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HCN1

HCN1
Protein HCN1 PDB 1q3e.png
Available structures
PDB Ortholog search: PDBe RCSB
Identifiers
Aliases HCN1, BCNG-1, BCNG1, EIEE24, HAC-2, hyperpolarization activated cyclic nucleotide gated potassium channel 1
External IDs MGI: 1096392 HomoloGene: 32093 GeneCards: HCN1
Gene location (Human)
Chromosome 5 (human)
Chr. Chromosome 5 (human)
Chromosome 5 (human)
Genomic location for HCN1
Genomic location for HCN1
Band 5p12 Start 45,254,950 bp
End 45,696,498 bp
RNA expression pattern
PBB GE HCN1 gnf1h06726 at fs.png
More reference expression data
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_021072

NM_010408

RefSeq (protein)

NP_066550

NP_034538

Location (UCSC) Chr 5: 45.25 – 45.7 Mb Chr 5: 117.6 – 117.99 Mb
PubMed search

3U0Z

NM_021072

NM_010408

NP_066550

NP_034538

Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 1 is a protein that in humans is encoded by the HCN1 gene.

Hyperpolarization-activated cation channels of the HCN gene family, such as HCN1, contribute to spontaneous rhythmic activity in both heart and brain.

HCN1 channel expression is found in the sinoatrial node, the neocortex, hippocampus, cerebellar cortex, dorsal root ganglion, trigeminal ganglion and brainstem.

HCN1 has been shown to interact with HCN2.

De novo mutations in HCN1 cause epilepsy .

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


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