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HVCN1

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protein-coding gene in the species Homo sapiens

Välised allikad

RefSeq RNA ID
NM_001040107[1]
NM_001256413[1]
NM_032369[1]
XM_005253948[1]
XM_011538838[1]
XM_011538839[1]
XM_011538840[1]
XM_011538841[1]
XM_011538842[1]
XM_011538844[1]
XM_011538845[1]
XM_011538846[1]
XM_011538847[1]
XM_017020026[1]
XM_017020027[1]
XM_024449225[1]
XM_047429669[2]
XM_047429670[2]
Ensembl transcript ID
ENST00000620084[3]
ENST00000242607[3]
ENST00000356742[3]
ENST00000439744[3]
ENST00000546425[3]
ENST00000546713[3]
ENST00000547887[3]
ENST00000548312[3]
ENST00000549442[3]
Entrez Gene ID
84329[1]
UMLS CUI
C1825554[4]
OMIM ID
611227[5]
Ensembl gene ID
ENSG00000122986[3]
HGNC ID
28240[1]
HGNC gene symbol
HVCN1[1]
Freebase
/m/0h6501b

üksikjuht nähtusest

geen[3]

mille alamklass

protein-coding gene[6]

found in taxon

Homo sapiens[3]

encodes

Hydrogen voltage gated channel 1[7]

chromosome

human chromosome 12[3]

genomic assembly: genome assembly GRCh38, Genome assembly GRCh37

strand orientation

reverse strand[3]

genomic assembly: genome assembly GRCh38, Genome assembly GRCh37

genomic start

110627841[3]

chromosome: human chromosome 12

genomic assembly: genome assembly GRCh38

111065646[3]

chromosome: human chromosome 12

genomic assembly: Genome assembly GRCh37

genomic end

110704950[3]

chromosome: human chromosome 12

genomic assembly: genome assembly GRCh38

111142755[3]

chromosome: human chromosome 12

genomic assembly: Genome assembly GRCh37

cytogenetic location

12q24.11[1]

HomoloGene ID

12535[1]

ortholog

Hvcn1[8][9]

found in taxon: koduhiir

Hvcn1[8][9]

found in taxon: rändrott

hvcn1[8][9]

found in taxon: Danio rerio

expressed in

Leukotsüüt[10]

järjekorranumber: 1

monotsüüt[10]

järjekorranumber: 2

granulocyte[10]

järjekorranumber: 3

lümfisõlm[10]

järjekorranumber: 4

mucosa of ileum[10]

järjekorranumber: 5

veri[10]

järjekorranumber: 6

left testis[10]

järjekorranumber: 7

põrn[10]

järjekorranumber: 8

right testis[10]

järjekorranumber: 9

Ussripik[10]

järjekorranumber: 10

täpne vaste

http://identifiers.org/ncbigene/84329[11]

Viited

  1. ↑ 1,00 1,01 1,02 1,03 1,04 1,05 1,06 1,07 1,08 1,09 1,10 1,11 1,12 1,13 1,14 1,15 1,16 1,17 1,18 1,19 1,20 NCBI Gene, 15. mai 2022, 84329
  2. ↑ 2,0 2,1 NCBI Gene, 10. aprill 2022, 84329
  3. ↑ 3,00 3,01 3,02 3,03 3,04 3,05 3,06 3,07 3,08 3,09 3,10 3,11 3,12 3,13 3,14 3,15 3,16 3,17 ensembl Release 106, ENSG00000122986
  4. ↑ UMLS 2023, 15. juuni 2023, inferred by common HGNC mappings on source and on Wikidata
  5. ↑ Online Mendelian Inheritance in Man, 19. august 2019
  6. ↑ Ensembl Release 87, ENSG00000122986
  7. ↑ UniProt, 6. juuli 2017, Q96D96
  8. ↑ 8,0 8,1 8,2 HomoloGene build68, 12535
  9. ↑ 9,0 9,1 9,2 Orthologous MAtrix, https://omabrowser.org/oma/vps/Q96D96/
  10. ↑ 10,00 10,01 10,02 10,03 10,04 10,05 10,06 10,07 10,08 10,09 Bgee, 7. juuni 2024, https://www.bgee.org/gene/ENSG00000122986
  11. ↑ Identifiers.org, http://www.ebi.ac.uk/miriam/main/collections/MIR:00000069
Pärit leheküljelt "https://et.wikipedia.org/wiki/Eri:AboutTopic/Q18047575"