PEX10 Proteine (PEX10)

Bezeichnung:: Peroxisomal Biogenesis Factor 10 Proteine (PEX10)

Auf www.antikoerper-online.de finden Sie aktuell 7 Peroxisomal Biogenesis Factor 10 (PEX10) Proteine von 3 unterschiedlichen Herstellern. Zusätzlich bieten wir Ihnen PEX10 Antikörper (37) und viele weitere Produktgruppen zu diesem Protein an. Insgesamt sind aktuell 51 PEX10 Produkte verfügbar.

Synonyme:: ATPEX10, AV128229, Gm142, NALD, PBD6A, PBD6B, peroxin 10, RNF69, T9J22.2

alle Proteine anzeigen	Gen	GeneID	UniProt
	PEX10	5192	O60683
	PEX10	668173	B1AUE5
Ratte PEX10	PEX10	680424
Weitere Synonyme anzeigen

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Verknüpfte Pathways mit PEX10 Proteine

Monocarboxylic Acid Catabolic Process

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Weitere Proteine zu PEX10 Interaktionspartnern

Arabidopsis thaliana Peroxisomal Biogenesis Factor 10 (PEX10) Interaktionspartner

PEX2 (zeige PEX2 Proteine) and PEX10 cooperate to support import of matrix proteins into plant peroxisomes and peroxin5 retrotranslocation in Arabidopsis.
Data show that formation of glyoxysomal reticulum seemed to be impaired in PEX10-DeltaZn but not in PEX2 (zeige PEX2 Proteine)-DeltaZn-T7 or PEX12 (zeige PEX12 Proteine)-DeltaZn-T7 plants.
PEX2 (zeige PEX2 Proteine) and PEX10 are inserted into peroxisome membranes directly from the cytosol.
AtPEX19-1 was shown to bind to the Arabidopsis peroxisomal membrane protein PEX10.
inactivation of the RING finger (zeige PCGF1 Proteine) 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) Interaktionspartner

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.
abnormal expression of PEX10 gene resulting from copy number variations of 1p36 region may be associated with the epilepsy phenotype
child and an adult of normal intelligence with progressive ataxia, 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
Genetic heterogeneity in Japanese patients with peroxisome biogenesis disorders and evidence for a founder haplotype for the most common mutation in PEX10 gene.
the relative fraction of disease-causing alleles that occur in the coding and splice junction sequences of PEX10 gene.

PEX10 Protein Überblick

Protein Überblick

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

Bezeichner auf Proteinebene für PEX10

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

GENE ID	SPEZIES
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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