Phyh - phytanoyl-CoA 2-hydroxylase Gene

Rattus norvegicus

Gene ID: 114209 | Gene type: protein coding

About Phyh

Summary

Enables phytanoyl-CoA dioxygenase activity. Involved in 2-oxobutyrate catabolic process and fatty acid alpha-oxidation. Located in mitochondrion and peroxisome. Biomarker of non-alcoholic fatty liver disease. Human ortholog(s) of this gene implicated in Refsum disease; Zellweger syndrome; orofacial cleft; and peroxisomal disease. Orthologous to human PHYH (phytanoyl-CoA 2-hydroxylase). [provided by Alliance of Genome Resources, Apr 2022]

Phyh Products(1)

mRNA	Protein	Name
NM_053674.2	NP_446126.1	phytanoyl-CoA dioxygenase, peroxisomal precursor

Protein Preferred Names

Protein Names

phytanoyl-CoA dioxygenase, peroxisomal

phytanic acid oxidase	phytanoyl-CoA alpha-hydroxylase
phytanoyl-CoA hydroxylase (Refsum disease)

Related Agents

Pre-clinical Phase

Bioactive Molecules (3)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS10457	PHYH Human Pre-designed siRNA Set A	Pre-designed Set	/	Unkown
HY-RS19365	Phyh Mouse Pre-designed siRNA Set A	Pre-designed Set	/	Unkown
HY-RS25857	Phyh Rat Pre-designed siRNA Set A	Pre-designed Set	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Homo sapiens	Phyh	NCBI	NCBI:5264

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