Gene Gene information from NCBI Gene database.
Entrez ID 113622
Gene name ADP-ribosylhydrolase like 1
Gene symbol ADPRHL1
Synonyms (NCBI Gene)
ARH2
Chromosome 13
Chromosome location 13q34
Summary ADP-ribosylation is a reversible posttranslational modification used to regulate protein function. ADP-ribosyltransferases (see ART1; MIM 601625) transfer ADP-ribose from NAD+ to the target protein, and ADP-ribosylhydrolases, such as ADPRHL1, reverse the
miRNA miRNA information provided by mirtarbase database.
61
miRTarBase ID miRNA Experiments Reference
MIRT488731 hsa-miR-3174 PAR-CLIP 23592263
MIRT488730 hsa-miR-4255 PAR-CLIP 23592263
MIRT488729 hsa-miR-4795-5p PAR-CLIP 23592263
MIRT488728 hsa-miR-1236-5p PAR-CLIP 23592263
MIRT488727 hsa-miR-4765 PAR-CLIP 23592263
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:0000287 Function Magnesium ion binding IEA
GO:0003242 Process Cardiac chamber ballooning ISS
GO:0003875 Function ADP-ribosylarginine hydrolase activity IEA
GO:0005737 Component Cytoplasm IEA
GO:0030017 Component Sarcomere IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
610620 21303 ENSG00000153531
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8NDY3
Protein name Inactive ADP-ribosyltransferase ARH2 (ADP-ribosylhydrolase-like protein 1) ([Protein ADP-ribosylarginine] hydrolase-like protein 1)
Protein function Required for myofibril assembly and outgrowth of the cardiac chambers in the developing heart (By similarity). Appears to be catalytically inactive, showing no activity against O-acetyl-ADP-ribose (By similarity). {ECO:0000250|UniProtKB:Q6AZR2,
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF03747 ADP_ribosyl_GH 6 328 ADP-ribosylglycohydrolase Family
Sequence
Sequence length 354
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
ATRIAL FIBRILLATION GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
HYPERTROPHIC CARDIOMYOPATHY GWAS catalog
★★☆☆☆
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
Carcinogenesis Carcinogenesis Pubtator 35816343 Associate
★☆☆☆☆
Found in Text Mining only
Carcinoma Hepatocellular Hepatocellular carcinoma Pubtator 38302034 Associate
★☆☆☆☆
Found in Text Mining only
Glycogen Storage Disease Type IV Glycogen storage disease Pubtator 35216615 Associate
★☆☆☆☆
Found in Text Mining only
Prostatic Neoplasms Prostatic neoplasm Pubtator 35816343 Associate
★☆☆☆☆
Found in Text Mining only
Uveal melanoma Uveal Melanoma BEFREE 29031853
★☆☆☆☆
Found in Text Mining only