Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
10417
Gene name Gene Name - the full gene name approved by the HGNC.
Spondin 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SPON2
Synonyms (NCBI Gene) Gene synonyms aliases
DIL-1, DIL1, M-SPONDIN, MINDIN
Chromosome Chromosome number
4
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
4p16.3
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT021428 hsa-miR-9-5p Microarray 17612493
MIRT755466 hsa-miR-328-5p Luciferase reporter assay, Western blotting, qRT-PCR, Immunoprecipitaion (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 information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 25416956, 32296183, 32814053
GO:0007155 Process Cell adhesion IBA 21873635
GO:0031012 Component Extracellular matrix IBA 21873635
GO:0045087 Process Innate immune response IEA
GO:0046872 Function Metal ion binding IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
605918 11253 ENSG00000159674
Protein
UniProt ID 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 information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Prostate cancer Malignant neoplasm of prostate rs121909139, rs121909140, rs121909141, rs121909142, rs121909143, rs606231169, rs606231170, rs137852584, rs137852578, rs137852580, rs137852581, rs137852582 19208208
Associations from Text Mining
Disease Name Relationship Type References
Adenoma Associate 30175151
Asthma Associate 33998076
Atherosclerosis Inhibit 39941136
Carcinogenesis Associate 37713832
Carcinoma Hepatocellular Associate 17006932
Carcinoma Hepatocellular Stimulate 30318967
Carcinoma Renal Cell Stimulate 32952742
Cardiovascular Diseases Associate 39941136
Colorectal Neoplasms Stimulate 25945835
Constriction Pathologic Associate 39941136