Gene Gene information from NCBI Gene database.
Entrez ID 6447
Gene name Secretogranin V
Gene symbol SCG5
Synonyms (NCBI Gene)
7B2P7B2SGNE1SgV
Chromosome 15
Chromosome location 15q13.3
Summary This gene encodes a secreted chaperone protein that prevents the aggregation of other secreted proteins, including proteins that are associated with neurodegenerative and metabolic disease. The encoded protein may be best known for its role in the traffic
miRNA miRNA information provided by mirtarbase database.
17
miRTarBase ID miRNA Experiments Reference
MIRT1329336 hsa-miR-1911 CLIP-seq
MIRT1329337 hsa-miR-3140-3p CLIP-seq
MIRT1329338 hsa-miR-376a CLIP-seq
MIRT1329339 hsa-miR-376b CLIP-seq
MIRT1329340 hsa-miR-4268 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
18
GO ID Ontology Definition Evidence Reference
GO:0004857 Function Enzyme inhibitor activity IEA
GO:0004857 Function Enzyme inhibitor activity ISS
GO:0005515 Function Protein binding IPI 7913882, 25416956, 32296183
GO:0005525 Function GTP binding TAS 3134253
GO:0005576 Component Extracellular region IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
173120 10816 ENSG00000166922
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P05408
Protein name Neuroendocrine protein 7B2 (Pituitary polypeptide) (Secretogranin V) (Secretogranin-5) (Secretory granule endocrine protein I) [Cleaved into: N-terminal peptide; C-terminal peptide]
Protein function Acts as a molecular chaperone for PCSK2/PC2, preventing its premature activation in the regulated secretory pathway. Binds to inactive PCSK2 in the endoplasmic reticulum and facilitates its transport from there to later compartments of the secre
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF05281 Secretogranin_V 21 161 Neuroendocrine protein 7B2 precursor (Secretogranin V) Family
Sequence
Sequence length 212
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
3
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Hereditary mixed polyposis syndrome Uncertain significance rs200799739 RCV000415665
Thyroid cancer, nonmedullary, 1 Likely benign rs35500536 RCV005920788
Uterine corpus endometrial carcinoma Likely benign rs35500536 RCV005920789
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Amyotrophic Lateral Sclerosis Associate 16313519
Colorectal Neoplasms Associate 33976257
Glucose Intolerance Associate 17617923
Insulin Resistance Associate 17617923
Neoplasms Associate 16293189, 35361846
Neuroblastoma Associate 25811241
Obesity Associate 17617923
Pancreatic Neoplasms Associate 33164330
Squamous Cell Carcinoma of Head and Neck Associate 33892811
Thyroid Neoplasms Associate 27776138