Gene

phyh

ID
ZDB-GENE-050417-361
Name
phytanoyl-CoA 2-hydroxylase
Symbol
phyh Nomenclature History
Previous Names
  • zgc:110203
Type
protein_coding_gene
Location
Chr: 4 Mapping Details/Browsers
Description
Predicted to have phytanoyl-CoA dioxygenase activity. Predicted to be involved in fatty acid alpha-oxidation. Human ortholog(s) of this gene implicated in Refsum disease; Zellweger syndrome; orofacial cleft; and peroxisomal disease. Is expressed in intestinal bulb and liver. Orthologous to human PHYH (phytanoyl-CoA 2-hydroxylase).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
8 figures from 2 publications
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
Wild Type Expression Summary
Phenotype
All Phenotype Data
No data available
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With phyh Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
Refsum disease Alliance Refsum disease 266500
Associated With phyh Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Family IPR008775 Phytanoyl-CoA dioxygenase-like
Family IPR047128 Phytanoyl-CoA dioxygenase
Domain Details Per Protein
Protein Length Phytanoyl-CoA dioxygenase Phytanoyl-CoA dioxygenase-like
UniProtKB:Q5RHY0 335
Transcripts
Genome Browsers
Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
No data available
Constructs
Marker Relationships
Sequences
Orthology
Comparative Orthology
Alliance
Gene Tree
Ensembl
Citations