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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Atmin
ATM interactor
MGI:2682328
65 phenotypes from 6 alleles in 10 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
Atmingpg6/Atmingpg6
C3H.C-Atmingpg6 		abnormal cardiac outflow tract development J:217609
abnormal embryonic neuroepithelium primary cilium morphology J:217609
abnormal primary cilium morphology J:217609
normal cardiovascular system phenotype J:217609
coloboma J:217609
decreased embryonic cilium length J:217609
normal digestive/alimentary phenotype J:217609
edema J:217609
exencephaly J:217609
interrupted aortic arch J:217609
left pulmonary isomerism J:217609
microphthalmia J:217609
small lung J:217609
thick upper lip J:217609
Atmingpg6/Atmingpg6
involves: BALB/cAnN * C3H/HeH 		abnormal craniofacial morphology J:145068
abnormal eye morphology J:145068
abnormal kidney epithelium morphology J:211696
abnormal motile primary cilium morphology J:145068
abnormal truncus arteriosus septation J:145068
absent lungs J:145068
edema J:145068
exencephaly J:145068
impaired branching involved in ureteric bud morphogenesis J:211696
interrupted aortic arch J:145068
left pulmonary isomerism J:145068
micrognathia J:145068
right aortic arch J:145068
right pulmonary isomerism J:145068
situs inversus J:145068
small kidney J:211696
spina bifida J:145068
Atmingpg6/Atminm1H
C3.C-Atmingpg6/Atminm1H 		absent lungs J:217609
normal cardiovascular system phenotype J:217609
coloboma J:217609
normal digestive/alimentary phenotype J:217609
edema J:217609
exencephaly J:217609
left pulmonary isomerism J:217609
microphthalmia J:217609
small lung J:217609
thick upper lip J:217609
Atminm1H/Atminm1H
C3H.C-Atminm1H 		absent lungs J:217609
normal cardiovascular system phenotype J:217609
coloboma J:217609
normal digestive/alimentary phenotype J:217609
edema J:217609
exencephaly J:217609
left pulmonary isomerism J:217609
microphthalmia J:217609
small lung J:217609
thick upper lip J:217609
Atmintm1.1Axbe/Atmintm1.1Axbe
involves: BALB/c * C57BL/6 		abnormal cell physiology J:167331
abnormal craniofacial morphology J:167331
decreased cell proliferation J:167331
early cellular replicative senescence J:167331
exencephaly J:167331
lethality throughout fetal growth and development, complete penetrance J:167331
Atmintm1.1Jhh/Atmintm1.1Jhh
C57BL/6-Atmintm1.1Jhh 		abnormal base-excision repair J:167544
abnormal heart position or orientation J:167544
abnormal respiratory system development J:167544
abnormal trachea development J:167544
absent lungs J:167544
absent trachea J:167544
normal cellular phenotype J:167544
decreased fetal weight J:167544
early cellular replicative senescence J:167544
exencephaly J:167544
fetal growth retardation J:167544
increased cellular sensitivity to hydrogen peroxide J:167544
increased cellular sensitivity to methylmethanesulfonate J:167544
lethality throughout fetal growth and development, complete penetrance J:167544
thymus hypoplasia J:167544
Atmintm1.1Jhh/Atmintm1.1Jhh
Cd79atm1(cre)Reth/Cd79a+
B6.Cg-Cd79atm1(Cre)Reth Atmintm1.1Jhh 		decreased B cell number J:230105
decreased IgG1 level J:230105
decreased immature B cell number J:230105
increased B cell apoptosis J:230105
Atmintm1.1Jhh/Atmintm1.1Jhh
Tg(Fcer2a-cre)5Mbu/0
B6.Cg-Atmintm1.1Jhh Tg(Fcer2a-cre)5Mbu 		normal hematopoietic system phenotype J:230105
normal neoplasm J:230105
Atmintm1.2Jhh/Atmintm1.2Jhh
Cd79atm1(cre)Reth/Cd79a+
involves: BALB/c * C57BL/6 		abnormal B cell differentiation J:191832
abnormal B cell physiology J:191832
decreased immature B cell number J:191832
decreased mature B cell number J:191832
decreased pre-B cell number J:191832
decreased spleen weight J:191832
small spleen J:191832
Atmintm1.2Jhh/Atmintm1.2Jhh
Tg(Mx1-cre)1Cgn/0
involves: C57BL/6 * CBA 		decreased B cell number J:191832
decreased erythrocyte cell number J:191832
decreased lymphocyte cell number J:191832
decreased mature B cell number J:191832
decreased pre-B cell number J:191832
normal immune system phenotype J:191832
Atmintm1Axbe/Atmintm1Axbe
Tg(Nes-cre)1Kln/0
involves: C57BL/6 * SJL 		astrocytosis J:167331
decreased body weight J:167331
decreased neuron number J:167331
hyperactivity J:167331
increased anxiety-related response J:167331
loss of dopaminergic neurons J:167331
neurodegeneration J:167331
premature death J:167331
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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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Send questions and comments to User Support. 		last database update
12/17/2024
MGI 6.24 		The Jackson Laboratory