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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Rgn
regucalcin
MGI:108024
34 phenotypes from 1 allele in 2 genetic backgrounds
Export: Excel File
Allelic Composition
Genetic Background
Annotated Term Reference
Rgntm1Aish/Y
involves: 129P2/OlaHsd
abnormal amino acid level J:108295
abnormal brain morphology J:107922
abnormal circulating amino acid level J:108295
abnormal enzyme/coenzyme activity J:108295
abnormal gait J:108295
abnormal hair cycle J:150664
abnormal hepatocyte mitochondrial morphology J:88791
abnormal hepatocyte morphology J:88791
abnormal keratinocyte morphology J:150664
abnormal liver vasculature morphology J:88791
abnormal phospholipid level J:88791
abnormal pulmonary acinus morphology J:101810, J:135721
abnormal vitamin C level J:108295, J:150664
decreased body weight J:88791
decreased bone mineral density J:108295
decreased hydroxyproline level J:150664
decreased percent body fat/body weight J:108295
emphysema J:135721
femur fracture J:108295
hepatic steatosis J:88791
increased cellular sensitivity to oxidative stress J:135721
increased liver cholesterol level J:88791
increased liver triglyceride level J:88791
increased susceptibility to induced morbidity/mortality J:108295
oxidative stress J:107922, J:135721
premature death J:88791
rachitic rosary J:108295
thin dermal layer J:150664
weight loss J:108295, J:135721
Rgntm1Aish/Y
involves: 129P2/OlaHsd * C57BL/6
abnormal vitamin C level J:155625, J:191530
alopecia J:155625
anterior subcapsular cataract J:191530
cochlear ganglion degeneration J:155625
increased or absent threshold for auditory brainstem response J:155625
Rgntm1Aish/Rgntm1Aish
involves: 129P2/OlaHsd * C57BL/6
abnormal vitamin C level J:191530
anterior subcapsular cataract J:191530
increased hepatocyte apoptosis J:79342

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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
11/12/2024
MGI 6.24
The Jackson Laboratory