Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
113178
Gene name Gene Name - the full gene name approved by the HGNC.
Secretory carrier membrane protein 4
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SCAMP4
Synonyms (NCBI Gene) Gene synonyms aliases
SCAMP-4
Chromosome Chromosome number
19
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
19p13.3
Summary Summary of gene provided in NCBI Entrez Gene.
Secretory carrier membrane proteins (SCAMPs) are widely distributed integral membrane proteins implicated in membrane trafficking. Most SCAMPs (e.g., SCAMP1; MIM 606911) have N-terminal cytoplasmic NPF (arg-pro-phe) repeats, 4 central transmembrane region
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT041297 hsa-miR-193b-3p CLASH 23622248
MIRT036439 hsa-miR-1226-3p CLASH 23622248
MIRT699849 hsa-miR-548c-3p HITS-CLIP 23313552
MIRT699848 hsa-miR-6849-3p HITS-CLIP 23313552
MIRT699847 hsa-miR-3190-5p HITS-CLIP 23313552
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 32296183, 32814053
GO:0006887 Process Exocytosis IBA
GO:0015031 Process Protein transport IEA
GO:0016020 Component Membrane IEA
GO:0032588 Component Trans-Golgi network membrane IBA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
613764 30385 ENSG00000227500
Protein
UniProt ID Q969E2
Protein name Secretory carrier-associated membrane protein 4 (Secretory carrier membrane protein 4)
Protein function Probably involved in membrane protein trafficking.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF04144 SCAMP 5 179 SCAMP family Family
Sequence
Sequence length 229
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
Alzheimer disease Alzheimer's disease or family history of Alzheimer's disease N/A N/A GWAS
Diabetes Severe insulin-deficient type 2 diabetes N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Carcinogenesis Associate 34426610
Leukemia Myeloid Acute Associate 34426610
Leukemia T Cell Associate 34426610
Pancreatic Neoplasms Stimulate 33493138