ವಿಷಯಕ್ಕೆ ಹೋಗು

IKZF3

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protein-coding gene in the species Homo sapiens

External resources

RefSeq RNA ID
NM_183232[೧]
NM_001257408[೧]
NM_001257409[೧]
NM_001257410[೧]
NM_001257411[೧]
NM_001257412[೧]
NM_001257413[೧]
NM_001257414[೧]
NM_001284514[೧]
NM_001284515[೧]
NM_001284516[೧]
NM_012481[೧]
NM_183228[೧]
NM_183229[೧]
NM_183230[೧]
NM_183231[೧]
XM_047435625[೨]
Microsoft Academic ID
2779480474
Ensembl transcript ID
ENST00000623724[೩]
ENST00000293068[೩]
ENST00000346243[೩]
ENST00000346872[೩]
ENST00000348427[೩]
ENST00000350532[೩]
ENST00000351680[೩]
ENST00000377944[೩]
ENST00000377945[೩]
ENST00000377952[೩]
ENST00000377958[೩]
ENST00000394189[೩]
ENST00000439016[೩]
ENST00000439167[೩]
ENST00000467757[೩]
ENST00000535189[೩]
ENST00000583368[೩]
Entrez Gene ID
22806[೧]
UMLS CUI
C1825590[೪]
Ensembl gene ID
ENSG00000161405[೩]
OMIM ID
606221[೫]
HGNC ID
13178[೧]
HGNC gene symbol
IKZF3[೧]
Freebase ಐಡಿ
/m/03gyg9n

ಉದಾಹರಣೆಗೆ

ವಂಶವಾಹಿ[೩]

ಉಪವರ್ಗ

protein-coding gene[೬]

found in taxon

Homo sapiens[೩]

encodes

IKAROS family zinc finger 3[೭]

genetic association

primary biliary cholangitis[೮]

determination method: genome-wide association study, TAS

chromosome

human chromosome 17[೩]

genomic assembly: genome assembly GRCh38, Genome assembly GRCh37

strand orientation

reverse strand[೩]

genomic assembly: genome assembly GRCh38, Genome assembly GRCh37

genomic start

37921198[೩]

chromosome: human chromosome 17

genomic assembly: Genome assembly GRCh37

39757718[೩]

chromosome: human chromosome 17

genomic assembly: genome assembly GRCh38

genomic end

38020441[೩]

chromosome: human chromosome 17

genomic assembly: Genome assembly GRCh37

39864312[೩]

chromosome: human chromosome 17

genomic assembly: genome assembly GRCh38

cytogenetic location

17q12-q21.1[೧]

HomoloGene ID

8269[೧]

Gene Atlas image

ortholog

Ikzf3[೯][೧೦]

found in taxon: house mouse

Ikzf3[೯][೧೦]

found in taxon: brown rat

expressed in

granulocyte[೧೧]

series ordinal: 1

ದುಗ್ಧರಸ ಗ್ರಂಥಿ[೧೧]

series ordinal: 2

epithelium of nasopharynx[೧೧]

series ordinal: 3

bone marrow cells[೧೧]

series ordinal: 4

thymus[೧೧]

series ordinal: 5

ಗುಲ್ಮ[೧೧]

series ordinal: 6

ರಕ್ತ[೧೧]

series ordinal: 7

tonsil[೧೧]

series ordinal: 8

superficial temporal artery[೧೧]

series ordinal: 9

appendix[೧೧]

series ordinal: 10

exact match

http://identifiers.org/ncbigene/22806[೧೨]

Reference

  1. ↑ ೧.೦೦ ೧.೦೧ ೧.೦೨ ೧.೦೩ ೧.೦೪ ೧.೦೫ ೧.೦೬ ೧.೦೭ ೧.೦೮ ೧.೦೯ ೧.೧೦ ೧.೧೧ ೧.೧೨ ೧.೧೩ ೧.೧೪ ೧.೧೫ ೧.೧೬ ೧.೧೭ ೧.೧೮ ೧.೧೯ ೧.೨೦ NCBI Gene, ೧೫ ಮೇ 2022, 22806
  2. ↑ NCBI Gene, ೧೦ ಏಪ್ರಿಲ್ 2022, 22806
  3. ↑ ೩.೦೦ ೩.೦೧ ೩.೦೨ ೩.೦೩ ೩.೦೪ ೩.೦೫ ೩.೦೬ ೩.೦೭ ೩.೦೮ ೩.೦೯ ೩.೧೦ ೩.೧೧ ೩.೧೨ ೩.೧೩ ೩.೧೪ ೩.೧೫ ೩.೧೬ ೩.೧೭ ೩.೧೮ ೩.೧೯ ೩.೨೦ ೩.೨೧ ೩.೨೨ ೩.೨೩ ೩.೨೪ ೩.೨೫ ensembl Release 106, ENSG00000161405
  4. ↑ UMLS 2023, ೧೫ ಜೂನ್ 2023, inferred by common HGNC mappings on source and on Wikidata
  5. ↑ Online Mendelian Inheritance in Man, ೧೯ ಆಗಸ್ಟ್ 2019
  6. ↑ Ensembl Release 87, ENSG00000161405
  7. ↑ UniProt, ೬ ಜುಲೈ 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, ೨೫ ಮೇ 2020
  9. ↑ ೯.೦ ೯.೧ HomoloGene build68, 8269
  10. ↑ ೧೦.೦ ೧೦.೧ Orthologous MAtrix, https://omabrowser.org/oma/vps/Q9UKT9/
  11. ↑ ೧೧.೦೦ ೧೧.೦೧ ೧೧.೦೨ ೧೧.೦೩ ೧೧.೦೪ ೧೧.೦೫ ೧೧.೦೬ ೧೧.೦೭ ೧೧.೦೮ ೧೧.೦೯ Bgee, ೭ ಜೂನ್ 2024, https://www.bgee.org/gene/ENSG00000161405
  12. ↑ Identifiers.org, http://www.ebi.ac.uk/miriam/main/collections/MIR:00000069
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