Fusion gene information | Fusion gene name: ANK2-ANK2 |
Fusion gene ID: hg287tg287 | | Hgene | Tgene | Gene symbol | ANK2 | ANK2 | Gene ID | 287 | 287 | Gene name | ankyrin 2 | ankyrin 2 |
Synonyms | ANK-2|CFAP87|FAP87|LQT4|brank-2 | ANK-2|CFAP87|FAP87|LQT4|brank-2 |
Cytomap | ('ANK2')('ANK2') 4q25-q26 | 4q25-q26 |
Type of gene | protein-coding | protein-coding |
Description | ankyrin-2ankyrin 2, neuronalankyrin Bankyrin, brainankyrin-2, nonerythrocyticnon-erythroid ankyrin | ankyrin-2ankyrin 2, neuronalankyrin Bankyrin, brainankyrin-2, nonerythrocyticnon-erythroid ankyrin |
Modification date | 20200313 | 20200313 |
UniProtAcc | . | . |
Ensembl transtripts involved in fusion gene | ENST00000264366, ENST00000357077, ENST00000394537, ENST00000504887, ENST00000506722, ENST00000509550, ENST00000510275, | ENST00000264366, ENST00000357077, ENST00000394537, ENST00000504887, ENST00000506722, ENST00000509550, ENST00000510275,
|
Fusion gene scores | * DoF score | 11 X 12 X 4=528 | 11 X 15 X 3=495 |
# samples | 15 | 15 |
** MAII score | log2(15/528*10)=-1.81557542886257 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(15/495*10)=-1.72246602447109 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 |
Context | PubMed: ANK2 [Title/Abstract] AND ANK2 [Title/Abstract] AND fusion [Title/Abstract] Defining the cellular phenotype of "ankyrin-B syndrome" variants: human ANK2 variants associated with clinical phenotypes display a spectrum of activities in cardiomyocytes (pmid: 17242276)
|
Most frequent breakpoint | ANK2(114274810)-ANK2(114275372), # samples:2 ANK2(114273906)-ANK2(114276867), # samples:2
|
Anticipated loss of major functional domain due to fusion event. | |
Hgene | Tgene |
. | . |
FUNCTION: Transcriptional activator which is required for calcium-dependent dendritic growth and branching in cortical neurons. Recruits CREB-binding protein (CREBBP) to nuclear bodies. Component of the CREST-BRG1 complex, a multiprotein complex that regulates promoter activation by orchestrating a calcium-dependent release of a repressor complex and a recruitment of an activator complex. In resting neurons, transcription of the c-FOS promoter is inhibited by BRG1-dependent recruitment of a phospho-RB1-HDAC1 repressor complex. Upon calcium influx, RB1 is dephosphorylated by calcineurin, which leads to release of the repressor complex. At the same time, there is increased recruitment of CREBBP to the promoter by a CREST-dependent mechanism, which leads to transcriptional activation. The CREST-BRG1 complex also binds to the NR2B promoter, and activity-dependent induction of NR2B expression involves a release of HDAC1 and recruitment of CREBBP (By similarity). {ECO:0000250}. | FUNCTION: Transcriptional activator which is required for calcium-dependent dendritic growth and branching in cortical neurons. Recruits CREB-binding protein (CREBBP) to nuclear bodies. Component of the CREST-BRG1 complex, a multiprotein complex that regulates promoter activation by orchestrating a calcium-dependent release of a repressor complex and a recruitment of an activator complex. In resting neurons, transcription of the c-FOS promoter is inhibited by BRG1-dependent recruitment of a phospho-RB1-HDAC1 repressor complex. Upon calcium influx, RB1 is dephosphorylated by calcineurin, which leads to release of the repressor complex. At the same time, there is increased recruitment of CREBBP to the promoter by a CREST-dependent mechanism, which leads to transcriptional activation. The CREST-BRG1 complex also binds to the NR2B promoter, and activity-dependent induction of NR2B expression involves a release of HDAC1 and recruitment of CREBBP (By similarity). {ECO:0000250}. |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | ANK2 | C1970119 | CARDIAC ARRHYTHMIA, ANKYRIN-B-RELATED | 5 | CTD_human;GENOMICS_ENGLAND;UNIPROT |
Hgene | ANK2 | C1142166 | Brugada Syndrome (disorder) | 4 | CLINGEN |
Hgene | ANK2 | C0035828 | Romano-Ward Syndrome | 3 | ORPHANET |
Hgene | ANK2 | C0038454 | Cerebrovascular accident | 1 | CTD_human |
Hgene | ANK2 | C0751956 | Acute Cerebrovascular Accidents | 1 | CTD_human |
Hgene | ANK2 | C1535926 | Neurodevelopmental Disorders | 1 | CTD_human |
Tgene | | C1970119 | CARDIAC ARRHYTHMIA, ANKYRIN-B-RELATED | 5 | CTD_human;GENOMICS_ENGLAND;UNIPROT |
Tgene | | C1142166 | Brugada Syndrome (disorder) | 4 | CLINGEN |
Tgene | | C0035828 | Romano-Ward Syndrome | 3 | ORPHANET |
Tgene | | C0038454 | Cerebrovascular accident | 1 | CTD_human |
Tgene | | C0751956 | Acute Cerebrovascular Accidents | 1 | CTD_human |
Tgene | | C1535926 | Neurodevelopmental Disorders | 1 | CTD_human |