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IKZF3

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protein-coding gene in the species Homo sapiens

Välised allikad

RefSeq RNA ID
NM_183232[1]
NM_001257408[1]
NM_001257409[1]
NM_001257410[1]
NM_001257411[1]
NM_001257412[1]
NM_001257413[1]
NM_001257414[1]
NM_001284514[1]
NM_001284515[1]
NM_001284516[1]
NM_012481[1]
NM_183228[1]
NM_183229[1]
NM_183230[1]
NM_183231[1]
XM_047435625[2]
Microsoft Academic ID
2779480474
Ensembl transcript ID
ENST00000623724[3]
ENST00000293068[3]
ENST00000346243[3]
ENST00000346872[3]
ENST00000348427[3]
ENST00000350532[3]
ENST00000351680[3]
ENST00000377944[3]
ENST00000377945[3]
ENST00000377952[3]
ENST00000377958[3]
ENST00000394189[3]
ENST00000439016[3]
ENST00000439167[3]
ENST00000467757[3]
ENST00000535189[3]
ENST00000583368[3]
Entrez Gene ID
22806[1]
UMLS CUI
C1825590[4]
Ensembl gene ID
ENSG00000161405[3]
OMIM ID
606221[5]
HGNC ID
13178[1]
HGNC gene symbol
IKZF3[1]
Freebase
/m/03gyg9n

üksikjuht nähtusest

geen[3]

mille alamklass

protein-coding gene[6]

found in taxon

Homo sapiens[3]

encodes

IKAROS family zinc finger 3[7]

genetic association

primary biliary cholangitis[8]

määramismeetod: Ülegenoomne assotsiatsiooniuuring, TAS

chromosome

human chromosome 17[3]

genomic assembly: genome assembly GRCh38, Genome assembly GRCh37

strand orientation

reverse strand[3]

genomic assembly: genome assembly GRCh38, Genome assembly GRCh37

genomic start

37921198[3]

chromosome: human chromosome 17

genomic assembly: Genome assembly GRCh37

39757718[3]

chromosome: human chromosome 17

genomic assembly: genome assembly GRCh38

genomic end

38020441[3]

chromosome: human chromosome 17

genomic assembly: Genome assembly GRCh37

39864312[3]

chromosome: human chromosome 17

genomic assembly: genome assembly GRCh38

cytogenetic location

17q12-q21.1[1]

HomoloGene ID

8269[1]

Gene Atlas image

ortholog

Ikzf3[9][10]

found in taxon: koduhiir

Ikzf3[9][10]

found in taxon: rändrott

expressed in

granulocyte[11]

järjekorranumber: 1

lümfisõlm[11]

järjekorranumber: 2

epithelium of nasopharynx[11]

järjekorranumber: 3

bone marrow cells[11]

järjekorranumber: 4

Tüümus[11]

järjekorranumber: 5

põrn[11]

järjekorranumber: 6

veri[11]

järjekorranumber: 7

Mandlid[11]

järjekorranumber: 8

superficial temporal artery[11]

järjekorranumber: 9

Ussripik[11]

järjekorranumber: 10

täpne vaste

http://identifiers.org/ncbigene/22806[12]

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 NCBI Gene, 15. mai 2022, 22806
  2. ↑ NCBI Gene, 10. aprill 2022, 22806
  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 3,19 3,20 3,21 3,22 3,23 3,24 3,25 ensembl Release 106, ENSG00000161405
  4. ↑ UMLS 2023, 15. juuni 2023, inferred by common HGNC mappings on source and on Wikidata
  5. ↑ Online Mendelian Inheritance in Man, 19. august 2019
  6. ↑ Ensembl Release 87, ENSG00000161405
  7. ↑ UniProt, 6. juuli 2017, Q9UKT9
  8. ↑ Phenocarta, Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants, https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_12236&ncbiId=22806, http://www.genome.gov/gwastudies/index.cfm?gene=IKZF3, 25. mai 2020
  9. ↑ 9,0 9,1 HomoloGene build68, 8269
  10. ↑ 10,0 10,1 Orthologous MAtrix, https://omabrowser.org/oma/vps/Q9UKT9/
  11. ↑ 11,00 11,01 11,02 11,03 11,04 11,05 11,06 11,07 11,08 11,09 Bgee, 7. juuni 2024, https://www.bgee.org/gene/ENSG00000161405
  12. ↑ Identifiers.org, http://www.ebi.ac.uk/miriam/main/collections/MIR:00000069
Pärit leheküljelt "https://et.wikipedia.org/wiki/Eri:AboutTopic/Q18036500"