Details for: HCN4

Gene ID: 10021

Symbol: HCN4

Ensembl ID: ENSG00000138622

Description: hyperpolarization activated cyclic nucleotide gated potassium channel 4

Associated with

Other Information

Genular Protein ID: 2215846694

Symbol: HCN4_HUMAN

Name: Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 4

UniProtKB Accession Codes:

Database IDs:

Citations:

PubMed ID: 10228147

Title: Two pacemaker channels from human heart with profoundly different activation kinetics.

PubMed ID: 10228147

DOI: 10.1093/emboj/18.9.2323

PubMed ID: 10430953

Title: Molecular characterization of a slowly gating human hyperpolarization-activated channel predominantly expressed in thalamus, heart, and testis.

PubMed ID: 10430953

DOI: 10.1073/pnas.96.16.9391

PubMed ID: 19165230

Title: Role of HCN4 channel in preventing ventricular arrhythmia.

PubMed ID: 19165230

DOI: 10.1038/jhg.2008.16

PubMed ID: 20829353

Title: Structural basis for the cAMP-dependent gating in the human HCN4 channel.

PubMed ID: 20829353

DOI: 10.1074/jbc.m110.152033

PubMed ID: 22006928

Title: Tetramerization dynamics of C-terminal domain underlies isoform-specific cAMP gating in hyperpolarization-activated cyclic nucleotide-gated channels.

PubMed ID: 22006928

DOI: 10.1074/jbc.m111.297606

PubMed ID: 23103389

Title: Local and global interpretations of a disease-causing mutation near the ligand entry path in hyperpolarization-activated cAMP-gated channel.

PubMed ID: 23103389

DOI: 10.1016/j.str.2012.09.017

PubMed ID: 15123648

Title: Functional characterization of a trafficking-defective HCN4 mutation, D553N, associated with cardiac arrhythmia.

PubMed ID: 15123648

DOI: 10.1074/jbc.m311953200

PubMed ID: 16407510

Title: Familial sinus bradycardia associated with a mutation in the cardiac pacemaker channel.

PubMed ID: 16407510

DOI: 10.1056/nejmoa052475

PubMed ID: 20662977

Title: A novel mutation in the HCN4 gene causes symptomatic sinus bradycardia in Moroccan Jews.

PubMed ID: 20662977

DOI: 10.1111/j.1540-8167.2010.01844.x

PubMed ID: 30127718

Title: A loss-of-function HCN4 mutation associated with familial benign myoclonic epilepsy in infancy causes increased neuronal excitability.

PubMed ID: 30127718

DOI: 10.3389/fnmol.2018.00269

Sequence Information:

  • Length: 1203
  • Mass: 129042
  • Checksum: 7EFDD2D69CF1F9D9
  • Sequence:
  • MDKLPPSMRK RLYSLPQQVG AKAWIMDEEE DAEEEGAGGR QDPSRRSIRL RPLPSPSPSA 
    AAGGTESRSS ALGAADSEGP ARGAGKSSTN GDCRRFRGSL ASLGSRGGGS GGTGSGSSHG 
    HLHDSAEERR LIAEGDASPG EDRTPPGLAA EPERPGASAQ PAASPPPPQQ PPQPASASCE 
    QPSVDTAIKV EGGAAAGDQI LPEAEVRLGQ AGFMQRQFGA MLQPGVNKFS LRMFGSQKAV 
    EREQERVKSA GFWIIHPYSD FRFYWDLTML LLMVGNLIII PVGITFFKDE NTTPWIVFNV 
    VSDTFFLIDL VLNFRTGIVV EDNTEIILDP QRIKMKYLKS WFMVDFISSI PVDYIFLIVE 
    TRIDSEVYKT ARALRIVRFT KILSLLRLLR LSRLIRYIHQ WEEIFHMTYD LASAVVRIVN 
    LIGMMLLLCH WDGCLQFLVP MLQDFPDDCW VSINNMVNNS WGKQYSYALF KAMSHMLCIG 
    YGRQAPVGMS DVWLTMLSMI VGATCYAMFI GHATALIQSL DSSRRQYQEK YKQVEQYMSF 
    HKLPPDTRQR IHDYYEHRYQ GKMFDEESIL GELSEPLREE IINFNCRKLV ASMPLFANAD 
    PNFVTSMLTK LRFEVFQPGD YIIREGTIGK KMYFIQHGVV SVLTKGNKET KLADGSYFGE 
    ICLLTRGRRT ASVRADTYCR LYSLSVDNFN EVLEEYPMMR RAFETVALDR LDRIGKKNSI 
    LLHKVQHDLN SGVFNYQENE IIQQIVQHDR EMAHCAHRVQ AAASATPTPT PVIWTPLIQA 
    PLQAAAATTS VAIALTHHPR LPAAIFRPPP GSGLGNLGAG QTPRHLKRLQ SLIPSALGSA 
    SPASSPSQVD TPSSSSFHIQ QLAGFSAPAG LSPLLPSSSS SPPPGACGSP SAPTPSAGVA 
    ATTIAGFGHF HKALGGSLSS SDSPLLTPLQ PGARSPQAAQ PSPAPPGARG GLGLPEHFLP 
    PPPSSRSPSS SPGQLGQPPG ELSLGLATGP LSTPETPPRQ PEPPSLVAGA SGGASPVGFT 
    PRGGLSPPGH SPGPPRTFPS APPRASGSHG SLLLPPASSP PPPQVPQRRG TPPLTPGRLT 
    QDLKLISASQ PALPQDGAQT LRRASPHSSG ESMAAFPLFP RAGGGSGGSG SSGGLGPPGR 
    PYGAIPGQHV TLPRKTSSGS LPPPLSLFGA RATSSGGPPL TAGPQREPGA RPEPVRSKLP 
    SNL

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.