Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
6447
Gene name Gene Name - the full gene name approved by the HGNC.
Secretogranin V
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SCG5
Synonyms (NCBI Gene) Gene synonyms aliases
7B2, P7B2, SGNE1, SgV
Chromosome Chromosome number
15
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
15q13.3
Summary Summary of gene provided in NCBI Entrez Gene.
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.
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 information of associated ontologies with gene provided by GO database.
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 ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
173120 10816 ENSG00000166922
Protein
UniProt ID 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
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Colorectal Cancer Colorectal cancer, ICD10 C18, C19, C20: colorectal cancer, Colorectal cancer (PheCode 153) N/A N/A GWAS
Hereditary Mixed Polyposis Syndrome hereditary mixed polyposis syndrome N/A N/A ClinVar
Associations from Text Mining Disease 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