AFG3L2, AFG3 like matrix AAA peptidase subunit 2

AFG3L2, AFG3 like matrix AAA peptidase subunit 2

• This gene encodes a protein localized in mitochondria and closely related to paraplegin. The paraplegin gene is responsible for an autosomal recessive form of hereditary spastic paraplegia. This gene is a candidate gene for other hereditary spastic paraplegias or neurodegenerative disorders. [provided by RefSeq, Jul 2008]

• Gene Synonyms (SCA28, SPAX5, AFG3-like protein 2, AFG3 ATPase family gene 3-like 2, AFG3 ATPase family member 3-like 2, AFG3 like AAA ATPase 2, ATPase family gene 3, yeast, paraplegin-like protein,)
• NCBI Gene ID: 10939
• Species: Homo sapiens (Human)
• UNIPROT ID#>>Q9Y4W6
  UNIPROT ID#>>Q8TA92
• View the NCBI Database for this Gene »

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

AFG3 like matrix AAA peptidase subunit 2 interacts with:

• AFG3 like matrix AAA peptidase subunit 2
  anoctamin 7
  armadillo repeat containing 8
  aurora kinase A interacting protein 1
  bone morphogenetic protein receptor, type 1A
  bromodomain containing 7
  CDGSH iron sulfur domain 3
  centromere protein E
  chromosome 15 open reading frame 48
  coenzyme Q2, polyprenyltransferase
  coenzyme Q9
  coiled-coil domain containing 58
  coiled-coil domain containing 8
  coiled-coil-helix-coiled-coil-helix domain containing 2
  cytochrome c oxidase assembly factor 3
  cytochrome c oxidase assembly factor COX14
  dual specificity phosphatase 26
  egl-9 family hypoxia inducible factor 3
  elongation factor for RNA polymerase II 2
  F-box protein 6
  glucosylceramidase beta 2
  glutamate rich WD repeat containing 1
  heat shock protein 14
  homeodomain interacting protein kinase 4
  hydroxysteroid 17-beta dehydrogenase 12
  inturned planar cell polarity protein
  jun B proto-oncogene
  matrix AAA peptidase interacting protein 1
  membrane spanning 4-domains A4A
  mitochondrial contact site and cristae organizing system subunit 10
  mitochondrial rRNA methyltransferase 1
  mitogen-activated protein kinase 8 interacting protein 2
  NADH:ubiquinone oxidoreductase subunit A11
  NADH:ubiquinone oxidoreductase subunit A13
  NEDD1 gamma-tubulin ring complex targeting factor
  OCIA domain containing 1
  pleckstrin homology domain containing A4
  potassium channel tetramerisation domain containing 5
  prohibitin 2
  protein tyrosine phosphatase mitochondrial 1
  pyruvate dehyrogenase phosphatase catalytic subunit 2
  receptor interacting serine/threonine kinase 4
  ring finger protein 31
  RNA binding motif protein 45
  serine/threonine/tyrosine interacting like 1
  sideroflexin 1
  slingshot protein phosphatase 1
  survival motor neuron 1
  SUZ12 polycomb repressive complex 2 subunit
  thyroid hormone receptor interactor 11
  translocase of inner mitochondrial membrane domain containing 1
  translocase of outer mitochondrial membrane 22
  transmembrane and coiled-coil domains 1
  transmembrane protein 41B
  transportin 1
  trimethylguanosine synthase 1
  tRNA methyltransferase 61B
  tubulin alpha 1c
  tubulin, gamma 1
  ubiquilin 2
  ubiquinol-cytochrome c reductase complex III subunit VII
  ubiquitin specific peptidase 50
  vir like m6A methyltransferase associated
  WW domain containing oxidoreductase
  YTH domain containing 1

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.