Symbol Name ID |
Phyh
phytanoyl-CoA hydroxylase MGI:891978 |
Darker colors indicate more annotations |
Human Phenotypes | Microcephaly |
Anosmia |
Polymicrogyria |
Ataxia |
Abnormal pyramidal sign |
Hemiplegia/hemiparesis |
EEG abnormality |
Cognitive impairment |
Intellectual disability, severe |
Reduced tendon reflexes |
Developmental regression |
Profound global developmental delay |
Peripheral neuropathy |
Seizure |
Disease(s) Associated with PHYH | ||||||||||||||
Refsum disease | ||||||||||||||
Zellweger syndrome |
Mouse Phenotypes | decreased Purkinje cell number |
abnormal nervous system physiology |
abnormal astrocyte physiology |
abnormal action potential |
decreased nerve conduction velocity |
decreased prepulse inhibition |
|
Availability | Mouse Genotype | ||||||
Phyhtm1b(EUCOMM)Wtsi/Phyhtm1b(EUCOMM)Wtsi | |||||||
Phyhtm1Safe/Phyhtm1Safe |
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 07/02/2024 MGI 6.13 |
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