ଉଇକିପିଡ଼ିଆ

IKZF3

ପ୍ରସଙ୍ଗଟିଏ ଗଢ଼ନ୍ତୁ

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protein-coding gene in the species Homo sapiens

External resources

RefSeq RNA ID
NM_183232[୧]
NM_001257408[୧]
NM_001257409[୧]
NM_001257410[୧]
NM_001257411[୧]
NM_001257412[୧]
NM_001257413[୧]
NM_001257414[୧]
NM_001284514[୧]
NM_001284515[୧]
NM_001284516[୧]
NM_012481[୧]
NM_183228[୧]
NM_183229[୧]
NM_183230[୧]
NM_183231[୧]
XM_047435625[୨]
Microsoft Academic ID
2779480474
Ensembl transcript ID
ENST00000623724[୩]
ENST00000293068[୩]
ENST00000346243[୩]
ENST00000346872[୩]
ENST00000348427[୩]
ENST00000350532[୩]
ENST00000351680[୩]
ENST00000377944[୩]
ENST00000377945[୩]
ENST00000377952[୩]
ENST00000377958[୩]
ENST00000394189[୩]
ENST00000439016[୩]
ENST00000439167[୩]
ENST00000467757[୩]
ENST00000535189[୩]
ENST00000583368[୩]
Entrez Gene ID
22806[୧]
UMLS CUI
C1825590[୪]
Ensembl gene ID
ENSG00000161405[୩]
OMIM ID
606221[୫]
HGNC ID
13178[୧]
HGNC gene symbol
IKZF3[୧]
ଫ୍ରୀବେସ ସୂଚକ
/m/03gyg9n

ଦୃଷ୍ଟାନ୍ତ

ଜୀନ[୩]

ଏହାର ମୁଖ୍ୟଶ୍ରେଣୀ

protein-coding gene[୬]

found in taxon

Homo sapiens[୩]

encodes

IKAROS family zinc finger 3[୭]

genetic association

ପ୍ରାଥମିକ ବିଲିଆରି କୋଲାଞ୍ଜାଇଟିସ୍ ‎[୮]

determination method or standard: genome-wide association study, TAS

chromosome

human chromosome 17[୩]

genomic assembly: genome assembly GRCh38, Genome assembly GRCh37

strand orientation

reverse strand[୩]

genomic assembly: genome assembly GRCh38, Genome assembly GRCh37

genomic start

37921198[୩]

genomic assembly: Genome assembly GRCh37

chromosome: human chromosome 17

39757718[୩]

genomic assembly: genome assembly GRCh38

chromosome: human chromosome 17

genomic end

38020441[୩]

genomic assembly: Genome assembly GRCh37

chromosome: human chromosome 17

39864312[୩]

genomic assembly: genome assembly GRCh38

chromosome: human chromosome 17

cytogenetic location

17q12-q21.1[୧]

HomoloGene ID

8269[୧]

Gene Atlas image

ortholog

Ikzf3[୯][୧୦]

found in taxon: house mouse

Ikzf3[୯][୧୦]

found in taxon: brown rat

expressed in

granulocyte[୧୧]

series ordinal: 1

lymph node[୧୧]

series ordinal: 2

epithelium of nasopharynx[୧୧]

series ordinal: 3

bone marrow cells[୧୧]

series ordinal: 4

thymus[୧୧]

series ordinal: 5

ପ୍ଲୀହା[୧୧]

series ordinal: 6

ରକ୍ତ[୧୧]

series ordinal: 7

tonsil[୧୧]

series ordinal: 8

superficial temporal artery[୧୧]

series ordinal: 9

appendix[୧୧]

series ordinal: 10

exact match

http://identifiers.org/ncbigene/22806[୧୨]

ଆଧାର

  1. ↑ ୧.୦୦ ୧.୦୧ ୧.୦୨ ୧.୦୩ ୧.୦୪ ୧.୦୫ ୧.୦୬ ୧.୦୭ ୧.୦୮ ୧.୦୯ ୧.୧୦ ୧.୧୧ ୧.୧୨ ୧.୧୩ ୧.୧୪ ୧.୧୫ ୧.୧୬ ୧.୧୭ ୧.୧୮ ୧.୧୯ ୧.୨୦ NCBI Gene, ୧୫ ମଇ 2022, 22806
  2. ↑ NCBI Gene, ୧୦ ଅପ୍ରେଲ 2022, 22806
  3. ↑ ୩.୦୦ ୩.୦୧ ୩.୦୨ ୩.୦୩ ୩.୦୪ ୩.୦୫ ୩.୦୬ ୩.୦୭ ୩.୦୮ ୩.୦୯ ୩.୧୦ ୩.୧୧ ୩.୧୨ ୩.୧୩ ୩.୧୪ ୩.୧୫ ୩.୧୬ ୩.୧୭ ୩.୧୮ ୩.୧୯ ୩.୨୦ ୩.୨୧ ୩.୨୨ ୩.୨୩ ୩.୨୪ ୩.୨୫ ensembl Release 106, ENSG00000161405
  4. ↑ UMLS 2023, ୧୫ ଜୁନ 2023, inferred by common HGNC mappings on source and on Wikidata
  5. ↑ Online Mendelian Inheritance in Man, ୧୯ ଅଗଷ୍ଟ 2019
  6. ↑ Ensembl Release 87, ENSG00000161405
  7. ↑ UniProt, ୬ ଜୁଲାଇ 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, ୨୫ ମଇ 2020
  9. ↑ ୯.୦ ୯.୧ HomoloGene build68, 8269
  10. ↑ ୧୦.୦ ୧୦.୧ Orthologous MAtrix, https://omabrowser.org/oma/vps/Q9UKT9/
  11. ↑ ୧୧.୦୦ ୧୧.୦୧ ୧୧.୦୨ ୧୧.୦୩ ୧୧.୦୪ ୧୧.୦୫ ୧୧.୦୬ ୧୧.୦୭ ୧୧.୦୮ ୧୧.୦୯ Bgee, ୭ ଜୁନ 2024, https://www.bgee.org/gene/ENSG00000161405
  12. ↑ Identifiers.org, http://www.ebi.ac.uk/miriam/main/collections/MIR:00000069
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