Neidio i'r cynnwys

IKZF3

Ni chefnogir cynnwys y dudalen mewn ieithoedd eraill.
Creu erthygl

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protein-coding gene in the species Homo sapiens

Adnoddau allanol

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]
dynodwr Microsoft Academic
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]
dynodwr OMIM
606221[5]
dynodwr HGNC
13178[1]
HGNC gene symbol
IKZF3[1]
dynodwr Freebase
/m/03gyg9n

enghraifft o'r canlynol

genyn[3]

isddosbarth o'r canlynol

genyn codio-protein[6]

found in taxon

Homo sapiens[3]

amgodau

IKAROS family zinc finger 3[7]

genetic association

sirosis bustlaidd cynradd[8]

dull penderfynu: genome-wide association study, TAS

cromosom

cromosom dynol 17[3]

cynulliad genynnol: genome assembly GRCh38, Genome assembly GRCh37

strand orientation

edefyn ôl[3]

cynulliad genynnol: genome assembly GRCh38, Genome assembly GRCh37

genomic start

37921198[3]

cromosom: cromosom dynol 17

cynulliad genynnol: Genome assembly GRCh37

39757718[3]

cromosom: cromosom dynol 17

cynulliad genynnol: genome assembly GRCh38

genomic end

38020441[3]

cromosom: cromosom dynol 17

cynulliad genynnol: Genome assembly GRCh37

39864312[3]

cromosom: cromosom dynol 17

cynulliad genynnol: genome assembly GRCh38

cytogenetic location

17q12-q21.1[1]

HomoloGene ID

8269[1]

Gene Atlas image

ortholog

Ikzf3[9][10]

found in taxon: Llygoden y tŷ

Ikzf3[9][10]

found in taxon: brown rat

expressed in

granulocyte[11]

trefnolyn: 1

nod lymff[11]

trefnolyn: 2

epithelium of nasopharynx[11]

trefnolyn: 3

bone marrow cells[11]

trefnolyn: 4

Thymws[11]

trefnolyn: 5

Dueg[11]

trefnolyn: 6

gwaed[11]

trefnolyn: 7

Tonsil[11]

trefnolyn: 8

superficial temporal artery[11]

trefnolyn: 9

coluddyn crog[11]

trefnolyn: 10

cysyniad o'r un fath

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

Cyfeiriadau

  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 Ebrill 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 Mehefin 2023, inferred by common HGNC mappings on source and on Wikidata
  5. ↑ Online Mendelian Inheritance in Man, 19 Awst 2019
  6. ↑ Ensembl Release 87, ENSG00000161405
  7. ↑ UniProt, 6 Gorffennaf 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 Mehefin 2024, https://www.bgee.org/gene/ENSG00000161405
  12. ↑ Identifiers.org, http://www.ebi.ac.uk/miriam/main/collections/MIR:00000069
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