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

Gene Gene information from NCBI Gene database.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Entrez ID 780776
Gene name Trans-golgi network vesicle protein 23 homolog A
Gene symbol TVP23A
Synonyms (NCBI Gene)
FAM18AYDR084C
Chromosome 16
Chromosome location 16p13.13
Summary 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.
11
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 (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
5
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 identifiers for this gene in OMIM, HGNC, and Ensembl databases.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
Gene miRNA Gene ontology Other IDs Protein Associated diseases
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)
Show/Hide Unknown Diseases (1)
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
OLIGODENDROGLIOMA — GWAS catalog
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Show/Hide Text Mining Associations (1)
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Parkinson Disease Associate 34148545
★★★★★
★☆☆☆☆
Found in Text Mining only