ARID2 (AT-rich interaction domain 2)

2011-10-01  

Identity

HGNC
LOCATION
12q12
LOCUSID
ALIAS
BAF200,CSS6,p200
FUSION GENES

Other Information

Locus ID:

NCBI: 196528
MIM: 609539
HGNC: 18037
Ensembl: ENSG00000189079

Variants:

dbSNP: 196528
ClinVar: 196528
TCGA: ENSG00000189079
COSMIC: ARID2

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000189079ENST00000334344Q68CP9
ENSG00000189079ENST00000422737F8WCU9
ENSG00000189079ENST00000444670F8W108
ENSG00000189079ENST00000457135F8VWP4
ENSG00000189079ENST00000477947A0A087WY37

Expression (GTEx)

0
5
10
15
20
25
30

Pathways

PathwaySourceExternal ID
Chromatin organizationREACTOMER-HSA-4839726
Chromatin modifying enzymesREACTOMER-HSA-3247509
RMTs methylate histone argininesREACTOMER-HSA-3214858

References

Pubmed IDYearTitleCitations
382434072024ARID2, a milder cause of Coffin-Siris Syndrome? Broadening the phenotype with 17 additional individuals.0
383415152024ARID2 mutations may relay a distinct subset of cutaneous melanoma patients with different outcomes.0
382434072024ARID2, a milder cause of Coffin-Siris Syndrome? Broadening the phenotype with 17 additional individuals.0
383415152024ARID2 mutations may relay a distinct subset of cutaneous melanoma patients with different outcomes.0
365300292023miR-29a-5p regulates the malignant biological process of liver cancer cells through ARID2 regulation of EMT.1
367568592023ARID2, a rare cause of Coffin-Siris syndrome: A novel microdeletion at 12q12q13.11 causing severe short stature and literature review.1
381821562023Coffin-Siris Syndrome: Case Series of Three Patients and a Novel ARID2 Variant.0
365300292023miR-29a-5p regulates the malignant biological process of liver cancer cells through ARID2 regulation of EMT.1
367568592023ARID2, a rare cause of Coffin-Siris syndrome: A novel microdeletion at 12q12q13.11 causing severe short stature and literature review.1
381821562023Coffin-Siris Syndrome: Case Series of Three Patients and a Novel ARID2 Variant.0
350176652022BRD4 inhibition induces synthetic lethality in ARID2-deficient hepatocellular carcinoma by increasing DNA damage.6
353857312022Altered BAF occupancy and transcription factor dynamics in PBAF-deficient melanoma.13
358692772022ARID2 suppression promotes tumor progression and upregulates cytokeratin 8, 18 and β-4 integrin expression in TP53-mutated tobacco-related oral cancer and has prognostic implications.4
365679032022USP2 Inhibits Lung Cancer Pathogenesis by Reducing ARID2 Protein Degradation via Ubiquitination.3
350176652022BRD4 inhibition induces synthetic lethality in ARID2-deficient hepatocellular carcinoma by increasing DNA damage.6

Citation

Dessen P

ARID2 (AT-rich interaction domain 2)

Atlas Genet Cytogenet Oncol Haematol. 2011-10-01

Online version: http://atlasgeneticsoncology.org/gene/52470/arid2-(at-rich-interaction-domain-2)