Gene Gene information from NCBI Gene database.
Entrez ID 84319
Gene name Cms1 ribosomal small subunit homolog
Gene symbol CMSS1
Synonyms (NCBI Gene)
C3orf26
Chromosome 3
Chromosome location 3q12.1
miRNA miRNA information provided by mirtarbase database.
57
miRTarBase ID miRNA Experiments Reference
MIRT020861 hsa-miR-155-5p Proteomics 18668040
MIRT526945 hsa-miR-4323 PAR-CLIP 20371350
MIRT526946 hsa-miR-4687-5p PAR-CLIP 20371350
MIRT526944 hsa-miR-4758-3p PAR-CLIP 20371350
MIRT526943 hsa-miR-4290 PAR-CLIP 20371350
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
2
GO ID Ontology Definition Evidence Reference
GO:0003723 Function RNA binding HDA 22658674, 22681889
GO:0005515 Function Protein binding IPI 32814053
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9BQ75
Protein name Protein CMSS1 (Cms1 ribosomal small subunit homolog)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF14617 CMS1 45 275 U3-containing 90S pre-ribosomal complex subunit Family
Sequence
Sequence length 279
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
16
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
ANEMIA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ATRIAL FIBRILLATION GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
BREAST CANCER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
BREAST CARCINOMA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Breast Carcinoma Breast Carcinoma GWASCAT_DG 29059683
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Coronary heart disease Coronary Heart Disease GWASDB_DG 22751097
★☆☆☆☆
Found in Text Mining only
Severe myopia Myopia BEFREE 26485405
★☆☆☆☆
Found in Text Mining only