Browse our PEX10 Proteins (PEX10)

Full name:
Peroxisomal Biogenesis Factor 10 Proteins (PEX10)
On www.antibodies-online.com are 7 Peroxisomal Biogenesis Factor 10 (PEX10) Proteins from 3 different suppliers available. Additionally we are shipping PEX10 Antibodies (31) and many more products for this protein. A total of 45 PEX10 products are currently listed.
Synonyms:
ATPEX10, AV128229, Gm142, NALD, PBD6A, PBD6B, peroxin 10, RNF69, T9J22.2
list all proteins Gene Name GeneID UniProt
PEX10 5192 O60683
PEX10 668173 B1AUE5
Rat PEX10 PEX10 680424  

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PEX10 Proteins (PEX10) by Origin

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More Proteins for PEX10 Interaction Partners

Arabidopsis thaliana Peroxisomal Biogenesis Factor 10 (PEX10) interaction partners

  1. PEX2 (show PEX2 Proteins) and PEX10 cooperate to support import of matrix proteins into plant peroxisomes and peroxin5 retrotranslocation in Arabidopsis.

  2. Data show that formation of glyoxysomal reticulum seemed to be impaired in PEX10-DeltaZn but not in PEX2 (show PEX2 Proteins)-DeltaZn-T7 or PEX12 (show PEX12 Proteins)-DeltaZn-T7 plants.

  3. PEX2 (show PEX2 Proteins) and PEX10 are inserted into peroxisome membranes directly from the cytosol.

  4. AtPEX19-1 was shown to bind to the Arabidopsis peroxisomal membrane protein PEX10.

  5. inactivation of the RING finger (show PCGF1 Proteins) domain in PEX10 has eliminated protein interaction required for attachment of peroxisomes to chloroplasts and movement of metabolites between peroxisomes and chloroplasts

Human Peroxisomal Biogenesis Factor 10 (PEX10) interaction partners

  1. This study demonstrated that two mutations in PEX10 were found in the three peroxisomal biogenesis disorders patients: c.827G>T (novel) causing the missense change p.Cys276Phe and c.932G>A causing the missense change p.Arg311Gln.

  2. abnormal expression of PEX10 gene resulting from copy number variations of 1p36 region may be associated with the epilepsy phenotype

  3. child and an adult of normal intelligence with progressive ataxia (show USP14 Proteins), axonal motor neuropathy, decreased vibration sense and cerebellar atrophy; 2 mutations in PEX10 found in child, c.992G>A and c.764_765insA, and in the adult, c.2T>C and c.790C>T

  4. Genetic heterogeneity in Japanese patients with peroxisome biogenesis disorders and evidence for a founder haplotype for the most common mutation in PEX10 gene.

  5. the relative fraction of disease-causing alleles that occur in the coding and splice junction sequences of PEX10 gene.

PEX10 Protein Profile

Protein Summary

This gene encodes a protein involved in import of peroxisomal matrix proteins. This protein localizes to the peroxisomal membrane. Mutations in this gene result in phenotypes within the Zellweger spectrum of peroxisomal biogenesis disorders, ranging from neonatal adrenoleukodystrophy to Zellweger syndrome. Alternative splicing results in two transcript variants encoding different isoforms.

Alternative names and synonyms associated with PEX10

  • peroxin 10 (PEX10)
  • peroxisomal biogenesis factor 10 (PEX10)
  • peroxisomal biogenesis factor 10 (Pex10)
  • ATPEX10 protein
  • AV128229 protein
  • Gm142 protein
  • NALD protein
  • PBD6A protein
  • PBD6B protein
  • peroxin 10 protein
  • RNF69 protein
  • T9J22.2 protein

Protein level used designations for PEX10

RING finger protein 69 , peroxin 10 , peroxin-10 , peroxisome assembly protein 10 , peroxisome biogenesis factor 10 , peroxisomal biogenesis factor 10

GENE ID SPECIES
817175 Arabidopsis thaliana
5192 Homo sapiens
419396 Gallus gallus
489612 Canis lupus familiaris
614539 Bos taurus
668173 Mus musculus
680424 Rattus norvegicus
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