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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Cntnap4
contactin associated protein-like 4
MGI:2183572
14 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Cntnap4em1Smoc/Cntnap4em1Smoc
C57BL/6J-Cntnap4em1Smoc
abnormal substantia nigra pars compacta morphology J:287186
decreased locomotor activity J:287186
enhanced autophagy J:287186
impaired coordination J:287186
neuron degeneration J:287186
Cntnap4tm1Pele/Cntnap4+
involves: 129S1/Sv * 129X1/SvJ * ICR
abnormal postsynaptic density morphology J:211338
abnormal prepulse inhibition J:211338
abnormal synapse morphology J:211338
increased dopamine level J:211338
increased grooming behavior J:211338
increased startle reflex J:211338
Cntnap4tm1Pele/Cntnap4tm1Pele
involves: 129S1/Sv * 129X1/SvJ * ICR
abnormal inhibitory postsynaptic currents J:211338
abnormal miniature inhibitory postsynaptic currents J:211338
abnormal postsynaptic density morphology J:211338
abnormal prepulse inhibition J:211338
abnormal synapse morphology J:211338
increased dopamine level J:211338
increased grooming behavior J:211338
increased startle reflex J:211338
seizures J:211338

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
04/30/2024
MGI 6.23
The Jackson Laboratory