ZFHX3 (AT-binding transcription factor 1)

2003-10-01   Nadine Van Roy  , Frank Speleman  

Center for Medical Genetics, Ghent University Hospital, 1K5, De Pintelaan 185, B-9000 Gent, Belgium

Identity

HGNC
LOCATION
16q22.2
IMAGE
Atlas Image
LEGEND
Probe(s) - Courtesy Mariano Rocchi, Resources for Molecular Cytogenetics
LOCUSID
ALIAS
ATBF1,ATBT,C16orf47,ZFH-3,ZNF927
FUSION GENES

DNA/RNA

Description

10 exons, DNA size: 261.32 kb.

Transcription

two isoforms ATBF1-A and ATBF1-B, due to alternative promotor usage combined with alternative splicing, mRNA-size: 11893 bp.

Proteins

Description

3703 amino acids; 404 kDa; four homeodomains and 23 zinc fingers including 1 pseudo zinc finger motif, one DEAD and one DEAH box, a RNA and an ATP binding site, two large RS domains and multiple phosphorylation sites.

Expression

Embryonic and neonatal brain.

Localisation

nuclear

Function

Transcription factor that binds to the AT-rich core sequence of the enhancer element of the AFP gene and downregulates AFP gene expression, possibly involved in neuronal differentiation (ATBF1-A).

Homology

mouse atbf1, drosophila zfh2 and C. Elegans ZC 123.3

Mutations

Somatic

Amplification, in one early neural crest derived cell line SJNB-12 under the form of extrachromosomally double minutes, non-syntenic co-amplification with MYC.
Absence of ATBF1 expression in alpha-fetoprotein expressing gastric cancer cell lines, lack of ATBF1 expression not due to mutation, deletion or translocation but to strong repression at the transcriptional level.

Implicated in

Disease
Early neural crest derived cell line (SJNB-12).
Prognosis
unknown
Cytogenetics
Several structural and numerical chromosomal aberrations and presence of extrachromosomally double minutes and homogenously staining regions, presence of a reciprocal unbalanced t(8;16)(q24.3;q22.3).
Oncogenesis
Amplification in one neural crest derived cell line (SJNB-12), non-syntenic co-amplification with MYC.
Disease
Alpha-fetoprotein producing gastric cancer cell lines (GCIY and Ist-I).
Prognosis
poor (very malignant and highly metastatic cancer)
Oncogenesis
Alpha-fetoprotein producing cancer cell lines show absence of ATBF1 expression, lack of ATBF1 expression not due to deletion mutation or translocation but to strong repression at the transcriptional level.

Bibliography

Pubmed IDLast YearTitleAuthors

Other Information

Locus ID:

NCBI: 463
MIM: 104155
HGNC: 777
Ensembl: ENSG00000140836

Variants:

dbSNP: 463
ClinVar: 463
TCGA: ENSG00000140836
COSMIC: ZFHX3

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000140836ENST00000268489Q15911
ENSG00000140836ENST00000397992Q15911
ENSG00000140836ENST00000641206Q15911

Expression (GTEx)

0
5
10
15
20
25
30
35

Pathways

PathwaySourceExternal ID
Signaling pathways regulating pluripotency of stem cellsKEGGhsa04550
Signaling pathways regulating pluripotency of stem cellsKEGGko04550

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
380358812024Exonic trinucleotide repeat expansions in ZFHX3 cause spinocerebellar ataxia type 4: A poly-glycine disease.2
381971342024Adaptive Long-Read Sequencing Reveals GGC Repeat Expansion in ZFHX3 Associated with Spinocerebellar Ataxia Type 4.0
382273692024Myeloid Zfhx3 deficiency protects against hypercapnia-induced suppression of host defense against influenza A virus.0
384128612024Haploinsufficiency of ZFHX3, encoding a key player in neuronal development, causes syndromic intellectual disability.0
385087052024ZFHX3 variants cause childhood partial epilepsy and infantile spasms with favourable outcomes.0
380358812024Exonic trinucleotide repeat expansions in ZFHX3 cause spinocerebellar ataxia type 4: A poly-glycine disease.2
381971342024Adaptive Long-Read Sequencing Reveals GGC Repeat Expansion in ZFHX3 Associated with Spinocerebellar Ataxia Type 4.0
382273692024Myeloid Zfhx3 deficiency protects against hypercapnia-induced suppression of host defense against influenza A virus.0
384128612024Haploinsufficiency of ZFHX3, encoding a key player in neuronal development, causes syndromic intellectual disability.0
385087052024ZFHX3 variants cause childhood partial epilepsy and infantile spasms with favourable outcomes.0
368001422023Influence of ZFHX3 Polymorphisms on the Risk of Ischemic Stroke in Chinese Han Population.1
374494012023Loss of the Atrial Fibrillation-Related Gene, Zfhx3, Results in Atrial Dilation and Arrhythmias.4
368001422023Influence of ZFHX3 Polymorphisms on the Risk of Ischemic Stroke in Chinese Han Population.1
374494012023Loss of the Atrial Fibrillation-Related Gene, Zfhx3, Results in Atrial Dilation and Arrhythmias.4
349530442022AR imposes different effects on ZFHX3 transcription depending on androgen status in prostate cancer cells.3

Citation

Nadine Van Roy ; Frank Speleman

ZFHX3 (AT-binding transcription factor 1)

Atlas Genet Cytogenet Oncol Haematol. 2003-10-01

Online version: http://atlasgeneticsoncology.org/gene/357/favicon/favicon/favicon-32x32.png