DNMT3B
protein-coding gene in the species Homo sapiens
mille alamklass
protein-coding gene[6]
found in taxon
Homo sapiens[1]
encodes
DNA methyltransferase 3 beta[7]
genetic association
immunodeficiency-centromeric instability-facial anomalies syndrome[9]
chromosome
strand orientation
genomic start
genomic end
cytogenetic location
20q11.21[2]
HomoloGene ID
56000[2]
Gene Atlas image
ortholog
expressed in
täpne vaste
Viited
- ↑ 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 ensembl Release 105, ENSG00000088305
- ↑ 2,00 2,01 2,02 2,03 2,04 2,05 2,06 2,07 2,08 2,09 2,10 2,11 2,12 2,13 2,14 2,15 NCBI Gene, 9. jaanuar 2022, 1789
- ↑ UMLS 2023, 15. juuni 2023, inferred by common HGNC mappings on source and on Wikidata
- ↑ Online Mendelian Inheritance in Man, 19. august 2019
- ↑ OpenAlex, 26. jaanuar 2022, https://docs.openalex.org/download-snapshot/snapshot-data-format
- ↑ Ensembl Release 87, ENSG00000088305
- ↑ UniProt, 6. juuli 2017, Q9UBC3
- ↑ Phenocarta, Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease, https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_0050589&ncbiId=1789, http://www.genome.gov/gwastudies/index.cfm?gene=DNMT3B, 25. mai 2020
- ↑ Open Targets Platform, 24. august 2023, https://platform.opentargets.org/evidence/ENSG00000088305/Orphanet_2268, inferred from an Open Targets association score over 0.7
- ↑ 10,0 10,1 10,2 HomoloGene build68, 56000
- ↑ 11,0 11,1 Orthologous MAtrix, https://omabrowser.org/oma/vps/Q9UBC3/
- ↑ 12,00 12,01 12,02 12,03 12,04 12,05 12,06 12,07 12,08 12,09 Bgee, 7. juuni 2024, https://www.bgee.org/gene/ENSG00000088305
- ↑ Identifiers.org, http://www.ebi.ac.uk/miriam/main/collections/MIR:00000069