Neidio i'r cynnwys

DHX15

Ni chefnogir cynnwys y dudalen mewn ieithoedd eraill.

protein-coding gene in the species Homo sapiens

enghraifft o'r canlynol

isddosbarth o'r canlynol

genyn codio-protein[6]

found in taxon

amgodau

DEAH-box helicase 15[7]

genetic association

myopia[8]

dull penderfynu: genome-wide association study, TAS

cromosom

cromosom dynol 4[3]

cynulliad genynnol: genome assembly GRCh38, Genome assembly GRCh37

strand orientation

edefyn ôl[3]

cynulliad genynnol: genome assembly GRCh38, Genome assembly GRCh37

genomic start

24517441[3]

cromosom: cromosom dynol 4

cynulliad genynnol: genome assembly GRCh38

24519064[3]

cromosom: cromosom dynol 4

cynulliad genynnol: Genome assembly GRCh37

genomic end

24586173[3]

cromosom: cromosom dynol 4

cynulliad genynnol: Genome assembly GRCh37

24584554[3]

cromosom: cromosom dynol 4

cynulliad genynnol: genome assembly GRCh38

cytogenetic location

4p15.2[1]

HomoloGene ID

1040[1]

Gene Atlas image

ortholog

Dhx15[9][10]

found in taxon: Llygoden y tŷ

PRP43[9]

found in taxon: Saccharomyces cerevisiae S288c

Dhx15[9][10]

found in taxon: brown rat

Dhx15[9][10]

found in taxon: Drosophila melanogaster

dhx15[9]

found in taxon: Danio rerio

ddx-15[9][10]

found in taxon: Caenorhabditis elegans

expressed in

meinwe cartilag[11]

trefnolyn: 1

tibia[11]

trefnolyn: 2

germinal epithelium[11]

trefnolyn: 3

mucosa of sigmoid colon[11]

trefnolyn: 4

visceral pleura[11]

trefnolyn: 5

skin of hip[11]

trefnolyn: 6

parietal pleura[11]

trefnolyn: 7

embryo[11]

trefnolyn: 8

ventricular zone[11]

trefnolyn: 9

skin of thigh[11]

trefnolyn: 10

Cyfeiriadau

  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 Ebrill 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 Mehefin 2023, inferred by common HGNC mappings on source and on Wikidata
  5. Online Mendelian Inheritance in Man, 19 Awst 2019
  6. Ensembl Release 87, ENSG00000109606
  7. UniProt, 6 Gorffennaf 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 Mehefin 2024, https://www.bgee.org/gene/ENSG00000109606
  12. Identifiers.org, http://www.ebi.ac.uk/miriam/main/collections/MIR:00000069