Gene Gene information from NCBI Gene database.
Entrez ID 11346
Gene name Synaptopodin
Gene symbol SYNPO
Synonyms (NCBI Gene)
SYNPO1
Chromosome 5
Chromosome location 5q33.1
Summary Synaptopodin is an actin-associated protein that may play a role in actin-based cell shape and motility. The name synaptopodin derives from the protein`s associations with postsynaptic densities and dendritic spines and with renal podocytes (Mundel et al.
miRNA miRNA information provided by mirtarbase database.
183
miRTarBase ID miRNA Experiments Reference
MIRT686735 hsa-miR-4311 HITS-CLIP 23313552
MIRT608417 hsa-miR-6867-5p HITS-CLIP 23313552
MIRT608416 hsa-miR-6818-5p HITS-CLIP 23313552
MIRT608415 hsa-miR-574-5p HITS-CLIP 23313552
MIRT608417 hsa-miR-6867-5p HITS-CLIP 24906430
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
31
GO ID Ontology Definition Evidence Reference
GO:0001725 Component Stress fiber IBA
GO:0003779 Function Actin binding IBA
GO:0003779 Function Actin binding IEA
GO:0003779 Function Actin binding ISS
GO:0005515 Function Protein binding IPI 15841212, 18596123, 26496610, 30021884, 31597702, 32296183
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
608155 30672 ENSG00000171992
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8N3V7
Protein name Synaptopodin
Protein function Actin-associated protein that may play a role in modulating actin-based shape and motility of dendritic spines and renal podocyte foot processes. Seems to be essential for the formation of spine apparatuses in spines of telencephalic neurons, wh
Family and domains
Tissue specificity TISSUE SPECIFICITY: Expressed in cerebral cortex. {ECO:0000269|PubMed:9314539}.
Sequence
MLGPHLPPPPLAPSEGRPTPCAFQIPDGSYRCLALEAEESSGEEGLQGEVGPTDLEEDEG
VSRSGDDSACRVTQGTPQLPKALGIQPPSCSREEQGASQHDDRASQDWDVVKAGQMMTAS
PSPGPGPRVAQKPALGRSTSLTEKDLKEAKARSQQIAAQLTTPPSSNSRGVQLFNRRRQR
VNEFTLESHGQRGQKPSQESLRVLPSSLPGHAPGLSLSSTSLPEPGPPRHPSPQSPDRGV
PGHSMEGYSEEASLLRHLEKVASEEEEVPLVVYLKENAALLTANGLHLSQNREAQQSSPA
PPPAEVHSPAADVNQNLASPSATLTTPTSNSSHNPPATDVNQNPPATVVPQSLPLSSIQQ
NSSEAQLPSNGTGPASKPSTLCADGQPQAPAEEVRCSTLLIDKVSTPATTTSTFSREATL
IPSSRPPASDFMSSSLLIDIQPNTLVVSADQEMSGRAAATTPTKVYSEVHFTLAKPPSVV
NRTARPFGIQAPGGTSQMERSPMLERRHFGEKAPAPQPPSLPDRSPRPQRHIMSRSPMVE
RRMMGQRSPASERRPLGNFTAPPTYTETLSTAPLASWVRSPPSYSVLYPSSDPKSSHLKG
QAVPASKTGILEESMARRGSRKSMFTFVEKPKVTPNPDLLDLVQTADEKRRQRDQGEVGV
EEEPFALGAEASNFQQEPAPRDRASPAAAEEVVPEWASCLKSPRIQAKPKPKPNQNLSEA
SGKGAELYARRQSRMEKYVIESSSHTPELARCPSPTMSLPSSWKYPTNAPGAFRVASRSP
ARTPPASLYHGYLPENGVLRPEPTKQPPYQLRPSLFVLSPIKEPAKVSPRAASPAKPSSL
DLVPNLPKGALPPSPALPRPSRSSPGLYTSPGQDSLQPTAVSPPYGGDISPVSPSRAWSP
RAKQAPRPSFSTRNAGIEAQVWKPSFCFK
Sequence length 929
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG 
  Tight junction  
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
13
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Cervical cancer Benign rs61741920 RCV005911647
Cholangiocarcinoma Benign rs59962087, rs61741920 RCV005922022
RCV005911650
Clear cell carcinoma of kidney Uncertain significance; Benign rs41336050, rs61741920 RCV005930640
RCV005911648
Familial pancreatic carcinoma Benign rs59962087 RCV005922021
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Autism Spectrum Disorder Associate 31254375
Carcinoma Squamous Cell Associate 32991423
Cicatrix Associate 20370455
Cognitive Dysfunction Inhibit 30372675
Diabetic Nephropathies Associate 21655212, 22629296, 35637650
Diabetic Nephropathies Inhibit 22615747
Drug Hypersensitivity Associate 33318199
Eosinophilic Esophagitis Associate 29046486
Glomerulosclerosis Focal Segmental Associate 11135064, 18336100
Inflammation Stimulate 29046486