IKZF2 (IKAROS family zinc finger 2)

2007-04-01   Rupa Sridharan  , Stephen Smale  

Room 6730 MacDonald Research Laboratories, Howard Hughes Medical Institute, 675 Charles Young Drive South, University of California, Los Angeles, CA 90095-1662, USA.

Identity

HGNC
LOCATION
2q34
LOCUSID
ALIAS
ANF1A2,HELIOS,ZNF1A2,ZNFN1A2
FUSION GENES

DNA/RNA

Description

143kb encoding 7 exons.

Transcription

12kb transcript, alternatively spliced to give two predominant isoforms.

Proteins

Note

526 amino acids. Mouse protein migrates at 70kD.
Atlas Image
Helios with the zinc finger domain shown as blocks and the exon junctions in black lines.

Description

Largest isoform contains four N-terminal zinc fingers used for DNA binding and two C terminal zinc fingers for homodimerization and heterodimerization with other Ikaros family members.

Expression

Largely restricted to the thymus. In mice, besides thymocytes and T cells, low levels are found in proB cells and bone marrow multipotent progenitors.

Localisation

Nuclear. Often localizes to the pericentric heterochromatin as punctate spots in cycling cells, with diffuse nuclear localization in non-cycling cells.

Function

Helios is thought to be important for T cell development and may function as a repressor of transcription. However, Helios mutant mice have not been reported. In mice, Helios can recruit the NuRD chromatin remodeling complex to the pericentric heterochromatin.

Homology

High level of identity to Ikaros over the zinc finger domains.

Implicated in

Entity name
Leukemia
Note
Shorter isoforms of Helios are expressed in certain human leukemias. They may function as dominant negative inhibitors of full-length proteins due to the lack of DNA binding domain. However, dominant negative functions have not been demonstrated experimentally.
Entity name
Lymphoma
Note
Overexpression of Helios in B cells of mice promotes lymphomagenesis. Overexpression of a DNA binding mutant in hematopoietic progenitors leads to aggressive and transplantable T cell lymphomas in 60% of the mice.

Article Bibliography

Pubmed IDLast YearTitleAuthors

Other Information

Locus ID:

NCBI: 22807
MIM: 606234
HGNC: 13177
Ensembl: ENSG00000030419

Variants:

dbSNP: 22807
ClinVar: 22807
TCGA: ENSG00000030419
COSMIC: IKZF2

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000030419ENST00000342002B4DWF2
ENSG00000030419ENST00000374319Q9UKS7
ENSG00000030419ENST00000374326Q9UKS7
ENSG00000030419ENST00000412444Q9UKS7
ENSG00000030419ENST00000431520Q9UKS7
ENSG00000030419ENST00000433134E7EUI1
ENSG00000030419ENST00000434687Q9UKS7
ENSG00000030419ENST00000439848Q9UKS7
ENSG00000030419ENST00000442445E7ES26
ENSG00000030419ENST00000451136A0A0A0MSL2
ENSG00000030419ENST00000452786E7EPU0
ENSG00000030419ENST00000453575Q9UKS7
ENSG00000030419ENST00000457361A0A0A0MT14

Expression (GTEx)

0
10
20
30
40
50
60
70
80

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
365100222023Aging-associated HELIOS deficiency in naive CD4(+) T cells alters chromatin remodeling and promotes effector cell responses.14
367386802023Decreased frequency of regulatory T cells and level of helios gene expression in secondary progressive multiple sclerosis patients: Evidence about the development of multiple sclerosis.1
373161892023Dominant negative variants in IKZF2 cause ICHAD syndrome, a new disorder characterised by immunodysregulation, craniofacial anomalies, hearing impairment, athelia and developmental delay.2
379969092023Temporal changes in regulatory T cell subsets defined by the transcription factor Helios in stroke and their potential role in stroke-associated infection: a prospective case-control study.0
365100222023Aging-associated HELIOS deficiency in naive CD4(+) T cells alters chromatin remodeling and promotes effector cell responses.14
367386802023Decreased frequency of regulatory T cells and level of helios gene expression in secondary progressive multiple sclerosis patients: Evidence about the development of multiple sclerosis.1
373161892023Dominant negative variants in IKZF2 cause ICHAD syndrome, a new disorder characterised by immunodysregulation, craniofacial anomalies, hearing impairment, athelia and developmental delay.2
379969092023Temporal changes in regulatory T cell subsets defined by the transcription factor Helios in stroke and their potential role in stroke-associated infection: a prospective case-control study.0
345618552022Helios is a marker, not a driver, of human Treg stability.25
349204542022Identification of germline monoallelic mutations in IKZF2 in patients with immune dysregulation.14
349817152022Expression of Programmed Cell Death 1 and Helios Genes Correlates With rs872071A>G and rs12203592C>T Single-Nucleotide Polymorphisms of InterferonRegulatory Factor 4 in Patients with T-Cell-Mediated Rejection of Renal Allograft.0
356516222022Co-Expression of TIGIT and Helios Marks Immunosenescent CD8(+) T Cells During Aging.5
345618552022Helios is a marker, not a driver, of human Treg stability.25
349204542022Identification of germline monoallelic mutations in IKZF2 in patients with immune dysregulation.14
349817152022Expression of Programmed Cell Death 1 and Helios Genes Correlates With rs872071A>G and rs12203592C>T Single-Nucleotide Polymorphisms of InterferonRegulatory Factor 4 in Patients with T-Cell-Mediated Rejection of Renal Allograft.0

Citation

Rupa Sridharan ; Stephen Smale

IKZF2 (IKAROS family zinc finger 2)

Atlas Genet Cytogenet Oncol Haematol. 2007-04-01

Online version: http://atlasgeneticsoncology.org/gene/42885/meetings/favicon/apple-touch-icon.png