લખાણ પર જાઓ

SETD2

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protein-coding gene in the species Homo sapiens

બાહ્ય સ્રોતો

ફ્રીબેઝ આઈડી
/m/03h057g
Microsoft Academic ID
178658977
Ensembl transcript ID
ENST00000492397[૧]
ENST00000330022[૧]
ENST00000409792[૧]
ENST00000412450[૧]
ENST00000431180[૧]
ENST00000445387[૧]
ENST00000479832[૧]
ENST00000484689[૧]
ENST00000638947[૧]
Entrez Gene ID
29072[૨]
Ensembl gene ID
ENSG00000181555[૧]
UMLS CUI
C1822686[૩]
HGNC gene symbol
SETD2[૨]
OMIM ID
612778[૪]
HGNC ID
18420[૨]
RefSeq RNA ID
NM_012271[૨]
NM_014159[૨]
XM_011533631[૨]
XM_011533632[૨]
XM_011533633[૨]
XM_011533634[૨]
XR_940418[૨]
XM_017006270[૨]
XR_001740125[૨]
XR_001740126[૨]
XR_001740127[૨]
XR_001740128[૨]
XR_001740129[૨]
XR_001740130[૨]
XR_001740131[૨]
XR_001740132[૨]
XR_001740133[૨]
NM_001349370[૨]
NR_146158[૨]

ઉદાહરણ

gene[૧]

નો પેટા-પ્રકાર

protein-coding gene[૫]

found in taxon

Homo sapiens[૧]

encodes

SET domain containing 2, histone lysine methyltransferase[૬]

genetic association

nonpapillary renal cell carcinoma[૭]
acute myeloid leukemia[૭]
Luscan-Lumish syndrome[૮]

chromosome

human chromosome 3[૧]

genomic assembly: genome assembly GRCh38, Genome assembly GRCh37

strand orientation

reverse strand[૧]

genomic assembly: genome assembly GRCh38, Genome assembly GRCh37

genomic start

47016429[૧]

chromosome: human chromosome 3

genomic assembly: genome assembly GRCh38

47057919[૧]

chromosome: human chromosome 3

genomic assembly: Genome assembly GRCh37

genomic end

47163967[૧]

chromosome: human chromosome 3

genomic assembly: genome assembly GRCh38

47205457[૧]

chromosome: human chromosome 3

genomic assembly: Genome assembly GRCh37

cytogenetic location

3p21.31[૨]

HomoloGene ID

56493[૨]

Gene Atlas image

ortholog

Setd2[૯][૧૦]

found in taxon: ઘર ઉંદર

Setd2[૯]

found in taxon: brown rat

setd2[૯]

found in taxon: Danio rerio

expressed in

tendon of biceps brachii[૧૧]

series ordinal: 1

endothelial cell[૧૧]

series ordinal: 2

epithelium of colon[૧૧]

series ordinal: 3

Achilles tendon[૧૧]

series ordinal: 4

ventricular zone[૧૧]

series ordinal: 5

sural nerve[૧૧]

series ordinal: 6

pancreatic ductal cell[૧૧]

series ordinal: 7

ganglionic eminence[૧૧]

series ordinal: 8

internal globus pallidus[૧૧]

series ordinal: 9

tonsil[૧૧]

series ordinal: 10

exact match

http://identifiers.org/ncbigene/29072[૧૨]

સંદર્ભ

  1. ↑ ૧.૦૦ ૧.૦૧ ૧.૦૨ ૧.૦૩ ૧.૦૪ ૧.૦૫ ૧.૦૬ ૧.૦૭ ૧.૦૮ ૧.૦૯ ૧.૧૦ ૧.૧૧ ૧.૧૨ ૧.૧૩ ૧.૧૪ ૧.૧૫ ૧.૧૬ ૧.૧૭ Ensembl Release 91, ENSG00000181555
  2. ↑ ૨.૦૦ ૨.૦૧ ૨.૦૨ ૨.૦૩ ૨.૦૪ ૨.૦૫ ૨.૦૬ ૨.૦૭ ૨.૦૮ ૨.૦૯ ૨.૧૦ ૨.૧૧ ૨.૧૨ ૨.૧૩ ૨.૧૪ ૨.૧૫ ૨.૧૬ ૨.૧૭ ૨.૧૮ ૨.૧૯ ૨.૨૦ ૨.૨૧ ૨.૨૨ ૨.૨૩ NCBI Gene, ૧૧ નવેમ્બર 2017, 29072
  3. ↑ UMLS 2023, ૧૫ જૂન 2023, inferred by common HGNC mappings on source and on Wikidata
  4. ↑ Online Mendelian Inheritance in Man, ૧૯ ઓગસ્ટ 2019
  5. ↑ Ensembl Release 87, ENSG00000181555
  6. ↑ UniProt, ૬ જુલાઇ 2017, Q9BYW2
  7. ↑ ૭.૦ ૭.૧ Q9BYW2, ૧૩ ઓગસ્ટ 2019, UniProt
  8. ↑ Open Targets Platform, ૨૪ ઓગસ્ટ 2023, https://platform.opentargets.org/evidence/ENSG00000181555/MONDO_0014791, inferred from an Open Targets association score over 0.7
  9. ↑ ૯.૦ ૯.૧ ૯.૨ HomoloGene build68, 56493
  10. ↑ Orthologous MAtrix, https://omabrowser.org/oma/vps/Q9BYW2/
  11. ↑ ૧૧.૦૦ ૧૧.૦૧ ૧૧.૦૨ ૧૧.૦૩ ૧૧.૦૪ ૧૧.૦૫ ૧૧.૦૬ ૧૧.૦૭ ૧૧.૦૮ ૧૧.૦૯ Bgee, ૭ જૂન 2024, https://www.bgee.org/gene/ENSG00000181555
  12. ↑ Identifiers.org, http://www.ebi.ac.uk/miriam/main/collections/MIR:00000069
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