Gene Gene information from NCBI Gene database.
Entrez ID 6398
Gene name Secreted and transmembrane 1
Gene symbol SECTM1
Synonyms (NCBI Gene)
K12SECTM
Chromosome 17
Chromosome location 17q25.3
Summary This gene encodes a transmembrane and secreted protein with characteristics of a type 1a transmembrane protein. It is found in a perinuclear Golgi-like pattern and thought to be involved in hematopoietic and/or immune system processes. [provided by RefSeq
miRNA miRNA information provided by mirtarbase database.
35
miRTarBase ID miRNA Experiments Reference
MIRT022533 hsa-miR-124-3p Microarray 18668037
MIRT719387 hsa-miR-181d-3p HITS-CLIP 19536157
MIRT719386 hsa-miR-6752-3p HITS-CLIP 19536157
MIRT719385 hsa-miR-6499-5p HITS-CLIP 19536157
MIRT719387 hsa-miR-181d-3p HITS-CLIP 19536157
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
21
GO ID Ontology Definition Evidence Reference
GO:0002726 Process Positive regulation of T cell cytokine production IDA 10652336
GO:0002726 Process Positive regulation of T cell cytokine production IDA 22184754
GO:0005125 Function Cytokine activity IEA
GO:0005125 Function Cytokine activity TAS 9480746
GO:0005515 Function Protein binding IPI 32296183
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
602602 10707 ENSG00000141574
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8WVN6
Protein name Secreted and transmembrane protein 1 (Protein K-12)
Protein function May be involved in thymocyte signaling.
Family and domains
Tissue specificity TISSUE SPECIFICITY: Detected at the highest levels in peripheral blood leukocytes and breast cancer cell lines. Found in leukocytes of the myeloid lineage, with the strongest expression observed in granulocytes and no detectable expression in lymphocytes.
Sequence
MQTCPLAFPGHVSQALGTLLFLAASLSAQNEGWDSPICTEGVVSVSWGENTVMSCNISNA
FSHVNIKLRAHGQESAIFNEVAPGYFSRDGWQLQVQGGVAQLVIKGARDSHAGLYMWHLV
GHQRNNRQVTLEVSGAEPQSAPDTGFWPVPAVVTAVFILLVALVMFAWYRCRCSQQRREK
KFFLLEPQMKVAALRAGAQQGLSRASAELWTPDSEPTPRPLALVFKPSPLGALELLSPQP
LFPYAADP
Sequence length 248
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
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
BENIGN THYROID GLAND NEOPLASM 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
Carcinoma Renal Cell Renal cell carcinoma Pubtator 37455213 Associate
★☆☆☆☆
Found in Text Mining only
Corneal Dystrophy, Juvenile Epithelial of Meesmann Corneal Dystrophy, Epithelial Of Meesmann BEFREE 10781519, 12084738, 9171831
★☆☆☆☆
Found in Text Mining only
Macular dystrophy, corneal type 1 Macular corneal dystrophy BEFREE 10781519
★☆☆☆☆
Found in Text Mining only
Melanoma Melanoma Pubtator 24157461 Associate
★☆☆☆☆
Found in Text Mining only