Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
58485
Gene name Gene Name - the full gene name approved by the HGNC.
Trafficking protein particle complex subunit 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
TRAPPC1
Synonyms (NCBI Gene) Gene synonyms aliases
BET5, MUM2
Chromosome Chromosome number
17
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
17p13.1
Summary Summary of gene provided in NCBI Entrez Gene.
This gene product plays a role in vesicular transport of proteins to the Golgi apparatus from the endoplasmic reticulum. The encoded protein is a component of the multisubunit transport protein particle (TRAPP) complex. Alternative splicing results in mul
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT052132 hsa-let-7b-5p CLASH 23622248
MIRT050712 hsa-miR-18a-5p CLASH 23622248
MIRT048144 hsa-miR-197-3p CLASH 23622248
MIRT046518 hsa-miR-15b-5p CLASH 23622248
MIRT036554 hsa-miR-1224-5p CLASH 23622248
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000139 Component Golgi membrane IEA
GO:0005515 Function Protein binding IPI 28514442, 32296183
GO:0005576 Component Extracellular region TAS
GO:0005783 Component Endoplasmic reticulum IEA
GO:0005829 Component Cytosol TAS
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
610969 19894 ENSG00000170043
Protein
UniProt ID Q9Y5R8
Protein name Trafficking protein particle complex subunit 1 (BET5 homolog) (Multiple myeloma protein 2) (MUM-2)
Protein function May play a role in vesicular transport from endoplasmic reticulum to Golgi.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF04099 Sybindin 3 137 Sybindin-like family Family
Sequence
Sequence length 145
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    COPII-mediated vesicle transport
Neutrophil degranulation
RAB GEFs exchange GTP for GDP on RABs
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Melanoma melanoma rs121913315, rs121913323, rs137853080, rs137853081, rs121909232, rs121913388, rs104894094, rs104894095, rs104894097, rs104894098, rs104894099, rs104894109, rs137854599, rs11547328, rs104894340
View all (64 more)
Associations from Text Mining
Disease Name Relationship Type References
Developmental Disabilities Associate 39273027
Genetic Diseases Inborn Associate 39273027
HEM dysplasia Associate 39273027
Intellectual Disability Associate 39273027
Muscular Diseases Associate 39273027
Muscular Dystrophies Associate 39273027