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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Arhgap35
Rho GTPase activating protein 35
MGI:1929494
45 phenotypes from 3 alleles in 5 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Arhgap35m1Bchd/Arhgap35m1Bchd
involves: C3H/HeNCrl * C57BL/6J
abnormal cilium morphology J:232342
abnormal kidney morphology J:232342
abnormal neural tube closure J:232342
abnormal renal tubule epithelial cell primary cilium morphology J:232342
abnormal S-shaped body morphology J:232342
dilated proximal convoluted tubule J:232342
dilated renal glomerular capsule J:232342
exencephaly J:232342
kidney cortex cyst J:232342
perinatal lethality, incomplete penetrance J:232342
postnatal lethality, complete penetrance J:232342
renal glomerulus cyst J:232342
renal hypoplasia J:232342
single kidney J:232342
spina bifida J:232342
Arhgap35m1Bchd/Arhgap35tm1Jset
involves: 129S2/SvPas * C3H/HeNCrl * C57BL/6J
abnormal kidney morphology J:232342
abnormal neural tube closure J:232342
exencephaly J:232342
perinatal lethality, complete penetrance J:232342
renal glomerulus cyst J:232342
renal hypoplasia J:232342
single kidney J:232342
spina bifida J:232342
Arhgap35tm1Jset/Arhgap35tm1Jset
involves: 129S2/SvPas
abnormal kidney morphology J:232342
abnormal neural tube closure J:232342
exencephaly J:232342
perinatal lethality, complete penetrance J:232342
renal glomerulus cyst J:232342
renal hypoplasia J:232342
single kidney J:232342
spina bifida J:232342
Arhgap35tm1Jset/Arhgap35tm1Jset
involves: 129S2/SvPas * C57BL/6J
abnormal anterior commissure pars posterior morphology J:68904
abnormal brain commissure morphology J:65296
abnormal cranial nerve morphology J:68904
abnormal facial nerve morphology J:68904
abnormal floor plate morphology J:65296
abnormal glossopharyngeal nerve morphology J:68904
abnormal hypoglossal nerve morphology J:68904
abnormal innervation J:68904
abnormal optic fissure closure J:65296
abnormal roof plate morphology J:65296
abnormal stratification in cerebral cortex J:65296, J:68904
abnormal third ventricle morphology J:65296
abnormal trigeminal nerve morphology J:68904
abnormal vagus ganglion morphology J:68904
absent anterior commissure J:65296
absent corpus callosum J:65296
absent hippocampal commissure J:65296
coloboma J:65296
decreased body size J:65296
decreased embryo size J:65296
exencephaly J:65296
incomplete rostral neuropore closure J:65296
microphthalmia J:65296
omphalocele J:65296
postnatal lethality, complete penetrance J:65296
retina fold J:65296
retina pigment epithelium hyperplasia J:65296
Arhgap35tm2Jset/Arhgap35tm2Jset
involves: 129S2/SvPas * C57BL/6
abnormal embryo development J:160127
abnormal eye morphology J:160127
abnormal kidney morphology J:160127
abnormal nervous system development J:160127
perinatal lethality J:160127

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