Gene Gene information from NCBI Gene database.
Entrez ID 7060
Gene name Thrombospondin 4
Gene symbol THBS4
Synonyms (NCBI Gene)
TSP-4TSP4
Chromosome 5
Chromosome location 5q14.1
Summary The protein encoded by this gene belongs to the thrombospondin protein family. Thrombospondin family members are adhesive glycoproteins that mediate cell-to-cell and cell-to-matrix interactions. This protein forms a pentamer and can bind to heparin and ca
miRNA miRNA information provided by mirtarbase database.
12
miRTarBase ID miRNA Experiments Reference
MIRT1423139 hsa-miR-137 CLIP-seq
MIRT1423140 hsa-miR-181a CLIP-seq
MIRT1423141 hsa-miR-181b CLIP-seq
MIRT1423142 hsa-miR-181c CLIP-seq
MIRT1423143 hsa-miR-181d CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
37
GO ID Ontology Definition Evidence Reference
GO:0001938 Process Positive regulation of endothelial cell proliferation IDA 12952849
GO:0005178 Function Integrin binding IDA 16099885
GO:0005509 Function Calcium ion binding IDA 7852353, 16246837
GO:0005509 Function Calcium ion binding IEA
GO:0005515 Function Protein binding IPI 22682248
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
600715 11788 ENSG00000113296
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P35443
Protein name Thrombospondin-4
Protein function Adhesive glycoprotein that mediates cell-to-cell and cell-to-matrix interactions and is involved in various processes including cellular proliferation, migration, adhesion and attachment, inflammatory response to CNS injury, regulation of vascul
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF11598 COMP 218 262 Cartilage oligomeric matrix protein Family
PF07645 EGF_CA 326 377 Calcium-binding EGF domain Domain
PF07645 EGF_CA 379 422 Calcium-binding EGF domain Domain
PF02412 TSP_3 496 531 Thrombospondin type 3 repeat Repeat
PF02412 TSP_3 555 590 Thrombospondin type 3 repeat Repeat
PF02412 TSP_3 590 613 Thrombospondin type 3 repeat Repeat
PF02412 TSP_3 614 651 Thrombospondin type 3 repeat Repeat
PF02412 TSP_3 652 691 Thrombospondin type 3 repeat Repeat
PF02412 TSP_3 692 727 Thrombospondin type 3 repeat Repeat
PF05735 TSP_C 745 942 Thrombospondin C-terminal region Family
Sequence
MLAPRGAAVLLLHLVLQRWLAAGAQATPQVFDLLPSSSQRLNPGALLPVLTDPALNDLYV
ISTFKLQTKSSATIFGLYSSTDNSKYFEFTVMGRLNKAILRYLKNDGKVHLVVFNNLQLA
DGRRHRILLRLSNLQRGAGSLELYLDCIQVDSVHNLPRAFAGPSQKPETIELRTFQRKPQ
DFLEELKLVVRGSLFQVASLQDCFLQQSEPLAATGTGDFNRQFLGQMTQLNQLLGEVKDL
LRQQVKETSFLRNTIAECQACG
PLKFQSPTPSTVVPPAPPAPPTRPPRRCDSNPCFRGVQ
CTDSRDGFQCGPCPEGYTGNGITCIDVDECKYHPCYPGVHCINLSPGFRCDACPVGFTGP
MVQGVGISFAKSNKQVC
TDIDECRNGACVPNSICVNTLGSYRCGPCKPGYTGDQIRGCKA
ER
NCRNPELNPCSVNAQCIEERQGDVTCVCGVGWAGDGYICGKDVDIDSYPDEELPCSAR
NCKKDNCKYVPNSGQEDADRDGIGDACDEDADGDGILNEQDNCVLIHNVDQRNSDKDIFG
DACDNCLSVLNNDQKDTDGDGRGDACDDDMDGDGIKNILDNCPKFPNRDQRDKDGDGVGD
ACDSCPDVSNPNQ
SDVDNDLVGDSCDTNQDSDGDGHQDSTDNCPTVINSAQLDTDKDGIG
DECDDDDDNDGIPDLVPPGPDNCRLVPNPAQ
EDSNSDGVGDICESDFDQDQVIDRIDVCP
ENAEVTL
TDFRAYQTVVLDPEGDAQIDPNWVVLNQGMEIVQTMNSDPGLAVGYTAFNGVD
FEGTFHVNTQTDDDYAGFIFGYQDSSSFYVVMWKQTEQTYWQATPFRAVAEPGIQLKAVK
SKTGPGEHLRNSLWHTGDTSDQVRLLWKDSRNVGWKDKVSYRWFLQHRPQVGYIRVRFYE
GSELVADSGVTIDTTMRGGRLGVFCFSQENIIWSNLKYRCND
TIPEDFQEFQTQNFDRFD
N
Sequence length 961
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Phagosome
PI3K-Akt signaling pathway
Focal adhesion
ECM-receptor interaction
Cytoskeleton in muscle cells
Malaria
Human papillomavirus infection
  Signaling by PDGF
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
12
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
Acute myeloid leukemia Benign ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ATTENTION DEFICIT HYPERACTIVITY DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Cervical cancer Benign ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Chronic lymphocytic leukemia/small lymphocytic lymphoma Benign ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Alzheimer Disease Associate 34044860
★☆☆☆☆
Found in Text Mining only
Carcinogenesis Associate 20846368
★☆☆☆☆
Found in Text Mining only
Carcinoma Hepatocellular Associate 27769059
★☆☆☆☆
Found in Text Mining only
Carcinoma Renal Cell Associate 36232491
★☆☆☆☆
Found in Text Mining only
Cardiomyopathies Associate 32631246
★☆☆☆☆
Found in Text Mining only
Cartilage Diseases Associate 30669608
★☆☆☆☆
Found in Text Mining only
Colorectal Neoplasms Associate 20846368
★☆☆☆☆
Found in Text Mining only
Coronary Disease Associate 15121769
★☆☆☆☆
Found in Text Mining only
COVID 19 Associate 36959416
★☆☆☆☆
Found in Text Mining only
Diabetes Gestational Associate 32111749
★☆☆☆☆
Found in Text Mining only