DHX15

protein-coding gene in the species Homo sapiens

üksikjuht nähtusest

mille alamklass

protein-coding gene[6]

found in taxon

Homo sapiens[3]

encodes

DEAH-box helicase 15[7]

genetic association

chromosome

human chromosome 4[3]

genomic assembly: genome assembly GRCh38, Genome assembly GRCh37

strand orientation

reverse strand[3]

genomic assembly: genome assembly GRCh38, Genome assembly GRCh37

genomic start

24517441[3]

chromosome: human chromosome 4

genomic assembly: genome assembly GRCh38

24519064[3]

chromosome: human chromosome 4

genomic assembly: Genome assembly GRCh37

genomic end

24586173[3]

chromosome: human chromosome 4

genomic assembly: Genome assembly GRCh37

24584554[3]

chromosome: human chromosome 4

genomic assembly: genome assembly GRCh38

cytogenetic location

4p15.2[1]

HomoloGene ID

1040[1]

Gene Atlas image

ortholog

Dhx15[9][10]

found in taxon: koduhiir

PRP43[9]

found in taxon: Saccharomyces cerevisiae S288c

Dhx15[9][10]

found in taxon: rändrott

Dhx15[9][10]

found in taxon: Harilik äädikakärbes

dhx15[9]

found in taxon: Danio rerio

ddx-15[9][10]

found in taxon: varbuss

expressed in

cartilage tissue[11]

järjekorranumber: 1

sääreluu[11]

järjekorranumber: 2

germinal epithelium[11]

järjekorranumber: 3

mucosa of sigmoid colon[11]

järjekorranumber: 4

visceral pleura[11]

järjekorranumber: 5

skin of hip[11]

järjekorranumber: 6

parietal pleura[11]

järjekorranumber: 7

embrüo[11]

järjekorranumber: 8

ventricular zone[11]

järjekorranumber: 9

skin of thigh[11]

järjekorranumber: 10

Viited

  1. 1,0 1,1 1,2 1,3 1,4 1,5 NCBI Gene, 15. mai 2022, 1665
  2. 2,0 2,1 NCBI Gene, 10. aprill 2022, 1665
  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 3,18 ensembl Release 106, ENSG00000109606
  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, ENSG00000109606
  7. UniProt, 6. juuli 2017, O43143
  8. Phenocarta, A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population, https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11830&ncbiId=1665, http://www.genome.gov/gwastudies/index.cfm?gene=DHX15, 25. mai 2020
  9. 9,0 9,1 9,2 9,3 9,4 9,5 HomoloGene build68, 1040
  10. 10,0 10,1 10,2 10,3 Orthologous MAtrix, https://omabrowser.org/oma/vps/O43143/
  11. 11,00 11,01 11,02 11,03 11,04 11,05 11,06 11,07 11,08 11,09 Bgee, 7. juuni 2024, https://www.bgee.org/gene/ENSG00000109606
  12. Identifiers.org, http://www.ebi.ac.uk/miriam/main/collections/MIR:00000069