Identity
HGNC
LOCATION
10q22.3
LOCUSID
ALIAS
ALS23,ANX11,CAP-50,CAP50
FUSION GENES
Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 311
MIM: 602572
HGNC: 535
Ensembl: ENSG00000122359
Variants:
dbSNP: 311
ClinVar: 311
TCGA: ENSG00000122359
COSMIC: ANXA11
RNA/Proteins
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 38896345 | 2024 | Annexin A11 aggregation in FTLD-TDP type C and related neurodegenerative disease proteinopathies. | 0 |
| 38896345 | 2024 | Annexin A11 aggregation in FTLD-TDP type C and related neurodegenerative disease proteinopathies. | 0 |
| 36008700 | 2023 | CircSOD2 Contributes to Tumor Progression, Immune Evasion and Anti-PD-1 Resistance in Hepatocellular Carcinoma by Targeting miR-497-5p/ANXA11 Axis. | 6 |
| 36651622 | 2023 | Common pathophysiology for ANXA11 disorders caused by aspartate 40 variants. | 0 |
| 36008700 | 2023 | CircSOD2 Contributes to Tumor Progression, Immune Evasion and Anti-PD-1 Resistance in Hepatocellular Carcinoma by Targeting miR-497-5p/ANXA11 Axis. | 6 |
| 36651622 | 2023 | Common pathophysiology for ANXA11 disorders caused by aspartate 40 variants. | 0 |
| 35463978 | 2022 | Subcellular Proteome Analysis Reveals Apoptotic Vulnerability of T-Cell Acute Lymphoblastic Leukemia. | 0 |
| 35563867 | 2022 | ANXA11 rs1049550 Associates with Löfgren's Syndrome and Chronic Sarcoidosis Patients. | 3 |
| 36134701 | 2022 | Adult-onset dominant muscular dystrophy in Greek families caused by Annexin A11. | 5 |
| 36280108 | 2022 | Genetic analysis of and clinical characteristics associated with ANXA11 variants in a Chinese cohort with amyotrophic lateral sclerosis. | 1 |
| 35463978 | 2022 | Subcellular Proteome Analysis Reveals Apoptotic Vulnerability of T-Cell Acute Lymphoblastic Leukemia. | 0 |
| 35563867 | 2022 | ANXA11 rs1049550 Associates with Löfgren's Syndrome and Chronic Sarcoidosis Patients. | 3 |
| 36134701 | 2022 | Adult-onset dominant muscular dystrophy in Greek families caused by Annexin A11. | 5 |
| 36280108 | 2022 | Genetic analysis of and clinical characteristics associated with ANXA11 variants in a Chinese cohort with amyotrophic lateral sclerosis. | 1 |
| 33218681 | 2021 | Genetic screening of ANXA11 revealed novel mutations linked to amyotrophic lateral sclerosis. | 15 |
Citation
Dessen P
ANXA11 (annexin A11)
Atlas Genet Cytogenet Oncol Haematol. 2009-11-01
Online version: http://atlasgeneticsoncology.org/gene/51241/anxa11
