PEX2

protein-coding gene in the species Homo sapiens

DBpedia resource is: http://dbpedia.org/resource/Peroxisomal_biogenesis_factor_2

Abstract is: Peroxisomal biogenesis factor 2 is a protein that in humans is encoded by the PEX2 gene. This gene encodes an integral peroxisomal membrane protein required for peroxisome biogenesis. The protein is thought to be involved in peroxisomal matrix protein import. Mutations in this gene result in one form of Zellweger syndrome and infantile Refsum disease. Alternative splicing results in multiple transcript variants encoding the same protein.

PEX2 is …
instance of (P31):
geneQ7187

sublass of (P279):
protein-coding geneQ20747295

External links are
P594Ensembl gene IDENSG00000164751
P704Ensembl transcript IDENST00000357039
ENST00000518986
ENST00000519956
ENST00000520103
ENST00000520203
ENST00000522527
P351Entrez Gene ID5828
P2888exact matchhttp://identifiers.org/ncbigene/5828
P646Freebase ID/m/03gy8wf
P353HGNC gene symbolPEX2
P354HGNC ID9717
P593HomoloGene ID269
P492OMIM ID170993
170993
P639RefSeq RNA IDNM_000318
NM_001079867
NM_001172086
NM_001172087
P2892UMLS CUIC1419149

P1057chromosomehuman chromosome 8Q572848
P4196cytogenetic location8q21.13
P688encodesperoxisomal biogenesis factor 2Q21122491
P5572expressed ingallbladderQ64386
monocyteQ107244
rectumQ158716
body of pancreasQ4936946
islet of LangerhansQ728309
seminal vesiculaQ217259
ventricular zoneQ28455175
right adrenal cortexQ66566695
olfactory zone of nasal mucosaQ66574757
epithelium of colonQ66714209
P703found in taxonHomo sapiensQ15978631
P2293genetic associationZellweger syndromeQ189167
Zellweger spectrum disorderQ51250082
peroxisomal biogenesis disorderQ61913385
P645genomic end77001044
77913280
P644genomic start76980258
77892494
P684orthologPex2Q18253378
Pex2Q24365476
Pex2Q29724576
pex2Q29763676
P2548strand orientationreverse strandQ22809711

Wikimedia Commons Images

P692: Gene Atlas image


FileName: PBB GE PXMP3 210296 s at fs.png

Description: Gene expression pattern of the PXMP3 gene.

Artist: AndrewGNF at en.wikipedia

Work is copyrighted.
License: CC BY-SA 3.0
Attribution is required.

Reverse relations

regulates (molecular biology) (P128)
Q27594174hsa-miR-1285-3p
Q27593250hsa-miR-135a-5p
Q27592894hsa-miR-135b-5p
Q27593806hsa-miR-142-5p
Q27594719hsa-miR-143-5p
Q27595209hsa-miR-188-3p
Q27593208hsa-miR-196a-3p
Q27592868hsa-miR-214-5p
Q27593961hsa-miR-24-3p
Q27593849hsa-miR-3065-5p
Q27593914hsa-miR-3187-5p
Q27594749hsa-miR-340-5p
Q27594902hsa-miR-3609
Q27593254hsa-miR-3652
Q27594889hsa-miR-4284
Q27593888hsa-miR-4318
Q27592925hsa-miR-4427
Q27594149hsa-miR-4430
Q27593384hsa-miR-4505
Q27593009hsa-miR-4680-3p
Q27594434hsa-miR-4762-3p
Q27594277hsa-miR-4786-5p
Q27593402hsa-miR-493-3p
Q27592853hsa-miR-5187-3p
Q27593685hsa-miR-5189-5p
Q27594087hsa-miR-520g-3p
Q27594098hsa-miR-520h
Q27594331hsa-miR-548ag
Q27594609hsa-miR-548ah-5p
Q27594824hsa-miR-548ai
Q27594153hsa-miR-548ba
Q27593942hsa-miR-5589-5p
Q27594205hsa-miR-5590-3p
Q27593309hsa-miR-5693
Q27594573hsa-miR-570-5p
Q27594491hsa-miR-5787
Q27592942hsa-miR-6072
Q27593116hsa-miR-612
Q27594726hsa-miR-6499-3p
Q27593100hsa-miR-6514-3p
Q27593492hsa-miR-656-3p
Q27595048hsa-miR-661
Q27592913hsa-miR-6741-5p
Q27593696hsa-miR-6776-5p
Q27594271hsa-miR-6811-3p
Q27594981hsa-miR-6842-3p
Q27595052hsa-miR-6847-3p
Q27595062hsa-miR-6849-3p
Q27593121hsa-miR-6860
Q27594773hsa-miR-6891-3p
Q27594008hsa-miR-769-5p
Q27594514hsa-miR-8060
Q27594031hsa-miR-8074
Q27593460hsa-miR-889-5p
Q27595059hsa-miR-939-3p

genetic association (P2293)
Q16965307Neonatal adrenoleukodystrophy
Q51250082Zellweger spectrum disorder
Q189167Zellweger syndrome
Q61913385peroxisomal biogenesis disorder

ortholog (P684)
Q18253378Pex2
Q24365476Pex2
Q29724576Pex2
Q29763676pex2

Q21122491peroxisomal biogenesis factor 2encoded byP702

The articles in Wikimedia projects and languages

      Peroxisomal biogenesis factor 2wikipedia
Tatar language (tt / Q25285)PEX2wikipedia
      PEX2wikipedia

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