Gene Gene information from NCBI Gene database.
Entrez ID 53635
Gene name PTOV1 extended AT-hook containing adaptor protein
Gene symbol PTOV1
Synonyms (NCBI Gene)
ACID2PTOV-1
Chromosome 19
Chromosome location 19q13.33
Summary This gene encodes a protein that was found to be overexpressed in prostate adenocarcinomas. The encoded protein was found to interact with the lipid raft protein flotillin-1 and shuttle it from the cytoplasm to the nucleus in a cell cycle dependent manner
miRNA miRNA information provided by mirtarbase database.
45
miRTarBase ID miRNA Experiments Reference
MIRT045949 hsa-miR-125b-5p CLASH 23622248
MIRT044008 hsa-miR-378a-5p CLASH 23622248
MIRT1273766 hsa-miR-1288 CLIP-seq
MIRT1273767 hsa-miR-3144-5p CLIP-seq
MIRT1273768 hsa-miR-3189-3p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
8
GO ID Ontology Definition Evidence Reference
GO:0005634 Component Nucleus IEA
GO:0005654 Component Nucleoplasm IDA
GO:0005667 Component Transcription regulator complex IBA
GO:0005737 Component Cytoplasm IEA
GO:0005886 Component Plasma membrane IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
610195 9632 ENSG00000104960
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q86YD1
Protein name Prostate tumor-overexpressed gene 1 protein (PTOV-1) (Activator interaction domain-containing protein 2)
Protein function May activate transcription. Required for nuclear translocation of FLOT1. Promotes cell proliferation.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF11232 Med25 89 238 Mediator complex subunit 25 PTOV activation and synapsin 2 Domain
PF11232 Med25 254 399 Mediator complex subunit 25 PTOV activation and synapsin 2 Domain
Tissue specificity TISSUE SPECIFICITY: Expressed in brain, heart, kidney, liver, placenta, skeletal muscle and small intestine. {ECO:0000269|PubMed:11313889}.
Sequence
Sequence length 416
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
Long QT syndrome Likely benign ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
STOMACH NEOPLASMS CTD
★★☆☆☆
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
Adenocarcinoma Adenocarcinoma BEFREE 11313889
★☆☆☆☆
Found in Text Mining only
Adenocarcinoma of lung (disorder) Lung adenocarcinoma BEFREE 9219564
★☆☆☆☆
Found in Text Mining only
Anaplasia Anaplasia BEFREE 26746655
★☆☆☆☆
Found in Text Mining only
Arteriosclerosis Arteriosclerosis BEFREE 16639697
★☆☆☆☆
Found in Text Mining only
Atherosclerosis Atherosclerosis BEFREE 16639697
★☆☆☆☆
Found in Text Mining only
Atrophy Atrophy Pubtator 22507319 Associate
★☆☆☆☆
Found in Text Mining only
Autoimmune Diseases Autoimmune Diseases BEFREE 28587079
★☆☆☆☆
Found in Text Mining only
Benign Prostatic Hyperplasia Benign Prostatic Hyperplasia BEFREE 11313889
★☆☆☆☆
Found in Text Mining only
Bipolar Disorder Bipolar Disorder BEFREE 17448293
★☆☆☆☆
Found in Text Mining only
Breast Carcinoma Breast Carcinoma BEFREE 24947166, 27060981, 28160860, 30922918
★☆☆☆☆
Found in Text Mining only