Gene Gene information from NCBI Gene database.
Entrez ID 10417
Gene name Spondin 2
Gene symbol SPON2
Synonyms (NCBI Gene)
DIL-1DIL1M-SPONDINMINDIN
Chromosome 4
Chromosome location 4p16.3
miRNA miRNA information provided by mirtarbase database.
126
miRTarBase ID miRNA Experiments Reference
MIRT021428 hsa-miR-9-5p Microarray 17612493
MIRT755466 hsa-miR-328-5p Luciferase reporter assayWestern blottingqRT-PCRImmunoprecipitaion (IP)In situ hybridization 36153414
MIRT1385173 hsa-let-7a CLIP-seq
MIRT1385174 hsa-let-7b CLIP-seq
MIRT1385175 hsa-let-7c CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
25
GO ID Ontology Definition Evidence Reference
GO:0001530 Function Lipopolysaccharide binding IEA
GO:0002376 Process Immune system process IEA
GO:0002448 Process Mast cell mediated immunity IEA
GO:0003823 Function Antigen binding IEA
GO:0005515 Function Protein binding IPI 25416956, 32296183, 32814053
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
605918 11253 ENSG00000159674
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9BUD6
Protein name Spondin-2 (Differentially expressed in cancerous and non-cancerous lung cells 1) (DIL-1) (Mindin)
Protein function Cell adhesion protein that promotes adhesion and outgrowth of hippocampal embryonic neurons. Binds directly to bacteria and their components and functions as an opsonin for macrophage phagocytosis of bacteria. Essential in the initiation of the
PDB 3D34
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF06468 Spond_N 41 235 Spondin_N Domain
PF19028 TSP1_spondin 278 330 Spondin-like TSP1 domain Domain
Tissue specificity TISSUE SPECIFICITY: Expressed in normal lung tissue but not in lung carcinoma cell lines. {ECO:0000269|PubMed:10512675}.
Sequence
Sequence length 331
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Defective B3GALTL causes Peters-plus syndrome (PpS)
O-glycosylation of TSR domain-containing proteins
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
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
CARCINOMA, BASAL CELL CTD
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
PROSTATIC NEOPLASMS CTD
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Adenoma Associate 30175151
★☆☆☆☆
Found in Text Mining only
Asthma Associate 33998076
★☆☆☆☆
Found in Text Mining only
Atherosclerosis Inhibit 39941136
★☆☆☆☆
Found in Text Mining only
Carcinogenesis Associate 37713832
★☆☆☆☆
Found in Text Mining only
Carcinoma Hepatocellular Associate 17006932
★☆☆☆☆
Found in Text Mining only
Carcinoma Hepatocellular Stimulate 30318967
★☆☆☆☆
Found in Text Mining only
Carcinoma Renal Cell Stimulate 32952742
★☆☆☆☆
Found in Text Mining only
Cardiovascular Diseases Associate 39941136
★☆☆☆☆
Found in Text Mining only
Colorectal Neoplasms Stimulate 25945835
★☆☆☆☆
Found in Text Mining only
Constriction Pathologic Associate 39941136
★☆☆☆☆
Found in Text Mining only