Gene Gene information from NCBI Gene database.
Entrez ID 286319
Gene name Tumor suppressor candidate 1
Gene symbol TUSC1
Synonyms (NCBI Gene)
CCDC89BTSG-9TSG9
Chromosome 9
Chromosome location 9p21.2
Summary This gene is located within the region of chromosome 9p that harbors tumor suppressor genes critical in carcinogenesis. It is an intronless gene which is downregulated in non-small-cell lung cancer and small-cell lung cancer cell lines, suggesting that it
miRNA miRNA information provided by mirtarbase database.
132
miRTarBase ID miRNA Experiments Reference
MIRT025062 hsa-miR-181a-5p Microarray 17612493
MIRT504320 hsa-miR-3529-3p PAR-CLIP 20371350
MIRT504319 hsa-miR-4700-3p PAR-CLIP 20371350
MIRT504318 hsa-miR-3148 PAR-CLIP 20371350
MIRT504317 hsa-miR-4668-5p PAR-CLIP 20371350
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
610529 31010 ENSG00000198680
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q2TAM9
Protein name Tumor suppressor candidate gene 1 protein (TSG-9) (TSG9)
Family and domains
Tissue specificity TISSUE SPECIFICITY: Widely expressed at low level. Expressed at higher level in testis, weakly expressed in muscle, colon, lung and spleen. Not detected in 3 non small cell lung carcinoma (NSCLC) cell lines with homozygous deletion of the 9p region, while
Sequence
MGPMWRMRGGATRRGSCCGGDGAADGRGPGRSGRARGGGSPSGGGGGVGWRGRADGARQQ
LEERFADLAASHLEAIRARDEWDRQNARLRQENARLRLENRRLKRENRSLFRQALRLPGE
GGNGTPAEARRVPEEASTNRRARDSGREDEPGSPRALRARLEKLEAMYRRALLQLHLEQR
GPRPSGDKEEQPLQEPDSGLRSRDSEPSGPWL
Sequence length 212
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
11
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
ALZHEIMER DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ANXIETY DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ATTENTION DEFICIT HYPERACTIVITY DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
BIPOLAR DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Azoospermia Associate 28975488
★☆☆☆☆
Found in Text Mining only
Breast Neoplasms Associate 35655316
★☆☆☆☆
Found in Text Mining only
Infertility Male Associate 28975488
★☆☆☆☆
Found in Text Mining only
Leukemia Myelogenous Chronic BCR ABL Positive Associate 40503228
★☆☆☆☆
Found in Text Mining only
Neoplasms Associate 35655316
★☆☆☆☆
Found in Text Mining only
Oligospermia Associate 28975488
★☆☆☆☆
Found in Text Mining only
Urinary Bladder Neoplasms Associate 25239644
★☆☆☆☆
Found in Text Mining only