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Symbol Name ID |
Pdss2
prenyl (solanesyl) diphosphate synthase, subunit 2 MGI:1918615 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Proteinuria |
Nephrotic syndrome |
| Disease(s) Associated with PDSS2 | ||
| primary coenzyme Q10 deficiency 3 |
| Mouse Phenotypes | renal/urinary system phenotype |
kidney cyst |
colorless urine |
albuminuria |
tubulointerstitial nephritis |
abnormal kidney morphology |
abnormal glomerular capsule parietal layer morphology |
abnormal podocyte morphology |
podocyte foot process effacement |
abnormal renal glomerulus basement membrane morphology |
abnormal renal glomerulus morphology |
glomerulosclerosis |
renal interstitial fibrosis |
kidney atrophy |
renal tubule atrophy |
abnormal renal tubule morphology |
dilated renal tubule |
renal cast |
granular kidney |
pale kidney |
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| Availability | Mouse Genotype | ||||||||||||||||||||
| Pdss2kd/Pdss2kd | |||||||||||||||||||||
| Pdss2tm1Dalg/Pdss2tm1Dalg | * | ||||||||||||||||||||
| Pdss2tm1Dalg/Pdss2tm1Dalg Tg(NPHS2-cre)295Lbh/? (conditional) |
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| Pdss2tm1Dalg/Pdss2tm1Dalg Hprt1tm1(Pck1-cre)Vhh/? (conditional) |
* | ||||||||||||||||||||
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 04/23/2024 MGI 6.23 |
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