About   Help   FAQ
Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Galc
galactosylceramidase
MGI:95636
76 phenotypes from 10 alleles in 14 genetic backgrounds
Export: Excel File
Allelic Composition
Genetic Background
Annotated Term Reference
GalcM1Btlr/Galc+
C57BL/6J-GalcM1Btlr
decreased body weight J:255205
GalcM1Btlr/GalcM1Btlr
C57BL/6J-GalcM1Btlr
decreased body weight J:255205
Galcm2Btlr/Galcm2Btlr
C57BL/6J-Galcm2Btlr
ataxia J:267485
decreased body size J:267485
decreased heart rate J:267485
increased mean systemic arterial blood pressure J:267485
increased systemic arterial diastolic blood pressure J:267485
Galcm3Btlr/Galcm3Btlr
C57BL/6J-Galcm3Btlr
ataxia J:274842
hindlimb paralysis J:274842
Galcm4Btlr/Galcm4Btlr
C57BL/6J-Galcm4Btlr
abnormal vertebral column morphology J:307652
decreased body size J:307652
kyphosis J:307652
Galctm1Wngr/Galctm1Wngr
involves: 129S2/SvPas
abnormal enzyme/coenzyme activity J:78691
abnormal immune system physiology J:78691
cachexia J:78691
demyelination J:78691
hindlimb paralysis J:78691
premature death J:78691
tremors J:78691
Galctwi-2J/Galctwi-2J
B10.A-H2i5/(R5)SgSn
abnormal gait J:78474
tremors J:78474
Galctwi-4J/Galctwi-4J
involves: C57BL/6J
ataxia J:137512
tremors J:137512
Galctwi-5J/Galctwi-5J
BXD32/TyJ-Galctwi-5J/J
abnormal axon morphology J:199132
abnormal corpus callosum morphology J:199132
abnormal leukocyte morphology J:199132
abnormal spinal cord morphology J:199132
astrocytosis J:199132
cachexia J:139715
decreased body size J:139715, J:199132
demyelination J:139715, J:199132
gliosis J:199132
postnatal lethality, incomplete penetrance J:139715
premature death J:199132
slow postnatal weight gain J:199132
tremors J:139715, J:199132
normal vision/eye phenotype J:139715
weakness J:199132
Galctwi/Galctwi-3J
involves: C57BL/6J * CE/J
decreased body size J:30778
tremors J:30778
Galctwi/Galctwi
B6.CE-Galctwi/J
abnormal astrocyte morphology J:108359, J:126892
abnormal bone remodeling J:165361
abnormal brain morphology J:126892
abnormal enzyme/coenzyme activity J:108359
abnormal forebrain morphology J:170081
abnormal gait J:126892
abnormal hindbrain morphology J:126892
abnormal lipid level J:165361
abnormal long bone metaphysis morphology J:165361
abnormal microglial cell morphology J:108359
abnormal oligodendrocyte morphology J:170081
abnormal osteoclast physiology J:165361
abnormal sciatic nerve morphology J:126892
abnormal skeleton development J:165361
abnormal sphingomyelin level J:165361
astrocytosis J:170081
ataxia J:108359
decreased body weight J:165361
decreased bone mineral density J:165361
decreased bone trabecula number J:165361
decreased circulating insulin-like growth factor I level J:165361
decreased compact bone thickness J:165361
decreased femur size J:165361
decreased femur weight J:165361
decreased oligodendrocyte number J:170081
demyelination J:108359, J:126892, J:170081
impaired righting response J:108359
increased oligodendrocyte progenitor number J:170081
muscle twitch J:170081
paraparesis J:126892
paresis J:170081
premature death J:108359, J:126892, J:170081
tremors J:108359, J:126892
weight loss J:170081
Galctwi/Galctwi
involves: 129P2/OlaHsd * C57BL/6J * CE/J
premature death J:63197
Galctwi/Galctwi
Il6+/?
involves: 129S2/SvPas * C57BL/6J * CE/J
abnormal blood-brain barrier function J:56656
abnormal cerebellum white matter morphology J:56656
abnormal tumor necrosis factor level J:56656
demyelination J:56656
gliosis J:56656
premature death J:56656
tremors J:56656
Galctwi/Galctwi
involves: C57BL/6J * CAST/EiJ * CE/J
abnormal astrocyte morphology J:126892
abnormal brain morphology J:126892
abnormal gait J:126892
abnormal hindbrain morphology J:126892
abnormal medulla oblongata morphology J:126892
abnormal pons morphology J:126892
abnormal sciatic nerve morphology J:126892
axonal spheroids J:126892
demyelination J:126892
paraparesis J:126892
premature death J:126892
tremors J:126892
Galctwi/Galctwi
involves: C57BL/6J * CE/J
abnormal macrophage morphology J:6390
abnormal myelin sheath morphology J:6390
cachexia J:6390
premature death J:6390
progressive muscle weakness J:6390
tremors J:6390
Galctwi/Galctwi
involves: CE/J
abnormal brain white matter morphology J:13867
abnormal glial cell apoptosis J:57215
abnormal kidney development J:7313
abnormal kidney epithelium morphology J:7313
abnormal kidney morphology J:7313
abnormal kidney physiology J:7311
abnormal lipid level J:78223
abnormal nervous system physiology J:7115
abnormal oligodendrocyte morphology J:57215
abnormal protein level J:7311
abnormal spinal cord white matter morphology J:13867
axon degeneration J:13867
CNS inflammation J:78223
decreased body size J:13867
decreased oligodendrocyte number J:57215
demyelination J:13867, J:78223
edema J:7115
hindlimb paralysis J:13867
impaired limb coordination J:13867
peripheral nervous system degeneration J:13867
normal renal/urinary system phenotype J:7313
tremors J:13867

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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
11/12/2024
MGI 6.24
The Jackson Laboratory