HCN1
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 5[12]
- Cytogenetic location
- 5p12[16]
- Expressed in
- endothelial cell, Brodmann area 23, primary visual cortex, trigeminal ganglion, Brodmann area 46, spinal ganglia, prefrontal cortex, superior frontal gyrus, middle temporal gyrus, parietal lobe[17][18][19][20][21][22][23][24][25][26]
- Found in taxon
- Homo sapiens[11]
- Genetic association
- undetermined early-onset epileptic encephalopathy, generalized epilepsy with febrile seizures plus[13][14]
- HomoloGene ID
- 32093[3]
- Strand orientation
- reverse strand[15]
🏷️ Also known as
en BCNG-1
en BCNG1
en DEE24
en EIEE24
en GEFSP10
en HAC-2
en HCN1
en hyperpolarization activated cyclic nucleotide gated potassium channel 1
🔖 Identifiers · 11
- Image (Wikimedia Commons)
- 5u6p.jpg ↗
- Ensembl gene ID
- ENSG00000164588
- Ensembl transcript ID
- ENST00000303230, ENST00000634658, ENST00000637256, ENST00000637305, ENST00000638054, ENST00000673735
- Entrez Gene ID
- 348980
- Exact match
- identifiers.org
- Freebase ID
- /m/03h05vq
- HGNC ID
- 4845
- HGNC gene symbol
- HCN1
- OMIM ID
- 602780
- RefSeq RNA ID
- NM_021072
- UMLS CUI
- C1415498
🔗 Connections
Expressed in 7
Chromosome 1
Found in taxon 1
Instance of 1
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