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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Ccr10
C-C motif chemokine receptor 10
MGI:1096320
31 phenotypes from 3 alleles in 4 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Ccr10/Cntnap1tm1Bhat/Ccr10/Cntnap1tm1Bhat
involves: 129S7/SvEvBrd
abnormal action potential J:69621
abnormal axon morphology J:69621
abnormal cerebellar molecular layer J:162215
abnormal gait J:69621, J:107653
abnormal myelin sheath morphology J:69621, J:162215
abnormal nerve conduction J:342323
abnormal Purkinje cell axon morphology J:107653, J:162215
abnormal Purkinje cell morphology J:107653, J:162215
ataxia J:69621, J:107653
decreased body size J:69621
decreased body weight J:69621
decreased locomotor activity J:69621
decreased nerve conduction velocity J:69621, J:342323
dysmyelination J:342323
hypermyelination J:69621
impaired balance J:69621
impaired coordination J:107653
impaired fine motor coordination J:342323
kyphosis J:69621
lethality at weaning, incomplete penetrance J:69621
muscle spasm J:69621
paresis J:69621
premature death J:69621
tremors J:69621
weakness J:69621
Ccr10tm1.1Nax/Ccr10tm1.1Nax
B6.129S4(Cg)-Ccr10tm1.1Nax
decreased gamma-delta intraepithelial T cell number J:165323
Ccr10tm1Cge/Ccr10tm1Cge
C.129S4-Ccr10tm1Cge
abnormal leukocyte migration J:140728
abnormal milk composition J:140728
abnormal plasma cell morphology J:140728
decreased IgA level J:140728
Ccr10tm1Cge/Ccr10tm1Cge
involves: 129S4/SvJae
no abnormal phenotype detected J:69621

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
12/10/2024
MGI 6.24
The Jackson Laboratory