KCND1

Protein-coding gene in the species Homo sapiens
KCND1
Identifiers
AliasesKCND1, KV4.1, potassium voltage-gated channel subfamily D member 1
External IDsOMIM: 300281 MGI: 96671 HomoloGene: 21035 GeneCards: KCND1
Gene location (Human)
X chromosome (human)
Chr.X chromosome (human)[1]
X chromosome (human)
Genomic location for KCND1
Genomic location for KCND1
BandXp11.23Start48,961,378 bp[1]
End48,971,844 bp[1]
Gene location (Mouse)
X chromosome (mouse)
Chr.X chromosome (mouse)[2]
X chromosome (mouse)
Genomic location for KCND1
Genomic location for KCND1
BandX A1.1|X 3.53 cMStart7,688,528 bp[2]
End7,704,519 bp[2]
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • left uterine tube

  • stromal cell of endometrium

  • ascending aorta

  • left coronary artery

  • gallbladder

  • smooth muscle tissue

  • right coronary artery

  • gastric mucosa

  • prefrontal cortex

  • cerebellar vermis
Top expressed in
  • facial motor nucleus

  • anterior horn of spinal cord

  • superior frontal gyrus

  • trigeminal ganglion

  • calvaria

  • submandibular gland

  • neural tube

  • cerebellar cortex

  • renal corpuscle

  • yolk sac
More reference expression data
BioGPS
More reference expression data
Gene ontology
Molecular function
  • potassium channel activity
  • metal ion binding
  • voltage-gated ion channel activity
  • ion channel activity
  • A-type (transient outward) potassium channel activity
  • voltage-gated potassium channel activity
Cellular component
  • integral component of membrane
  • cell projection
  • membrane
  • voltage-gated potassium channel complex
  • plasma membrane
  • neuronal cell body
  • dendrite
  • cellular component
Biological process
  • regulation of ion transmembrane transport
  • ion transport
  • potassium ion transport
  • transmembrane transport
  • potassium ion transmembrane transport
  • protein homooligomerization
  • cardiac conduction
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

3750

16506

Ensembl

ENSG00000102057

ENSMUSG00000009731

UniProt

Q9NSA2

Q03719

RefSeq (mRNA)

NM_004979

NM_008423

RefSeq (protein)

NP_004970

NP_032449

Location (UCSC)Chr X: 48.96 – 48.97 MbChr X: 7.69 – 7.7 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Potassium voltage-gated channel, Shal-related subfamily, member 1 (KCND1), also known as Kv4.1, is a human gene.[5]

Voltage-gated potassium (Kv) channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. Four sequence-related potassium channel genes - shaker, shaw, shab, and shal - have been identified in Drosophila, and each has been shown to have human homolog(s). This gene encodes a member of the potassium channel, voltage-gated, shal-related subfamily, members of which form voltage-activated A-type potassium ion channels and are prominent in the repolarization phase of the action potential. This gene is expressed at moderate levels in all tissues analyzed, with lower levels in skeletal muscle.[5]

See also

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000102057 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000009731 – Ensembl, 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. ^ a b "Entrez Gene: KCND1 potassium voltage-gated channel, Shal-related subfamily, member 1".

Further reading

  • Gutman GA, Chandy KG, Grissmer S, et al. (2006). "International Union of Pharmacology. LIII. Nomenclature and molecular relationships of voltage-gated potassium channels". Pharmacol. Rev. 57 (4): 473–508. doi:10.1124/pr.57.4.10. PMID 16382104. S2CID 219195192.
  • Kurschner C, Yuzaki M (1999). "Neuronal interleukin-16 (NIL-16): a dual function PDZ domain protein". J. Neurosci. 19 (18): 7770–80. doi:10.1523/JNEUROSCI.19-18-07770.1999. PMC 6782450. PMID 10479680.
  • Isbrandt D, Leicher T, Waldschütz R, et al. (2000). "Gene structures and expression profiles of three human KCND (Kv4) potassium channels mediating A-type currents I(TO) and I(SA)". Genomics. 64 (2): 144–54. doi:10.1006/geno.2000.6117. PMID 10729221.
  • Nakamura TY, Nandi S, Pountney DJ, et al. (2001). "Different effects of the Ca(2+)-binding protein, KChIP1, on two Kv4 subfamily members, Kv4.1 and Kv4.2". FEBS Lett. 499 (3): 205–9. doi:10.1016/S0014-5793(01)02560-1. PMID 11423117.
  • Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. Bibcode:2002PNAS...9916899M. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
  • Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039.
  • Jerng HH, Qian Y, Pfaffinger PJ (2005). "Modulation of Kv4.2 channel expression and gating by dipeptidyl peptidase 10 (DPP10)". Biophys. J. 87 (4): 2380–96. doi:10.1529/biophysj.104.042358. PMC 1304660. PMID 15454437.
  • Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
  • Kim SJ, Choi WS, Han JS, et al. (2005). "A novel mechanism for the suppression of a voltage-gated potassium channel by glucose-dependent insulinotropic polypeptide: protein kinase A-dependent endocytosis". J. Biol. Chem. 280 (31): 28692–700. doi:10.1074/jbc.M504913200. PMID 15955806.

This article incorporates text from the United States National Library of Medicine, which is in the public domain.

  • v
  • t
  • e
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 also disorders


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