Details for: COX11

Gene ID: 1353

Symbol: COX11

Ensembl ID: ENSG00000166260

Description: cytochrome c oxidase copper chaperone COX11

Associated with

Other Information

Genular Protein ID: 1170855491

Symbol: COX11_HUMAN

Name: Cytochrome c oxidase assembly protein COX11, mitochondrial

UniProtKB Accession Codes:

Database IDs:

Citations:

PubMed ID: 9878253

Title: Identification and characterization of human cDNAs specific to BCS1, PET112, SCO1, COX15, and COX11, five genes involved in the formation and function of the mitochondrial respiratory chain.

PubMed ID: 9878253

DOI: 10.1006/geno.1998.5580

PubMed ID: 16625196

Title: DNA sequence of human chromosome 17 and analysis of rearrangement in the human lineage.

PubMed ID: 16625196

DOI: 10.1038/nature04689

PubMed ID: 15489334

Title: The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).

PubMed ID: 15489334

DOI: 10.1101/gr.2596504

PubMed ID: 9110174

Title: Large-scale concatenation cDNA sequencing.

PubMed ID: 9110174

DOI: 10.1101/gr.7.4.353

PubMed ID: 15229189

Title: Human SCO1 and SCO2 have independent, cooperative functions in copper delivery to cytochrome c oxidase.

PubMed ID: 15229189

DOI: 10.1093/hmg/ddh197

PubMed ID: 15840172

Title: Physical interaction and functional coupling between ACDP4 and the intracellular ion chaperone COX11, an implication of the role of ACDP4 in essential metal ion transport and homeostasis.

PubMed ID: 15840172

DOI: 10.1186/1744-8069-1-15

PubMed ID: 25944712

Title: N-terminome analysis of the human mitochondrial proteome.

PubMed ID: 25944712

DOI: 10.1002/pmic.201400617

PubMed ID: 34400285

Title: RANBP2 mutation causing autosomal dominant acute necrotizing encephalopathy attenuates its interaction with COX11.

PubMed ID: 34400285

DOI: 10.1016/j.neulet.2021.136173

PubMed ID: 36030551

Title: Biallelic pathogenic variants in COX11 are associated with an infantile-onset mitochondrial encephalopathy.

PubMed ID: 36030551

DOI: 10.1002/humu.24453

Sequence Information:

  • Length: 276
  • Mass: 31430
  • Checksum: 1F2BD22E1E7DD52D
  • Sequence:
  • MGGLWRPGWR CVPFCGWRWI HPGSPTRAAE RVEPFLRPEW SGTGGAERGL RWLGTWKRCS 
    LRARHPALQP PRRPKSSNPF TRAQEEERRR QNKTTLTYVA AVAVGMLGAS YAAVPLYRLY 
    CQTTGLGGSA VAGHASDKIE NMVPVKDRII KISFNADVHA SLQWNFRPQQ TEIYVVPGET 
    ALAFYRAKNP TDKPVIGIST YNIVPFEAGQ YFNKIQCFCF EEQRLNPQEE VDMPVFFYID 
    PEFAEDPRMI KVDLITLSYT FFEAKEGHKL PVPGYN

Genular Protein ID: 2659855836

Symbol: B4DEY8_HUMAN

Name: N/A

UniProtKB Accession Codes:

Database IDs:

Sequence Information:

  • Length: 171
  • Mass: 19371
  • Checksum: 8FDF72C3F69B6050
  • Sequence:
  • MLGASYAAVP LYRLYCQTTG LGGSAVAGHA SDKIENMVPV KDRIIKISFN ADVHASLQWN 
    FRPQQTEIYV VPGETALAFY RAKNPTDKPV IGISTYNIVP FEAGQYFNKI QCFCFEEQRL 
    NPQEEVDMPV FFYIDPEFAE DPRMIKVDLI TLSYTFFEAK EGHKLPVPGY N

Genular Protein ID: 1045021594

Symbol: B4DI26_HUMAN

Name: N/A

UniProtKB Accession Codes:

Database IDs:

Citations:

PubMed ID: 16625196

Title: DNA sequence of human chromosome 17 and analysis of rearrangement in the human lineage.

PubMed ID: 16625196

DOI: 10.1038/nature04689

Sequence Information:

  • Length: 230
  • Mass: 25978
  • Checksum: B0EEBC7FE01BDA8E
  • Sequence:
  • MGGLWRPGWR CVPFCGWRWI HPGSPTRAAE RVEPFLRPEW SGTGGAERGL RWLGTWKRCS 
    LRARHPALQP PRRPKSSNPF TRAQEEERRR QNKTTLTYVA AVAVGMLGAS YAAVPLYRLY 
    CQTTGLGGSA VAGHASDKIE NMVPVKDRII KISFNADVHA SLQWNFRPQQ TEIYVVPGET 
    ALAFYRAKNP TDKPVIGIST YNIVPFEAGQ YFNKIQVHQS VNFTEYDKDT

Database document:

This is a preview of the gene's schema. Only a few entries are kept for 'singleCellExpressions,' 'mRNAExpressions,' and other large data arrays for visualization purposes. You can zoom in with the mouse wheel for a closer view, and the text will adjust automatically if necessary. For the full schema, download it here.