnormal bone mineralization |
J:85994
|
|
abnormal bone ossification |
J:85994
|
|
abnormal cartilage development |
J:85994
|
|
abnormal chondrocyte morphology |
J:85994
|
|
abnormal long bone epiphyseal plate morphology |
J:85994
|
|
abnormal long bone hypertrophic chondrocyte zone |
J:85994
|
|
chondrodystrophy |
J:85994
|
|
cleft palate |
J:85994
|
|
decreased body length |
J:85994
|
|
decreased chondrocyte number |
J:85994
|
|
decreased chondrocyte proliferation |
J:85994
|
|
decreased length of long bones |
J:85994
|
|
disproportionate dwarf |
J:85994
|
|
increased chondrocyte apoptosis |
J:85994
|
|
increased diameter of long bones |
J:85994
|
|
neonatal lethality, complete penetrance |
J:85994
|
|
respiratory distress |
J:85994
|
|
short humerus |
J:85994
|
|
short tibia |
J:85994
|
Itgb1tm1Ref/Itgb1tm1Ref
Tg(Ins2-cre)1Heed/?
involves: 129 * C57BL/6 * CBA
|
disorganized pancreatic islets |
J:122649
|
|
increased pancreatic alpha cell number |
J:122649
|
Itgb1tm1Ref/Itgb1tm1Ref
Tg(KRT5-cre)5132Jlj/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2J
|
abnormal dermal layer morphology |
J:65038,
J:148885
|
|
abnormal dermal pigmentation |
J:148885
|
|
abnormal ear position |
J:65038
|
|
abnormal ear shape |
J:65038
|
|
abnormal epidermal-dermal junction morphology |
J:65038,
J:148885
|
|
abnormal epidermis stratum basale morphology |
J:65038
|
|
abnormal esophageal epithelium morphology |
J:65038
|
|
abnormal gait |
J:65038
|
|
abnormal hair follicle morphology |
J:65038,
J:148885,
J:177979
|
|
abnormal hair growth |
J:177979
|
|
abnormal keratinocyte morphology |
J:65038
|
|
absent sebaceous gland |
J:65038
|
|
alopecia |
J:65038
|
|
blistering |
J:65038,
J:148885,
J:177979
|
|
decreased body weight |
J:65038
|
|
decreased hair follicle cell proliferation |
J:65038
|
|
decreased hair follicle number |
J:65038,
J:177979
|
|
epidermal hyperplasia |
J:148885
|
|
hypopigmentation |
J:65038
|
|
impaired skin barrier function |
J:65038
|
|
infertility |
J:148885
|
|
perianal ulcer |
J:65038
|
|
premature death |
J:65038
|
|
progressive hair loss |
J:148885
|
|
reddish skin |
J:65038,
J:177979
|
|
skin inflammation |
J:65038
|
|
skin lesions |
J:65038
|
|
thick epidermis |
J:65038,
J:177979
|
|
tight skin |
J:65038
|
Itgb1tm1Ref/Itgb1tm1Ref
Tg(Mx1-cre)1Cgn/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
|
abnormal platelet physiology |
J:118488
|
|
decreased platelet calcium level |
J:118488
|
Itgb1tm1Ref/Itgb1tm2Ref
Tg(Col2a1-cre)1Asz/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
|
abnormal bone mineralization |
J:85994
|
|
abnormal bone ossification |
J:85994
|
|
abnormal cartilage development |
J:85994
|
|
abnormal chondrocyte morphology |
J:85994
|
|
abnormal long bone epiphyseal plate morphology |
J:85994
|
|
abnormal long bone hypertrophic chondrocyte zone |
J:85994
|
|
chondrodystrophy |
J:85994
|
|
cleft palate |
J:85994
|
|
decreased body length |
J:85994
|
|
decreased chondrocyte number |
J:85994
|
|
decreased chondrocyte proliferation |
J:85994
|
|
decreased length of long bones |
J:85994
|
|
disproportionate dwarf |
J:85994
|
|
increased chondrocyte apoptosis |
J:85994
|
|
increased diameter of long bones |
J:85994
|
|
neonatal lethality, complete penetrance |
J:85994
|
|
respiratory distress |
J:85994
|
|
short humerus |
J:85994
|
|
short tibia |
J:85994
|
Itgb1tm1Ref/Itgb1tm5.1Ref
Tg(KRT5-cre)5132Jlj/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2J
|
abnormal coat/ hair morphology |
J:177979
|
|
abnormal dermal layer morphology |
J:148885
|
|
abnormal dermal pigmentation |
J:148885
|
|
abnormal hair follicle morphology |
J:148885,
J:177979
|
|
abnormal hair follicle outer root sheath morphology |
J:148885
|
|
abnormal hair growth |
J:177979
|
|
blistering |
J:148885
|
|
decreased hair follicle number |
J:177979
|
|
decreased keratinocyte proliferation |
J:148885
|
|
progressive hair loss |
J:148885
|
|
normal
reproductive system phenotype |
J:148885
|
|
sparse hair |
J:148885
|
Itgb1tm1Ref/Itgb1tm12.1Ref
Tg(KRT5-cre)5132Jlj/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2J
|
abnormal hair follicle development |
J:177979
|
|
abnormal hair follicle morphology |
J:177979
|
|
abnormal hair growth |
J:177979
|
|
abnormal skin pigmentation |
J:177979
|
|
alopecia |
J:177979
|
|
blistering |
J:177979
|
|
decreased hair follicle number |
J:177979
|
|
decreased keratinocyte adhesion |
J:177979,
J:203018
|
|
enlarged hair follicles |
J:203018
|
|
reddish skin |
J:177979
|
|
skin lesions |
J:177979
|
|
sparse hair |
J:203018
|
|
thick epidermis |
J:177979
|
Itgb1tm1Ref/Itgb1tm14.1Ref
Tg(KRT5-cre)5132Jlj/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2J
|
abnormal epidermal layer morphology |
J:203018
|
|
abnormal hair growth |
J:203018
|
|
decreased keratinocyte migration |
J:203018
|
|
delayed wound healing |
J:203018
|
|
normal
integument phenotype |
J:203018
|
Itgb1tm1Ref/Itgb1tm15.1Ref
Tg(KRT5-cre)5132Jlj/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2J
|
abnormal epidermal layer morphology |
J:203018
|
|
abnormal hair growth |
J:203018
|
|
decreased keratinocyte adhesion |
J:203018
|
|
decreased keratinocyte proliferation |
J:203018
|
|
enlarged hair follicles |
J:203018
|
Itgb1tm1Ross/Itgb1tm1Ross
Myl2tm1(cre)Krc/Myl2+
involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * Black Swiss
|
abnormal atrial thrombosis |
J:82534
|
|
abnormal cardiac muscle cell glucose uptake |
J:82534
|
|
abnormal cardiac muscle relaxation |
J:82534
|
|
abnormal heart ventricle morphology |
J:82534
|
|
abnormal myocardial fiber morphology |
J:82534
|
|
abnormal myocardium layer morphology |
J:82534
|
|
cardiac fibrosis |
J:82534
|
|
congestive heart failure |
J:82534
|
|
decreased ventricle muscle contractility |
J:82534
|
|
dilated cardiomyopathy |
J:82534
|
|
dilated heart |
J:82534
|
|
dilated heart left ventricle |
J:82534
|
|
dilated heart right ventricle |
J:82534
|
|
increased heart atrium size |
J:82534
|
|
increased response of heart to induced stress |
J:82534
|
|
increased susceptibility to induced morbidity/mortality |
J:82534
|
|
liver vascular congestion |
J:82534
|
|
pleural effusion |
J:82534
|
|
thick ventricular wall |
J:82534
|
Itgb1tm1Ross/Itgb1tm1Ross
Tg(Hoxb7-cre)13Amc/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
|
abnormal kidney collecting duct morphology |
J:149831
|
|
abnormal kidney cortex morphology |
J:149831
|
|
abnormal kidney medulla morphology |
J:149831
|
|
abnormal kidney morphology |
J:149831
|
|
abnormal renal filtration rate |
J:149831
|
|
abnormal renal transport |
J:149831
|
|
abnormal urine homeostasis |
J:149831
|
|
absent kidney |
J:149831
|
|
decreased hematocrit |
J:149831
|
|
decreased kidney weight |
J:149831
|
|
decreased urine osmolality |
J:149831
|
|
dilated kidney collecting duct |
J:149831
|
|
increased blood urea nitrogen level |
J:149831
|
|
increased kidney apoptosis |
J:149831
|
|
increased kidney cell proliferation |
J:149831
|
|
isosthenuria |
J:149831
|
|
kidney failure |
J:149831
|
|
kidney medulla cyst |
J:149831
|
|
kidney medulla hypoplasia |
J:149831
|
|
polyuria |
J:149831
|
|
preweaning lethality, incomplete penetrance |
J:149831
|
|
renal hypoplasia |
J:149831
|
|
single kidney |
J:149831
|
|
small kidney |
J:149831
|
Itgb1tm1Son/Itgb1tm1Son
either: 129P2/OlaHsd-Itgb1tm1Son or (involves: 129P2/OlaHsd * FVB)
|
abnormal cardiovascular system physiology |
J:47279
|
|
normal
muscle phenotype |
J:47279
|
Itgb1tm2Mlkn/Itgb1tm2Mlkn
involves: 129/Sv * C57BL/6 * SJL
|
abnormal platelet physiology |
J:108331
|
Itgb1tm2Son/Itgb1tm2Son
either: 129P2/OlaHsd-Itgb1tm2Son or (involves: 129P2/OlaHsd * FVB)
|
abnormal brain morphology |
J:47279
|
|
abnormal cell adhesion |
J:47279
|
|
abnormal choroid plexus morphology |
J:47279
|
|
abnormal craniofacial morphology |
J:82463
|
|
abnormal digit development |
J:47279
|
|
abnormal eye distance/ position |
J:47279
|
|
abnormal facial morphology |
J:47279
|
|
abnormal first pharyngeal arch morphology |
J:47279
|
|
abnormal head morphology |
J:47279
|
|
abnormal left-right axis patterning |
J:47279
|
|
abnormal limb morphology |
J:47279
|
|
abnormal nervous system morphology |
J:82463
|
|
abnormal neural tube morphology |
J:47279
|
|
anemia |
J:47279
|
|
decreased fibroblast cell migration |
J:47279
|
|
decreased hindbrain size |
J:47279
|
|
embryonic lethality during organogenesis, incomplete penetrance |
J:47279,
J:82463
|
|
hemorrhage |
J:47279,
J:82463
|
|
increased embryonic neuroepithelium thickness |
J:47279
|
|
kinked neural tube |
J:47279
|
|
lethality throughout fetal growth and development, complete penetrance |
J:47279
|
|
mandible hypoplasia |
J:47279
|
|
micrognathia |
J:47279
|
|
small first pharyngeal arch |
J:47279
|
|
small second pharyngeal arch |
J:47279
|
|
spina bifida |
J:47279
|
|
wavy neural tube |
J:47279
|
Itgb1tm2Son/Itgb1tm2Son
FVB.129P2-Itgb1tm2Son
|
abnormal craniofacial morphology |
J:82463
|
|
abnormal head morphology |
J:82463
|
|
abnormal limb morphology |
J:82463
|
|
abnormal myogenesis |
J:82463
|
|
abnormal myotube morphology |
J:82463
|
|
abnormal nervous system morphology |
J:82463
|
|
abnormal pharyngeal arch morphology |
J:82463
|
|
abnormal placenta labyrinth morphology |
J:82463
|
|
abnormal placenta morphology |
J:82463
|
|
abnormal placental labyrinth vasculature morphology |
J:82463
|
|
abnormal posture |
J:82463
|
|
abnormal skeletal muscle morphology |
J:82463
|
|
abnormal spine curvature |
J:82463
|
|
normal
cardiovascular system phenotype |
J:82463
|
|
cyanosis |
J:82463
|
|
decreased body length |
J:82463
|
|
decreased body weight |
J:82463
|
|
decreased fetal size |
J:82463
|
|
decreased skeletal muscle fiber number |
J:82463
|
|
decreased skeletal muscle mass |
J:82463
|
|
embryonic growth arrest |
J:82463
|
|
embryonic lethality during organogenesis, incomplete penetrance |
J:82463
|
|
kinked neural tube |
J:82463
|
|
open neural tube |
J:82463
|
|
pallor |
J:82463
|
|
perinatal lethality, incomplete penetrance |
J:82463
|
Itgb1tm3Mlkn/Itgb1tm3Mlkn
Tg(Mx1-cre)1Cgn/0
involves: 129/Sv * C57BL/6 * CBA
|
decreased circulating noradrenaline level |
J:108331
|
Itgb1tm3Ref/Itgb1tm3Ref
involves: 129S1/Sv * 129X1/SvJ
|
embryonic lethality before implantation, complete penetrance |
J:28330
|
Itgb1tm5.1Ref/Itgb1tm5.1Ref
involves: 129S1/Sv * 129X1/SvJ
|
embryonic lethality between implantation and somite formation, complete penetrance |
J:148885
|
|
preweaning lethality, complete penetrance |
J:177979
|
Itgb1tm6.1Ref/Itgb1tm6.1Ref
involves: 129S1/Sv * 129X1/SvJ
|
no abnormal phenotype detected |
J:177979
|
Itgb1tm7.1Ref/Itgb1tm7.1Ref
involves: 129S1/Sv * 129X1/SvJ
|
no abnormal phenotype detected |
J:177979
|
Itgb1tm8.1Ref/Itgb1tm8.1Ref
involves: 129S1/Sv * 129X1/SvJ
|
no abnormal phenotype detected |
J:177979
|
Itgb1tm9.1Ref/Itgb1tm9.1Ref
involves: 129S1/Sv * 129X1/SvJ
|
normal
integument phenotype |
J:176453
|
|
normal
neoplasm |
J:176453
|
|
no abnormal phenotype detected |
J:177979
|
Itgb1tm9.1Ref/Itgb1tm10.1Ref
involves: 129S1/Sv * 129X1/SvJ
|
normal
integument phenotype |
J:176453
|
|
normal
neoplasm |
J:176453
|
|
no abnormal phenotype detected |
J:177979
|
Itgb1tm10.1Ref/Itgb1tm10.1Ref
involves: 129S1/Sv * 129X1/SvJ
|
abnormal embryo development |
J:185558
|
|
lethality, complete penetrance |
J:185558
|
Itgb1tm11.1Ref/Itgb1tm11.1Ref
involves: 129S1/Sv * 129X1/SvJ
|
decreased incidence of tumors by chemical induction |
J:176453
|
|
decreased keratinocyte adhesion |
J:176453
|
|
normal
integument phenotype |
J:177979
|
Itgb1tm12.1Ref/Itgb1tm12.1Ref
involves: 129S1/Sv * 129X1/SvJ
|
embryonic lethality, complete penetrance |
J:177979
|
Itgb1tm13.1Ref/Itgb1tm13.1Ref
involves: 129S1/Sv * 129X1/SvJ
|
abnormal embryo development |
J:185558
|
|
abnormal embryo implantation |
J:185558
|
|
absent blastocoele |
J:185558
|
|
embryonic lethality, incomplete penetrance |
J:185558
|
|
lethality, complete penetrance |
J:185558
|
Itgb1tm14.1Ref/Itgb1tm14.1Ref
Not Specified
|
abnormal cell physiology |
J:203018
|
|
embryonic lethality, complete penetrance |
J:203018
|
|
lethality, complete penetrance |
J:185558
|
Itgb1tm14.1Ref/Itgb1tm15.1Ref
Not Specified
|
abnormal cell physiology |
J:203018
|
|
embryonic lethality, complete penetrance |
J:203018
|
Itgb1tm15.1Ref/Itgb1tm15.1Ref
Not Specified
|
abnormal cell physiology |
J:203018
|
|
embryonic lethality, complete penetrance |
J:203018
|
Excel File
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