IKZF3

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gene umano

Risorse esterne

identificativo RNA	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]
identificativo Microsoft Academic	2779480474
identificativo trascrizione Ensembl	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]
identificativo gene Entrez	22806^[1]
UMLS CUI	C1825590^[4]
identificativo gene Ensembl	ENSG00000161405^[3]
identificativo OMIM	606221^[5]
identificativo HGNC	13178^[1]
simbolo gene	IKZF3^[1]
identificativo Freebase	/m/03gyg9n

no tipo 'e

gene^[3]

sottoclasse di

gene codificante una proteina^[6]

trovato nella tassonomia de

Homo sapiens^[3]

codifica

IKAROS family zinc finger 3^[7]

associazione genetica

cirrosi biliare primitiva^[8]

metodo di determinazione: studio di associazione genome-wide, TAS

cromosoma

cromosoma 17^[3]

assemblaggio genomico: genome assembly GRCh38, Genome assembly GRCh37

orientamento del filamento

reverse strand^[3]

assemblaggio genomico: genome assembly GRCh38, Genome assembly GRCh37

inizio della sequenza genomica

37921198^[3]

assemblaggio genomico: Genome assembly GRCh37

cromosoma: cromosoma 17

39757718^[3]

assemblaggio genomico: genome assembly GRCh38

cromosoma: cromosoma 17

fine della sequenza genomica

38020441^[3]

assemblaggio genomico: Genome assembly GRCh37

cromosoma: cromosoma 17

39864312^[3]

assemblaggio genomico: genome assembly GRCh38

cromosoma: cromosoma 17

posizione citogenetica

17q12-q21.1^[1]

identificativo Homologene

8269^[1]

immagine Gene Atlas

ortologo

Ikzf3^[9]^[10]

trovato nella tassonomia de: Surice

Ikzf3^[9]^[10]

trovato nella tassonomia de: ratto grigio

expressed in

granulocita^[11]

numero d'ordine: 1

linfonodo^[11]

numero d'ordine: 2

epithelium of nasopharynx^[11]

numero d'ordine: 3

bone marrow cells^[11]

numero d'ordine: 4

timo^[11]

numero d'ordine: 5

milza^[11]

numero d'ordine: 6

sangue^[11]

numero d'ordine: 7

tonsilla^[11]

numero d'ordine: 8

arteria temporale superficiale^[11]

numero d'ordine: 9

appendice vermiforme^[11]

numero d'ordine: 10

corrisponde esattamente

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

Riferimento

↑ ^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 Maj 2022, 22806
↑ NCBI Gene, 10 Abb 2022, 22806
↑ ^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
↑ UMLS 2023, 15 Giù 2023, inferred by common HGNC mappings on source and on Wikidata
↑ Mendelian Inheritance in Man, 19 Aùs 2019
↑ Ensembl Release 87, ENSG00000161405
↑ UniProt, 6 lug 2017, Q9UKT9
↑ 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 Maj 2020
↑ ^9,0 ^9,1 HomoloGene build68, 8269
↑ ^10,0 ^10,1 Orthologous MAtrix, https://omabrowser.org/oma/vps/Q9UKT9/
↑ ^11,00 ^11,01 ^11,02 ^11,03 ^11,04 ^11,05 ^11,06 ^11,07 ^11,08 ^11,09 Bgee, 7 Giù 2024, https://www.bgee.org/gene/ENSG00000161405
↑ registro identifiers.org, http://www.ebi.ac.uk/miriam/main/collections/MIR:00000069

[rd8f3aa5b-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 Maj 2022, 22806

[rf8674644-2] NCBI Gene, 10 Abb 2022, 22806

[rd583f86e-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

[r0d78b83c-4] UMLS 2023, 15 Giù 2023, inferred by common HGNC mappings on source and on Wikidata

[rdbdfa9c6-5] Mendelian Inheritance in Man, 19 Aùs 2019

[r3e244445-6] Ensembl Release 87, ENSG00000161405

[rff0e2b00-7] UniProt, 6 lug 2017, Q9UKT9

[r59221d05-8] 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 Maj 2020

[r026c7571-9] 9,0 ^9,1 HomoloGene build68, 8269

[r2366b448-10] 10,0 ^10,1 Orthologous MAtrix, https://omabrowser.org/oma/vps/Q9UKT9/

[rde59def9-11] 11,00 ^11,01 ^11,02 ^11,03 ^11,04 ^11,05 ^11,06 ^11,07 ^11,08 ^11,09 Bgee, 7 Giù 2024, https://www.bgee.org/gene/ENSG00000161405

[rf84d0be1-12] registro identifiers.org, http://www.ebi.ac.uk/miriam/main/collections/MIR:00000069

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