Details for: KCNQ5

Gene ID: 56479

Symbol: KCNQ5

Ensembl ID: ENSG00000185760

Description: potassium voltage-gated channel subfamily Q member 5

Associated with

Other Information

Genular Protein ID: 2164988754

Symbol: KCNQ5_HUMAN

Name: Potassium voltage-gated channel subfamily KQT member 5

UniProtKB Accession Codes:

Database IDs:

Citations:

PubMed ID: 10787416

Title: Molecular cloning and functional expression of KCNQ5, a potassium channel subunit that may contribute to neuronal M-current diversity.

PubMed ID: 10787416

DOI: 10.1074/jbc.m002378200

PubMed ID: 14574404

Title: The DNA sequence and analysis of human chromosome 6.

PubMed ID: 14574404

DOI: 10.1038/nature02055

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: 14702039

Title: Complete sequencing and characterization of 21,243 full-length human cDNAs.

PubMed ID: 14702039

DOI: 10.1038/ng1285

PubMed ID: 10816588

Title: KCNQ5, a novel potassium channel broadly expressed in brain, mediates M-type currents.

PubMed ID: 10816588

DOI: 10.1074/jbc.m003245200

PubMed ID: 11159685

Title: Characterization of KCNQ5/Q3 potassium channels expressed in mammalian cells.

PubMed ID: 11159685

DOI: 10.1038/sj.bjp.0703861

PubMed ID: 23186163

Title: Toward a comprehensive characterization of a human cancer cell phosphoproteome.

PubMed ID: 23186163

DOI: 10.1021/pr300630k

PubMed ID: 24855057

Title: Functional assembly of Kv7.1/Kv7.5 channels with emerging properties on vascular muscle physiology.

PubMed ID: 24855057

DOI: 10.1161/atvbaha.114.303801

PubMed ID: 29429937

Title: A calmodulin C-lobe Ca(2+)-dependent switch governs Kv7 channel function.

PubMed ID: 29429937

DOI: 10.1016/j.neuron.2018.01.035

PubMed ID: 16959974

Title: The consensus coding sequences of human breast and colorectal cancers.

PubMed ID: 16959974

DOI: 10.1126/science.1133427

PubMed ID: 28669405

Title: Loss-of-function and gain-of-function mutations in KCNQ5 cause intellectual disability or epileptic encephalopathy.

PubMed ID: 28669405

DOI: 10.1016/j.ajhg.2017.05.016

Sequence Information:

  • Length: 932
  • Mass: 102179
  • Checksum: CB41C243FD2B00FC
  • Sequence:
  • MPRHHAGGEE GGAAGLWVKS GAAAAAAGGG RLGSGMKDVE SGRGRVLLNS AAARGDGLLL 
    LGTRAATLGG GGGGLRESRR GKQGARMSLL GKPLSYTSSQ SCRRNVKYRR VQNYLYNVLE 
    RPRGWAFIYH AFVFLLVFGC LILSVFSTIP EHTKLASSCL LILEFVMIVV FGLEFIIRIW 
    SAGCCCRYRG WQGRLRFARK PFCVIDTIVL IASIAVVSAK TQGNIFATSA LRSLRFLQIL 
    RMVRMDRRGG TWKLLGSVVY AHSKELITAW YIGFLVLIFS SFLVYLVEKD ANKEFSTYAD 
    ALWWGTITLT TIGYGDKTPL TWLGRLLSAG FALLGISFFA LPAGILGSGF ALKVQEQHRQ 
    KHFEKRRNPA ANLIQCVWRS YAADEKSVSI ATWKPHLKAL HTCSPTKKEQ GEASSSQKLS 
    FKERVRMASP RGQSIKSRQA SVGDRRSPST DITAEGSPTK VQKSWSFNDR TRFRPSLRLK 
    SSQPKPVIDA DTALGTDDVY DEKGCQCDVS VEDLTPPLKT VIRAIRIMKF HVAKRKFKET 
    LRPYDVKDVI EQYSAGHLDM LCRIKSLQTR VDQILGKGQI TSDKKSREKI TAEHETTDDL 
    SMLGRVVKVE KQVQSIESKL DCLLDIYQQV LRKGSASALA LASFQIPPFE CEQTSDYQSP 
    VDSKDLSGSA QNSGCLSRST SANISRGLQF ILTPNEFSAQ TFYALSPTMH SQATQVPISQ 
    SDGSAVAATN TIANQINTAP KPAAPTTLQI PPPLPAIKHL PRPETLHPNP AGLQESISDV 
    TTCLVASKEN VQVAQSNLTK DRSMRKSFDM GGETLLSVCP MVPKDLGKSL SVQNLIRSTE 
    ELNIQLSGSE SSGSRGSQDF YPKWRESKLF ITDEEVGPEE TETDTFDAAP QPAREAAFAS 
    DSLRTGRSRS SQSICKAGES TDALSLPHVK LK

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.