Basic information
Biomarker: SMA
Histology type: endometrial stromal tumor
Cohort characteristics
Country: China
Region: Beijing
Followed up time :
Subgroup 1 name : positive
Subgroup 1 number: 5
Subgroup 2 name: negative
Subgroup 2 number: 13
Total number | Group I | Group I number | Group II | Group II number | Group III | Group III number | Group IV | Group IV number |
---|---|---|---|---|---|---|---|---|
19 | ESS | 15 | metastases | 4 |
Sample information
Conclusion: The histologic features of the metastases may not be similar to those of the primary. SMA is diagnostically useful markers for ESS.
Sample type : tissue
Sample method: immunohistochemistry
Expression pattern : positive expression
Disease information
Statictics: Mean ;Range
Cohort age: 45;22-75
Related information
Funtion Uniprot: Actins are highly conserved proteins that are involved in various types of cell motility and are ubiquitously expressed in all eukaryotic cells.
UniProt ID: P63267
UniProt Link: https://www.uniprot.org/uniprotkb/P63267/entry
Molecular function from UniProt:
Tissue specificity from UniProt: In the intestine, abundantly expressed in smooth muscle cells of muscularis mucosa and muscularis propria. Also detected in intestinal vascular smooth muscle cells.
Subcellular UniProt: #Cytoplasm #Cytoskeleton
Alternative name from UniProt:
Cleaved: Cleaved into 1 chains Actin, gamma-enteric smooth muscle, intermediate form
Miscellaneous: In vertebrates 3 main groups of actin isoforms, alpha, beta and gamma have been identified. The alpha actins are found in muscle tissues and are a major constituent of the contractile apparatus. The beta and gamma actins coexist in most cell types as components of the cytoskeleton and as mediators of internal cell motility.
Recommended name: Actin, gamma-enteric smooth muscle
Gene name from HGNC: ACTG2 (ACTA3, ACTL3, ACTSG)
HPA class: Disease related genes Human disease related genes
AlphaFold DB: P63267
AlphaFold Link: https://alphafold.ebi.ac.uk/entry/P63267
HPA link: https://www.proteinatlas.org/ENSG00000163017-ACTG2
Tissue specificity RNA from HPA: Tissue enhanced (intestine, seminal vesicle, smooth muscle)
Tissue expression from HPA: Cytoplasmic expression of myoepithelial cells.
Single cell type specificity Group enriched (Breast myoepithelial cells, Smooth muscle cells)
Immune cell specificity: Immune cell enriched (T-reg)
Cancer prognostic summary HPA Prognostic marker in renal cancer (unfavorable)
Pathology link: https://www.proteinatlas.org/ENSG00000163017-ACTG2/pathology
Pathology endo: https://www.proteinatlas.org/ENSG00000163017-ACTG2/pathology/endometrial+cancer
Phenotype ID: 155310;619431;
Disease: Visceral myopathy 1 (VSCM1);Megacystis-microcolon-intestinal hypoperistalsis syndrome 5 (MMIHS5);
Note1: The disease is caused by variants affecting the gene represented in this entry;The disease is caused by variants affecting the gene represented in this entry;
Note2: A number sign (#) is used with this entry because of evidence that visceral myopathy-1 (VSCM1) is caused by heterozygous mutation in the ACTG2 gene (102545) on chromosome 2p13.;A number sign (#) is used with this entry because of evidence that megacystis-microcolon-intestinal hypoperistalsis syndrome-5 (MMIHS5) is caused by heterozygous mutation in the ACTG2 gene (102545) on chromosome 2p13. Visceral myopathy-1 (VSCM1; 155310), which overlaps phenotypically with MMIHS5, is also caused by heterozygous mutation in the ACTG2 gene.;
OMIM: 102545;155310;619431;
OMIM link1: https://www.omim.org/entry/155310;https://www.omim.org/entry/619431;
OMIM link2: https://www.omim.org/entry/102545;https://www.omim.org/entry/155310;https://www.omim.org/entry/619431;
Phenotype: Visceral myopathy 1;Megacystis-microcolon-intestinal hypoperistalsis syndrome 5 ;
HGNC ID: HGNC:145
HGNC link: https://www.genenames.org/data/gene-symbol-report/#!/hgnc_id/HGNC:145