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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Prnd
prion like protein doppel
MGI:1346999
14 phenotypes from 4 alleles in 4 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Prndtm1Aag/Prndtm1Aag
involves: 129P2/OlaHsd
abnormal acrosome morphology J:91621
abnormal sperm head morphology J:91621
abnormal spermiogenesis J:91621
asthenozoospermia J:91621
hairpin sperm flagellum J:91621
impaired sperm penetration of zona pellucida J:91621
male infertility J:91621
oligozoospermia J:91621
teratozoospermia J:91621
Prndtm1Dwm/Prndtm1Dwm
129P2/OlaHsd-Prndtm1Dwm
impaired acrosome reaction J:91094
impaired fertilization J:91094
male infertility J:91094
Prnp/Prndtm1Aag/Prnp/Prndtm1Aag
Not Specified
normal behavior/neurological phenotype J:89232
normal immune system phenotype J:89232
male infertility J:89232
normal nervous system phenotype J:89232
teratozoospermia J:89232
Prnp/Prndtm1Dwm/Prnp/Prndtm1Dwm
129P2/OlaHsd-Prnp/Prndtm1Dwm
impaired acrosome reaction J:91094
impaired fertilization J:91094
male infertility J:91094

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
05/07/2024
MGI 6.23
The Jackson Laboratory