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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Arhgap33
Rho GTPase activating protein 33
MGI:2673998
13 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Arhgap33tm1.1Wbm/Arhgap33tm1.1Wbm
Not Specified
abnormal auditory cortex morphology J:185948
abnormal cerebral cortex morphology J:185948
abnormal dendrite morphology J:185948
abnormal neocortex morphology J:185948
abnormal neuron morphology J:185948
abnormal parietal lobe morphology J:185948
abnormal somatosensory cortex morphology J:185948
abnormal visual cortex morphology J:185948
decreased brain size J:185948
thin cerebral cortex J:185948
Arhgap33tm1b(KOMP)Wtsi/Arhgap33+
C57BL/6N-Arhgap33tm1b(KOMP)Wtsi/Bay
decreased heart weight J:211773
unresponsive to tactile stimuli J:211773
Arhgap33tm1b(KOMP)Wtsi/Arhgap33tm1b(KOMP)Wtsi
C57BL/6N-Arhgap33tm1b(KOMP)Wtsi/Bay
preweaning lethality, incomplete penetrance J:211773
unresponsive to tactile stimuli J:211773

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
04/16/2024
MGI 6.23
The Jackson Laboratory