Gene Gene information from NCBI Gene database.
Entrez ID 8774
Gene name NSF attachment protein gamma
Gene symbol NAPG
Synonyms (NCBI Gene)
GAMMASNAP
Chromosome 18
Chromosome location 18p11.22
Summary This gene encodes soluble NSF attachment protein gamma. The soluble NSF attachment proteins (SNAPs) enable N-ethyl-maleimide-sensitive fusion protein (NSF) to bind to target membranes. NSF and SNAPs appear to be general components of the intracellular mem
miRNA miRNA information provided by mirtarbase database.
961
miRTarBase ID miRNA Experiments Reference
MIRT005148 hsa-miR-30a-5p pSILAC 18668040
MIRT001439 hsa-miR-16-5p pSILAC 18668040
MIRT005148 hsa-miR-30a-5p Proteomics;Other 18668040
MIRT001439 hsa-miR-16-5p Proteomics;Other 18668040
MIRT043705 hsa-miR-342-3p CLASH 23622248
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
17
GO ID Ontology Definition Evidence Reference
GO:0005483 Function Soluble NSF attachment protein activity IBA
GO:0005515 Function Protein binding IPI 11278501
GO:0005739 Component Mitochondrion IDA 11278501
GO:0005765 Component Lysosomal membrane HDA 17897319
GO:0005794 Component Golgi apparatus IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
603216 7642 ENSG00000134265
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q99747
Protein name Gamma-soluble NSF attachment protein (SNAP-gamma) (N-ethylmaleimide-sensitive factor attachment protein gamma)
Protein function Required for vesicular transport between the endoplasmic reticulum and the Golgi apparatus.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF14938 SNAP 7 261 Domain
Sequence
Sequence length 312
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    COPII-mediated vesicle transport
COPI-mediated anterograde transport
COPI-dependent Golgi-to-ER retrograde traffic
Intra-Golgi traffic
Retrograde transport at the Trans-Golgi-Network
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
BIPOLAR DISORDER Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Bipolar Disorder Bipolar Disorder BEFREE 16395123, 19429185
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Bipolar Disorder Bipolar Disorder PSYGENET_DG 16395123, 17239033, 19429185
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Frontotemporal dementia Frontotemporal dementia BEFREE 24095276
★☆☆☆☆
Found in Text Mining only
Osteoporosis Osteoporosis Pubtator 40603950 Associate
★☆☆☆☆
Found in Text Mining only
Pick Disease of the Brain Pica BEFREE 24095276
★☆☆☆☆
Found in Text Mining only
Retinoblastoma Retinoblastoma BEFREE 29073720
★☆☆☆☆
Found in Text Mining only
Telangiectasia Hereditary Hemorrhagic Hereditary hemorrhagic telangiectasia Pubtator 34112136 Associate
★☆☆☆☆
Found in Text Mining only