TVP23A (trans-golgi network vesicle protein 23 homolog A)

Gene
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
780776
Gene name Gene Name - the full gene name approved by the HGNC.
Trans-golgi network vesicle protein 23 homolog A
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
TVP23A
Synonyms (NCBI Gene) Gene synonyms aliases
FAM18A, YDR084C
Chromosome Chromosome number
16
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
16p13.13
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a membrane protein associated with the Golgi apparatus, which plays a crucial role in intracellular vesicular transport. The encoded protein is likely associated with the late (trans) Golgi compartments, which are involved in the deliver
miRNA miRNA information provided by mirtarbase database.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide all(11)
miRTarBase ID miRNA Experiments Reference
MIRT017198 hsa-miR-335-5p Microarray 18185580
MIRT513170 hsa-miR-651-3p PAR-CLIP 23446348
MIRT513169 hsa-miR-4496 PAR-CLIP 23446348
MIRT513168 hsa-miR-219b-5p PAR-CLIP 23446348
MIRT513166 hsa-miR-4261 PAR-CLIP 23446348
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide all(5)
GO ID Ontology Definition Evidence Reference
GO:0000139 Component Golgi membrane IBA
GO:0005515 Function Protein binding IPI 32296183
GO:0009306 Process Protein secretion IBA
GO:0016020 Component Membrane IEA
GO:0016192 Process Vesicle-mediated transport IBA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein
Gene miRNA Gene ontology Other IDs Protein Associated diseases
UniProt ID A6NH52
Protein name Golgi apparatus membrane protein TVP23 homolog A
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF05832 DUF846 30 → 171 Eukaryotic protein of unknown function (DUF846) Family
Sequence
Sequence length 213
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)
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide Unknown Diseases (1)
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
Oligodendroglioma Oligodendroglioma N/A N/A GWAS
Show/Hide Text Mining Associations (1)
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Parkinson Disease Associate 34148545