Basic information

Biomarker: ARID1A

Histology type: endometrioid endometrial carcinoma

Stage: high grade

Cohort characteristics

Country: Turkey

Region: Istanbul

Followed up time :

Subgroup 1 name : ARID1A loss

Subgroup 1 number: 13

Subgroup 2 name: ARID1A retained

Subgroup 2 number: 46

Total number Group I Group I number Group II Group II number Group III Group III number Group IV Group IV number
59 EC 59

Sample information

Conclusion: We observed that ARID1A loss was more common in high-grade endometrioid endometrial carcinoma s .

Sample type : tissue

Sample method: immunohistochemistry

Expression pattern : loss

Expression elevation: ARID1A, loss of expression in TCs was defined as complete absence of nuclear staining with positive nuclear staining of external and internal nonneoplastic controls (lymphoid, endothelial, and stromal cells)

Disease information

Statictics: cutoff<60;cutoff>60

Subgroup 1 age: 6;7

Related information

Funtion Uniprot: Involved in transcriptional activation and repression of select genes by chromatin remodeling (alteration of DNA-nucleosome topology). Component of SWI/SNF chromatin remodeling complexes that carry out key enzymatic activities, changing chromatin structure by altering DNA-histone contacts within a nucleosome in an ATP-dependent manner. Binds DNA non-specifically. Belongs to the neural progenitors-specific chromatin remodeling complex (npBAF complex) and the neuron-specific chromatin remodeling complex (nBAF complex). During neural development a switch from a stem/progenitor to a postmitotic chromatin remodeling mechanism occurs as neurons exit the cell cycle and become committed to their adult state. The transition from proliferating neural stem/progenitor cells to postmitotic neurons requires a switch in subunit composition of the npBAF and nBAF complexes. As neural progenitors exit mitosis and differentiate into neurons, npBAF complexes which contain ACTL6A/BAF53A and PHF10/BAF45A, are exchanged for homologous alternative ACTL6B/BAF53B and DPF1/BAF45B or DPF3/BAF45C subunits in neuron-specific complexes (nBAF). The npBAF complex is essential for the self-renewal/proliferative capacity of the multipotent neural stem cells. The nBAF complex along with CREST plays a role regulating the activity of genes essential for dendrite growth (By similarity).

UniProt ID: O14497

UniProt Link: https://www.uniprot.org/uniprotkb/O14497/entry

Biological function from UniProt: #Neurogenesis #Transcription #Transcription regulation

Molecular function from UniProt:

Tissue specificity from UniProt: Highly expressed in spleen, thymus, prostate, testis, ovary, small intestine, colon, and PBL, and at a much lower level in heart, brain, placenta, lung, liver, skeletal muscle, kidney, and pancreas.

Subcellular UniProt: #Nucleus

Alternative name from UniProt:

Recommended name: AT-rich interactive domain-containing protein 1A

Gene name from HGNC: ARID1A (B120, BAF250, BAF250a, C10rf4, C1orf4, P270, SMARCF1)

HPA class: Cancer-related genes Disease related genes Human disease related genes Transcription factors

AlphaFold DB: O14497

AlphaFold Link: https://alphafold.ebi.ac.uk/entry/O14497

HPA link: https://www.proteinatlas.org/ENSG00000117713-ARID1A

Tissue specificity RNA from HPA: Low tissue specificity

Tissue expression from HPA: Ubiquitous nuclear expression.

Single cell type specificity Low cell type specificity

Immune cell specificity: Low immune cell specificity

Subcellular summary HPA Located in Nucleoplasm (CCD Transcript)

Cancer prognostic summary HPA Prognostic marker in liver cancer (unfavorable)

Pathology link: https://www.proteinatlas.org/ENSG00000117713-ARID1A/pathology

Pathology endo: https://www.proteinatlas.org/ENSG00000117713-ARID1A/pathology/endometrial+cancer

Phenotype ID: 614607

Disease: Coffin-Siris syndrome 2 (CSS2)

Note1: The disease is caused by variants affecting the gene represented in this entry

OMIM: 603024

OMIM link1: https://www.omim.org/entry/614607

OMIM link2: https://www.omim.org/entry/603024

HGNC ID: HGNC:11110

HGNC link: https://www.genenames.org/data/gene-symbol-report/#!/hgnc_id/HGNC:11110

Visulization