Gene

pex19

ID
ZDB-GENE-050417-424
Name
peroxisomal biogenesis factor 19
Symbol
pex19 Nomenclature History
Previous Names
  • pxf (1)
  • wu:fb40d12
  • wu:fc41h09
  • zgc:110675
Type
protein_coding_gene
Location
Chr: 2 Mapping Details/Browsers
Description
Predicted to localize to integral component of membrane and peroxisome. Human ortholog(s) of this gene implicated in peroxisome biogenesis disorder 12A. Orthologous to human PEX19 (peroxisomal biogenesis factor 19).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
1 figure from Thisse et al., 2004
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 pex19 Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
peroxisome biogenesis disorder 12A Alliance Peroxisome biogenesis disorder 12A (Zellweger) 614886
Associated With pex19 Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Family IPR006708 Pex19 protein
Homologous_superfamily IPR038322 Pex19, C-terminal domain superfamily
Domain Details Per Protein
Protein Length Pex19, C-terminal domain superfamily Pex19 protein
UniProtKB:Q561W9 288
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