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DNMT1

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protein-coding gene in the species Homo sapiens

Välised allikad

Microsoft Academic ID
175211621
Ensembl transcript ID
ENST00000593049[1]
ENST00000340748[1]
ENST00000359526[1]
ENST00000585843[1]
ENST00000585920[1]
ENST00000586086[1]
ENST00000586588[1]
ENST00000586667[1]
ENST00000586799[1]
ENST00000586800[1]
ENST00000586988[1]
ENST00000587197[1]
ENST00000587604[1]
ENST00000588118[1]
ENST00000588913[1]
ENST00000588952[1]
ENST00000589091[1]
ENST00000589294[1]
ENST00000589349[1]
ENST00000589351[1]
ENST00000589538[1]
ENST00000590619[1]
ENST00000591239[1]
ENST00000591764[1]
ENST00000591798[1]
ENST00000592054[1]
ENST00000592342[1]
ENST00000592705[1]
ENST00000678694[1]
ENST00000677135[1]
ENST00000679313[1]
ENST00000677634[1]
ENST00000678239[1]
ENST00000678957[1]
ENST00000677783[1]
ENST00000677013[1]
ENST00000678647[1]
ENST00000676820[1]
ENST00000677685[1]
ENST00000678024[1]
ENST00000679100[1]
ENST00000677250[1]
ENST00000678107[1]
ENST00000677038[1]
ENST00000679103[1]
ENST00000677616[1]
ENST00000678851[1]
ENST00000678804[1]
ENST00000676610[1]
ENST00000677946[1]
ENST00000676868[1]
ENST00000676604[1]
Entrez Gene ID
1786[2]
RefSeq RNA ID
NM_001130823[2]
NM_001379[2]
NM_001318730[2]
NM_001318731[2]
Ensembl gene ID
ENSG00000130816[1]
Freebase
/m/03bxt95
UMLS CUI
C1414121[3]
CIViC gene ID
1510
OpenAlex ID
C175211621[4]
OMIM ID
126375[5]
HGNC ID
2976[2]
HGNC gene symbol
DNMT1[2]

üksikjuht nähtusest

geen[1]

mille alamklass

protein-coding gene[6]

found in taxon

Homo sapiens[1]

encodes

DNA methyltransferase 1[7][8]

genetic association

hereditary sensory neuropathy-deafness-dementia syndrome[9][10]
autosomal dominant cerebellar ataxia, deafness and narcolepsy[9][11][12][13]

chromosome

human chromosome 19[1]

genomic assembly: genome assembly GRCh38, Genome assembly GRCh37

strand orientation

reverse strand[1]

genomic assembly: genome assembly GRCh38, Genome assembly GRCh37

genomic start

10244021[1]

chromosome: human chromosome 19

genomic assembly: Genome assembly GRCh37

10133342[1]

chromosome: human chromosome 19

genomic assembly: genome assembly GRCh38

genomic end

10231286[1]

chromosome: human chromosome 19

genomic assembly: genome assembly GRCh38

10341962[1]

chromosome: human chromosome 19

genomic assembly: Genome assembly GRCh37

cytogenetic location

19p13.2[2]

HomoloGene ID

124071[2]

Gene Atlas image

ortholog

Dnmt1[14][15]

found in taxon: koduhiir

Dnmt1[14][15]

found in taxon: rändrott

dnmt1[14][15]

found in taxon: Danio rerio

expressed in

ootsüüt[16]

järjekorranumber: 1

secondary oocyte[16]

järjekorranumber: 2

sural nerve[16]

järjekorranumber: 3

ventricular zone[16]

järjekorranumber: 4

ganglionic eminence[16]

järjekorranumber: 5

bone marrow cells[16]

järjekorranumber: 6

Ussripik[16]

järjekorranumber: 7

cerebellar hemisphere[16]

järjekorranumber: 8

right hemisphere of cerebellum[16]

järjekorranumber: 9

Achilleuse kõõlus[16]

järjekorranumber: 10

täpne vaste

http://identifiers.org/ncbigene/1786[17]

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 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 1,35 1,36 1,37 1,38 1,39 1,40 1,41 1,42 1,43 1,44 1,45 1,46 1,47 1,48 1,49 1,50 1,51 1,52 1,53 1,54 1,55 1,56 1,57 1,58 1,59 1,60 ensembl Release 106, ENSG00000130816
  2. ↑ 2,0 2,1 2,2 2,3 2,4 2,5 2,6 2,7 2,8 NCBI Gene, 15. mai 2022, 1786
  3. ↑ UMLS 2023, 15. juuni 2023, inferred by common HGNC mappings on source and on Wikidata
  4. ↑ OpenAlex, 26. jaanuar 2022, https://docs.openalex.org/download-snapshot/snapshot-data-format
  5. ↑ Online Mendelian Inheritance in Man, 19. august 2019
  6. ↑ Ensembl Release 87, ENSG00000130816
  7. ↑ UniProt, 6. juuli 2017, P26358
  8. ↑ K7ELB1, 21. märts 2016, UniProt, inglise keel
  9. ↑ 9,0 9,1 P26358, 13. august 2019, UniProt
  10. ↑ Open Targets Platform, 24. august 2023, https://platform.opentargets.org/evidence/ENSG00000130816/MONDO_0013584, inferred from an Open Targets association score over 0.7
  11. ↑ ClinGen, 8. detsember 2020, https://search.clinicalgenome.org/kb/gene-validity/6235
  12. ↑ ClinGen, 25. jaanuar 2022, https://search.clinicalgenome.org/kb/gene-validity/CGGCIEX:assertion_6235
  13. ↑ Open Targets Platform, 24. august 2023, https://platform.opentargets.org/evidence/ENSG00000130816/MONDO_0011397, inferred from an Open Targets association score over 0.7
  14. ↑ 14,0 14,1 14,2 HomoloGene build68, 124071
  15. ↑ 15,0 15,1 15,2 Orthologous MAtrix, https://omabrowser.org/oma/vps/P26358/
  16. ↑ 16,00 16,01 16,02 16,03 16,04 16,05 16,06 16,07 16,08 16,09 Bgee, 7. juuni 2024, https://www.bgee.org/gene/ENSG00000130816
  17. ↑ Identifiers.org, http://www.ebi.ac.uk/miriam/main/collections/MIR:00000069
Pärit leheküljelt "https://et.wikipedia.org/wiki/Eri:AboutTopic/Q14907998"