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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Pycr2
pyrroline-5-carboxylate reductase family, member 2
MGI:1277956
49 phenotypes from 3 alleles in 4 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Pycr2m1J/Pycr2m1J
involves: C3H/HeJ * C57BL/6J
abnormal axon morphology J:308336
abnormal gait J:308336
decreased basophil cell number J:308336
decreased body weight J:308336
decreased circulating cholesterol level J:308336
decreased circulating glutamic acid level J:308336
decreased circulating HDL cholesterol level J:308336
decreased circulating potassium level J:308336
decreased circulating triglyceride level J:308336
decreased grip strength J:308336
decreased leukocyte cell number J:308336
decreased lymphocyte cell number J:308336
decreased subcutaneous adipose tissue amount J:308336
decreased total body fat amount J:308336
normal homeostasis/metabolism phenotype J:308336
increased blood urea nitrogen level J:308336
increased myelin sheath thickness J:308336
kyphosis J:308336
limb grasping J:308336
normal nervous system phenotype J:308336
renal glomerulus lipidosis J:308336
normal skeleton phenotype J:308336
thin body J:308336
thin skin J:308336
Pycr2m1J/Pycr2m1J
Pycr2m1J/Pycr2m1J
involves: C3H/HeJ * C57BL/6J * C57BL/6NTac
decreased body size J:308336
preweaning lethality, incomplete penetrance J:308336
Pycr2tm1.1Brre/Pycr2tm1.1Brre
involves: C57BL/6
abnormal amino acid level J:296329
abnormal neuron morphology J:296329
abnormal oligodendrocyte apoptosis J:296329
abnormal oligodendrocyte morphology J:296329
axonal dystrophy J:296329
axonal spheroids J:296329
decreased body mass index J:296329
decreased corpus callosum size J:296329
hippocampal neuron degeneration J:296329
impaired balance J:296329
impaired coordination J:296329
impaired neuron differentiation J:296329
increased neuron apoptosis J:296329
kyphosis J:296329
limb grasping J:296329
neuron degeneration J:296329
premature death J:296329
weight loss J:296329
Pycr2tm1a(EUCOMM)Wtsi/Pycr2tm1a(EUCOMM)Wtsi
C57BL/6N-Pycr2tm1a(EUCOMM)Wtsi/Wtsi
absent pinna reflex J:211773
decreased bone mineral density J:211773
decreased Ly6C low monocyte number J:211773
decreased monocyte cell number J:211773
increased fasting circulating glucose level J:211773
increased mean corpuscular hemoglobin J:211773
limb grasping J:211773
trunk curl 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