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: 7840
MIM: 606844
HGNC: 428
Ensembl: ENSG00000116127
Variants:
dbSNP: 7840
ClinVar: 7840
TCGA: ENSG00000116127
COSMIC: ALMS1
RNA/Proteins
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 37937857 | 2024 | Unraveling Alström syndrome: Homozygous mutation c.2729C>G in ALMS1 gene across an extended family. | 1 |
| 38122899 | 2024 | Interactome Analysis Reveals a Link of the Novel ALMS1-CEP70 Complex to Centrosomal Clusters. | 0 |
| 38428329 | 2024 | New variants of ALMS1 gene and familial Alström syndrome case series. | 0 |
| 38497483 | 2024 | CircALMS1 Alleviates Pulmonary Microvascular Endothelial Cell Dysfunction in Pulmonary Hypertension. | 0 |
| 38546151 | 2024 | Overburden of rare ALMS1 deleterious variants in Chinese early-onset type 2 diabetes with severe insulin resistance. | 1 |
| 37937857 | 2024 | Unraveling Alström syndrome: Homozygous mutation c.2729C>G in ALMS1 gene across an extended family. | 1 |
| 38122899 | 2024 | Interactome Analysis Reveals a Link of the Novel ALMS1-CEP70 Complex to Centrosomal Clusters. | 0 |
| 38428329 | 2024 | New variants of ALMS1 gene and familial Alström syndrome case series. | 0 |
| 38497483 | 2024 | CircALMS1 Alleviates Pulmonary Microvascular Endothelial Cell Dysfunction in Pulmonary Hypertension. | 0 |
| 38546151 | 2024 | Overburden of rare ALMS1 deleterious variants in Chinese early-onset type 2 diabetes with severe insulin resistance. | 1 |
| 38062477 | 2023 | Loss of the centrosomal protein ALMS1 alters lipid metabolism and the regulation of extracellular matrix-related processes. | 0 |
| 38062477 | 2023 | Loss of the centrosomal protein ALMS1 alters lipid metabolism and the regulation of extracellular matrix-related processes. | 0 |
| 35292292 | 2022 | Whole-Genome Sequencing Identifies Novel Heterozygous Mutation in ALMS1 in Three Men With Both Peyronie's and Dupuytren's Disease. | 2 |
| 35786123 | 2022 | Identification of ALMS1 pathogenic variants in Chinese patients with Alström syndrome. | 0 |
| 36162988 | 2022 | New pathogenic variants of ALMS1 gene in two Chinese families with Alström Syndrome. | 0 |
Citation
Dessen P
ALMS1 (ALMS1 centrosome and basal body associated protein)
Atlas Genet Cytogenet Oncol Haematol. 2015-09-01
Online version: http://atlasgeneticsoncology.org/gene/55396/alms1-(alms1-centrosome-and-basal-body-associated-protein)
