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HCN2

From Wikipedia, the free encyclopedia
Protein-coding gene in the species Homo sapiens
HCN2
Available structures
PDBOrtholog search:PDBeRCSB
List of PDB id codes

2MPF,3U10

Identifiers
AliasesHCN2, BCNG-2, BCNG2, HAC-1, hyperpolarization activated cyclic nucleotide gated potassium channel 2, hyperpolarization activated cyclic nucleotide gated potassium and sodium channel 2, EIG17, FEB2, GEFSP11
External IDsOMIM:602781;MGI:1298210;HomoloGene:31022;GeneCards:HCN2;OMA:HCN2 - orthologs
Gene location (Human)
Chromosome 19 (human)
Chr.Chromosome 19 (human)[1]
Chromosome 19 (human)
Genomic location for HCN2
Genomic location for HCN2
Band19p13.3Start589,881bp[1]
End617,159bp[1]
Gene location (Mouse)
Chromosome 10 (mouse)
Chr.Chromosome 10 (mouse)[2]
Chromosome 10 (mouse)
Genomic location for HCN2
Genomic location for HCN2
Band10|10 C1Start79,552,468bp[2]
End79,571,942bp[2]
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • C1 segment

  • right frontal lobe

  • putamen

  • nucleus accumbens

  • anterior cingulate cortex

  • caudate nucleus

  • Brodmann area 10

  • Brodmann area 9

  • Amygdala

  • right hemisphere of cerebellum
Top expressed in
  • perirhinal cortex

  • entorhinal cortex

  • primary visual cortex

  • superior frontal gyrus

  • CA3 field

  • choroid plexus of fourth ventricle

  • central gray substance of midbrain

  • cerebellar cortex

  • Medulla Oblongata

  • lumbar subsegment of spinal cord
More reference expression data
BioGPS


More reference expression data
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo /QuickGO
Orthologs
SpeciesHumanMouse
Entrez

610

15166

Ensembl

ENSG00000099822

ENSMUSG00000020331

UniProt

Q9UL51

O88703

RefSeq (mRNA)

NM_001194

NM_008226

RefSeq (protein)

NP_001185

NP_032252

Location (UCSC)Chr 19: 0.59 – 0.62 MbChr 10: 79.55 – 79.57 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated ion channel 2 is aprotein that in humans is encoded by theHCN2gene.[5][6][7][8]

Interactions

[edit]

HCN2 has been shown tointeract withHCN1[9][10] andHCN4.[9]

Function

[edit]

The function of the channel is not known although its activation by hyperpolarization alludes to thefunny channels in thesinoatrial node of the heart (which form the basis of spontaneous generation of electrical rhythm). These channels have recently been associated with chronic pain and blocking the gene is associated with resolution of neuropathic episodes ofpain.[11]

See also

[edit]

References

[edit]
  1. ^abcGRCh38: Ensembl release 89: ENSG00000099822Ensembl, May 2017
  2. ^abcGRCm38: Ensembl release 89: ENSMUSG00000020331Ensembl, May 2017
  3. ^"Human PubMed Reference:".National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^"Mouse PubMed Reference:".National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^Santoro B, Grant SG, Bartsch D, Kandel ER (Dec 1997)."Interactive cloning with the SH3 domain of N-src identifies a new brain specific ion channel protein, with homology to eag and cyclic nucleotide-gated channels".Proceedings of the National Academy of Sciences of the United States of America.94 (26):14815–20.Bibcode:1997PNAS...9414815S.doi:10.1073/pnas.94.26.14815.PMC 25120.PMID 9405696.
  6. ^Santoro B, Liu DT, Yao H, Bartsch D, Kandel ER, Siegelbaum SA, Tibbs GR (May 1998)."Identification of a gene encoding a hyperpolarization-activated pacemaker channel of brain".Cell.93 (5):717–29.doi:10.1016/S0092-8674(00)81434-8.PMID 9630217.S2CID 10265917.
  7. ^Hofmann F, Biel M, Kaupp UB (Dec 2005). "International Union of Pharmacology. LI. Nomenclature and structure-function relationships of cyclic nucleotide-regulated channels".Pharmacological Reviews.57 (4):455–62.doi:10.1124/pr.57.4.8.PMID 16382102.S2CID 45853869.
  8. ^"Entrez Gene: HCN2 hyperpolarization activated cyclic nucleotide-gated potassium channel 2".
  9. ^abMuch B, Wahl-Schott C, Zong X, Schneider A, Baumann L, Moosmang S, Ludwig A, Biel M (Oct 2003)."Role of subunit heteromerization and N-linked glycosylation in the formation of functional hyperpolarization-activated cyclic nucleotide-gated channels".The Journal of Biological Chemistry.278 (44):43781–6.doi:10.1074/jbc.M306958200.PMID 12928435.
  10. ^Proenza C, Tran N, Angoli D, Zahynacz K, Balcar P, Accili EA (Aug 2002)."Different roles for the cyclic nucleotide binding domain and amino terminus in assembly and expression of hyperpolarization-activated, cyclic nucleotide-gated channels".The Journal of Biological Chemistry.277 (33):29634–42.doi:10.1074/jbc.M200504200.PMID 12034718.
  11. ^"Gene find may lead to pills that kill chronic pain".The Times of India. 10 September 2011. Archived fromthe original on 6 November 2012.

Further reading

[edit]

External links

[edit]

This article incorporates text from theUnited States National Library of Medicine, which is in thepublic domain.

PDB gallery
  • 1q3e: HCN2J 443-645 in the presence of cGMP
    1q3e: HCN2J 443-645 in the presence of cGMP
  • 1q43: HCN2I 443-640 in the presence of cAMP, selenomethionine derivative
    1q43: HCN2I 443-640 in the presence of cAMP, selenomethionine derivative
  • 1q5o: HCN2J 443-645 in the presence of cAMP, selenomethionine derivative
    1q5o: HCN2J 443-645 in the presence of cAMP, selenomethionine derivative
Ligand-gated
Voltage-gated
Constitutively active
Proton-gated
Voltage-gated
Calcium-activated
Inward-rectifier
Tandem pore domain
Voltage-gated
Miscellaneous
Cl:Chloride channel
H+:Proton channel
M+:CNG cation channel
M+:TRP cation channel
H2O (+solutes):Porin
Cytoplasm:Gap junction
By gating mechanism
Ion channel class
see alsodisorders


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