Gene Gene information from NCBI Gene database.
Entrez ID 100128327
Gene name Trafficking protein particle complex subunit 3L
Gene symbol TRAPPC3L
Synonyms (NCBI Gene)
BET3LbA259P20.2
Chromosome 6
Chromosome location 6q22.1
miRNA miRNA information provided by mirtarbase database.
30
miRTarBase ID miRNA Experiments Reference
MIRT717870 hsa-miR-216b-3p HITS-CLIP 19536157
MIRT717869 hsa-miR-1293 HITS-CLIP 19536157
MIRT717868 hsa-miR-4483 HITS-CLIP 19536157
MIRT652237 hsa-miR-4301 HITS-CLIP 23824327
MIRT652236 hsa-miR-4324 HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
12
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 21525244
GO:0005783 Component Endoplasmic reticulum IEA
GO:0005794 Component Golgi apparatus IEA
GO:0005829 Component Cytosol IBA
GO:0006888 Process Endoplasmic reticulum to Golgi vesicle-mediated transport IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
614137 21090 ENSG00000173626
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q5T215
Protein name Trafficking protein particle complex subunit 3-like protein (TRAPPC3-like protein) (BET3-like protein)
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
PF04051 TRAPP 19 167 Transport protein particle (TRAPP) component Family
Sequence
Sequence length 181
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
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
NEPHROTIC SYNDROME GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
PELVIC ORGAN PROLAPSE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations