Gene Gene information from NCBI Gene database.
Entrez ID 92960
Gene name Peroxisomal biogenesis factor 11 gamma
Gene symbol PEX11G
Synonyms (NCBI Gene)
PEX11gamma
Chromosome 19
Chromosome location 19p13.2
Summary The protein encoded by this gene is a member of the PEX11 family. This family is reported to regulate the number and size of peroxisomes in evolutionarily distant organisms. The protein encoded by this gene may induce clustering of peroxisomes. Alternativ
miRNA miRNA information provided by mirtarbase database.
7
miRTarBase ID miRNA Experiments Reference
MIRT2591598 hsa-miR-1470 CLIP-seq
MIRT2591599 hsa-miR-1910 CLIP-seq
MIRT2591600 hsa-miR-2114 CLIP-seq
MIRT2591601 hsa-miR-3649 CLIP-seq
MIRT2591602 hsa-miR-455-3p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
12
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 20826455, 32296183
GO:0005777 Component Peroxisome IDA 20826455
GO:0005777 Component Peroxisome IEA
GO:0005778 Component Peroxisomal membrane IBA
GO:0005778 Component Peroxisomal membrane IDA 12559946
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
607583 20208 ENSG00000104883
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q96HA9
Protein name Peroxisomal membrane protein 11C (Peroxin-11C) (Peroxisomal biogenesis factor 11C) (Protein PEX11 homolog gamma) (PEX11-gamma)
Protein function Promotes membrane protrusion and elongation on the peroxisomal surface.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF05648 PEX11 4 230 Peroxisomal biogenesis factor 11 (PEX11) Family
Sequence
Sequence length 241
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG 
  Peroxisome  
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
PEROXISOME BIOGENESIS DISORDERS Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations