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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Itgav
integrin alpha V
MGI:96608
75 phenotypes from 3 alleles in 8 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Itgavtm1Hyn/Itgavtm1Hyn
either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6J)
abnormal blood vessel morphology J:50951
abnormal craniofacial development J:50951
abnormal embryonic growth/weight/body size J:50951
abnormal extraembryonic tissue morphology J:50951
abnormal heart morphology J:50951
abnormal placenta morphology J:50951
abnormal placenta vasculature J:50951
abnormal secondary palate development J:50951
abnormal trophoblast layer morphology J:50951
abnormal vitelline vasculature morphology J:50951
cleft secondary palate J:50951
decreased placental labyrinth size J:50951
embryonic growth retardation J:50951
embryonic lethality during organogenesis, incomplete penetrance J:50951
enlarged heart J:50951
hemorrhage J:50951
hydrocephaly J:50951
intestinal hemorrhage J:50951
intracerebral hemorrhage J:50951
microcephaly J:50951
neonatal lethality, complete penetrance J:50951
palatal shelves fail to meet at midline J:50951
pericardial edema J:50951
small pharyngeal arch J:50951
thin myocardium J:50951
trabecula carnea hypoplasia J:50951
Itgavtm1Hyn/Itgavtm1Hyn
involves: 129S2/SvPas * C57BL/6 * FVB/N
abnormal blood vessel morphology J:79611
embryonic lethality during organogenesis, incomplete penetrance J:79611
intracerebral hemorrhage J:79611
neonatal lethality, complete penetrance J:79611
Itgavtm2.1Hyn/Itgavtm2.1Hyn
involves: 129P2/OlaHsd
intracerebral hemorrhage J:94376
Itgavtm2Hyn/Itgavtm2.1Hyn
Cd19tm1(cre)Cgn/Cd19+
involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * FVB
normal digestive/alimentary phenotype J:125508
Itgavtm2Hyn/Itgavtm2.1Hyn
Lyz2tm1(cre)Ifo/Lyz2+
involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * FVB
colitis J:125508
impaired macrophage phagocytosis J:125508
increased autoantibody level J:125508
Itgavtm2Hyn/Itgavtm2.1Hyn
Tg(GFAP-cre)#Gtm/0
involves: 129P2/OlaHsd * C57BL/6 * CBA
cerebellum hemorrhage J:94376
intracerebral hemorrhage J:94376
intracranial hemorrhage J:94376
Itgavtm2Hyn/Itgavtm2.1Hyn
Tg(Nes-cre)1Kln/0
involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 * FVB * SJL
abnormal brain vasculature morphology J:94376
abnormal embryonic/fetal subventricular zone morphology J:94376
abnormal gait J:94376
abnormal glial cell morphology J:94376
abnormal involuntary movement J:94376
abnormal motor capabilities/coordination/movement J:94376
abnormal posture J:94376
abnormal renal/urinary system physiology J:94376
ataxia J:94376
axon degeneration J:94376
axonal dystrophy J:94376
convulsive seizures J:94376
demyelination J:94376
gliosis J:94376
impaired coordination J:94376
impaired limb coordination J:94376
increased susceptibility to bacterial infection induced morbidity/mortality J:94376
intracerebral hemorrhage J:94376
intracranial hemorrhage J:94376
muscle hypertonia J:94376
normal muscle phenotype J:94376
normal nervous system phenotype J:94376
paraparesis J:94376
premature death J:94376
seizures J:94376
spinal hemorrhage J:94376
Itgavtm2Hyn/Itgavtm2.1Hyn
Tg(Tek-cre)1Ywa/0
involves: 129P2/OlaHsd * C57BL/6 * SJL
normal cardiovascular system phenotype J:94376
Itgavtm2Hyn/Itgavtm2.1Hyn
Tg(Tek-cre)1Ywa/?
involves: 129S2/SvPas * C57BL/6 * FVB * SJL
abnormal dendritic cell differentiation J:125508
abnormal immune system morphology J:125508
abnormal immune system physiology J:125508
abnormal interferon level J:125508
abnormal interleukin level J:125508
abnormal intestinal epithelium morphology J:125508
abnormal leukocyte morphology J:125508
abnormal tumor necrosis factor level J:125508
colitis J:125508
crypts of Lieberkuhn abscesses J:125508
decreased regulatory T cell number J:125508
enlarged mesenteric lymph nodes J:125508
enlarged Peyer's patches J:125508
impaired macrophage phagocytosis J:125508
increased autoantibody level J:125508
increased inflammatory response J:125508
increased intestinal adenocarcinoma incidence J:125508
increased regulatory T cell number J:125508
intestinal ulcer J:125508
large intestinal inflammation J:125508
premature death J:125508
weight loss J:125508

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
04/23/2024
MGI 6.23
The Jackson Laboratory