Gene Gene information from NCBI Gene database.
Entrez ID 54879
Gene name Suppression of tumorigenicity 7 like
Gene symbol ST7L
Synonyms (NCBI Gene)
FAM4BST7RSTLR
Chromosome 1
Chromosome location 1p13.2
Summary This gene was identified by its similarity to the ST7 tumor suppressor gene found in the chromosome 7q31 region. This gene is clustered in a tail-to-tail manner with the WNT2B gene in a chromosomal region known to be deleted and rearranged in a variety of
miRNA miRNA information provided by mirtarbase database.
114
miRTarBase ID miRNA Experiments Reference
MIRT007215 hsa-miR-24-3p Luciferase reporter assayqRT-PCRWestern blot 23142218
MIRT007215 hsa-miR-24-3p Luciferase reporter assayqRT-PCRWestern blot 23142218
MIRT040824 hsa-miR-18a-3p CLASH 23622248
MIRT488594 hsa-miR-1321 PAR-CLIP 23592263
MIRT488593 hsa-miR-4739 PAR-CLIP 23592263
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
3
GO ID Ontology Definition Evidence Reference
GO:0016020 Component Membrane IEA
GO:0030308 Process Negative regulation of cell growth IEA
GO:0030308 Process Negative regulation of cell growth ISS
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
617640 18441 ENSG00000007341
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8TDW4
Protein name Suppressor of tumorigenicity 7 protein-like (ST7-related protein)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF04184 ST7 38 555 ST7 protein Family
Sequence
Sequence length 575
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
3
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
OPEN-ANGLE GLAUCOMA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
PANCREATIC CARCINOMA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Carcinoma Ovarian Epithelial Associate 27537390
★☆☆☆☆
Found in Text Mining only
Neoplasms Associate 27537390
★☆☆☆☆
Found in Text Mining only
Pancreatic Neoplasms Associate 32924881
★☆☆☆☆
Found in Text Mining only