Gene

pparg

ID
ZDB-GENE-990415-213
Name
peroxisome proliferator-activated receptor gamma
Symbol
pparg Nomenclature History
Previous Names
  • PPAR[g]
  • ARF6 (1)
  • NR1C3 (1)
  • nr1c3 (1)
Type
protein_coding_gene
Location
Chr: 11 Mapping Details/Browsers
Description
Predicted to enable DNA-binding transcription repressor activity, RNA polymerase II-specific; RNA polymerase II cis-regulatory region sequence-specific DNA binding activity; and nuclear receptor activity. Acts upstream of or within regulation of lipid metabolic process and triglyceride homeostasis. Predicted to be located in cytoplasm. Predicted to be active in nucleus. Is expressed in several structures, including adipose tissue; digestive system; female organism; male organism; and pleuroperitoneal region. Human ortholog(s) of this gene implicated in several diseases, including cardiovascular system disease (multiple); end stage renal disease; lipodystrophy (multiple); obesity; and type 2 diabetes mellitus. Orthologous to human PPARG (peroxisome proliferator activated receptor gamma).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
81 figures from 63 publications
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
Wild Type Expression Summary
Phenotype
All Phenotype Data
14 figures from 5 publications
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Allele Type Localization Consequence Mutagen Supplier
ecn6Allele with one delinsExon 2UnknownCRISPR
sa1220Allele with one point mutationUnknownPremature StopENU
sa1737Allele with one point mutationUnknownPremature StopENU
sa27703Allele with one point mutationUnknownPremature StopENU
sa34999Allele with one point mutationUnknownPremature StopENU
sa35000Allele with one point mutationUnknownSplice SiteENU
wi701Allele with one delinsUnknownUnknownTALEN
zf3729Allele with one deletionExon 2UnknownCRISPR
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Sequence Targeting Reagents
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Human Disease
Associated With pparg Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
familial partial lipodystrophy type 3 Alliance Lipodystrophy, familial partial, type 3 604367
obesity Alliance Obesity, severe 601665
type 2 diabetes mellitus Alliance Insulin resistance, severe, digenic 125853
type 2 diabetes mellitus Alliance {Diabetes, type 2} 125853
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Associated With pparg Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Domain IPR000536 Nuclear hormone receptor, ligand-binding domain
Domain IPR001628 Zinc finger, nuclear hormone receptor-type
Domain IPR022590 Peroxisome proliferator-activated receptor gamma, N-terminal
Family IPR001723 Nuclear hormone receptor
Family IPR003074 Peroxisome proliferator-activated receptor
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Domain Details Per Protein
Protein Additional Resources Length Nuclear hormone receptor Nuclear hormone receptor family NR1 subfamily Nuclear hormone receptor, ligand-binding domain Nuclear hormone receptor-like domain superfamily Peroxisome proliferator-activated receptor Peroxisome proliferator-activated receptor gamma Peroxisome proliferator-activated receptor gamma, N-terminal Zinc finger, NHR/GATA-type Zinc finger, nuclear hormone receptor-type
UniProtKB:A6XMH6 InterPro 527
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Transcripts
Genome Browsers
Genome Build: GRCz11Chromosome: 11
Type Name Annotation Method Has Havana Data Length (nt) Analysis
mRNA pparg-201 (1) Ensembl 1,359 nt
mRNA pparg-202 (1) Ensembl 535 nt
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Interactions and Pathways
Antibodies
No data available
Plasmids
Constructs
No data available
Marker Relationships
Relationship Marker Type Marker Accession Numbers Citations
EncodesESTdq017619Bertrand et al., 2007
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Sequences
Orthology
Comparative Orthology
Alliance
Gene Tree
Ensembl
Species Symbol Chromosome Accession # Evidence
HumanPPARG3
Phylogenetic tree (3)
Amino acid sequence comparison (5)
Conserved genome location (synteny) (2)
MousePparg6
Phylogenetic tree (2)
Conserved genome location (synteny) (1)
Amino acid sequence comparison (3)
Citations
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