Symbol Name ID |
Pdss2
prenyl (solanesyl) diphosphate synthase, subunit 2 MGI:1918615 |
Darker colors indicate more annotations |
Human Phenotypes | Feeding difficulties |
Disease(s) Associated with PDSS2 | |
primary coenzyme Q10 deficiency 3 |
Mouse Phenotypes | polydipsia |
absent gastric milk in neonates |
dysphagia |
decreased anxiety-related response |
decreased thigmotaxis |
hunched posture |
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Availability | Mouse Genotype | ||||||
Pdss2kd/Pdss2kd | |||||||
Pdss2tm1b(EUCOMM)Hmgu/Pdss2+ | |||||||
Pdss2tm1.1Jdhu/Pdss2tm1.2Jdhu Tg(Pax2-cre)1Akg/0 (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 04/09/2024 MGI 6.23 |
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