Saltu al enhavo

DNM2

Paĝenhavo ne ekzistas en aliaj lingvoj.

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protein-coding gene in the species Homo sapiens

estas

subaro de

protein-kodanta geno[5]

en taksono

Homo sapiens[1]

kodas

Dynamin 2[6]
Dynamin-2[7]

rilato al geno

coronary artery disease[8]

determina metodo: tut-genara asociada studo, spurebla aŭtora aserto

fetal akinesia-cerebral and retinal hemorrhage syndrome[9][10]
Charcot-Marie-Tooth disease dominant intermediate B[11]

kromosomo

homa kromosomo 19[1]

genomic assembly: genome assembly GRCh38, Genome assembly GRCh37

orientiĝo de DNA-fadenoj

antaŭuma DNA-fadeno[1]

genomic assembly: genome assembly GRCh38, Genome assembly GRCh37

komenco de geno

10828755[1]

kromosomo: homa kromosomo 19

genomic assembly: Genome assembly GRCh37

10718055[1]

kromosomo: homa kromosomo 19

genomic assembly: genome assembly GRCh38

fino de geno

10833488[1]

kromosomo: homa kromosomo 19

genomic assembly: genome assembly GRCh38

10944164[1]

kromosomo: homa kromosomo 19

genomic assembly: Genome assembly GRCh37

ĉelgenetika loko

19p13.2[2]

HomoloGene ID

90883[2]

ortohomologa geno

Dnm2[12][13]

en taksono: hejma muso

Dnm2[12][13]

en taksono: Bruna rato

dnm2b[12]

en taksono: Danio rerio

esprimata en

Granulocito[14]

vicnumero: 1

mucosa of transverse colon[14]

vicnumero: 2

skin of leg[14]

vicnumero: 3

right lung[14]

vicnumero: 4

upper lobe of left lung[14]

vicnumero: 5

rektumo[14]

vicnumero: 6

skin of abdomen[14]

vicnumero: 7

body of stomach[14]

vicnumero: 8

apex of heart[14]

vicnumero: 9

gastric mucosa[14]

vicnumero: 10

Referenco

  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 1,21 1,22 1,23 1,24 1,25 1,26 1,27 1,28 1,29 1,30 1,31 1,32 1,33 1,34 ensembl Release 106, ENSG00000079805
  2. 2,00 2,01 2,02 2,03 2,04 2,05 2,06 2,07 2,08 2,09 NCBI Gene, 15 maj. 2022, 1785
  3. UMLS 2023, 15 jun. 2023, inferred by common HGNC mappings on source and on Wikidata
  4. Reta Mendela Heredo je Homoj, 19 aŭg. 2019
  5. Ensembl Release 87, ENSG00000079805
  6. UniProt, 6 jul. 2017, P50570
  7. K7EPK9, 30 jun. 2016, UniProt, angla lingvo
  8. Phenocarta, Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project, https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_3393&ncbiId=1785, http://www.genome.gov/gwastudies/index.cfm?gene=DNM2, 25 maj. 2020
  9. P50570, 13 aŭg. 2019, UniProt
  10. Open Targets Platform, 24 aŭg. 2023, https://platform.opentargets.org/evidence/ENSG00000079805/MONDO_0014149, inferred from an Open Targets association score over 0.7
  11. Open Targets Platform, 24 aŭg. 2023, https://platform.opentargets.org/evidence/ENSG00000079805/Orphanet_100044, inferred from an Open Targets association score over 0.7
  12. 12,0 12,1 12,2 HomoloGene build68, 90883
  13. 13,0 13,1 13,2 13,3 Orthologous MAtrix, https://omabrowser.org/oma/vps/P50570/
  14. 14,00 14,01 14,02 14,03 14,04 14,05 14,06 14,07 14,08 14,09 Bgee, 7 jun. 2024, https://www.bgee.org/gene/ENSG00000079805
  15. Identifiers.org, http://www.ebi.ac.uk/miriam/main/collections/MIR:00000069