Gene Gene information from NCBI Gene database.
Entrez ID 57097
Gene name Poly(ADP-ribose) polymerase family member 11
Gene symbol PARP11
Synonyms (NCBI Gene)
ARTD11C12orf6MIB006
Chromosome 12
Chromosome location 12p13.32
miRNA miRNA information provided by mirtarbase database.
315
miRTarBase ID miRNA Experiments Reference
MIRT018797 hsa-miR-335-5p Microarray 18185580
MIRT023350 hsa-miR-122-5p Microarray 17612493
MIRT025916 hsa-miR-7-5p Microarray 17612493
MIRT050051 hsa-miR-26b-5p CLASH 23622248
MIRT526867 hsa-miR-132-3p PAR-CLIP 22012620
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
26
GO ID Ontology Definition Evidence Reference
GO:0003950 Function NAD+ poly-ADP-ribosyltransferase activity IBA
GO:0003950 Function NAD+ poly-ADP-ribosyltransferase activity IDA 25673562
GO:0003950 Function NAD+ poly-ADP-ribosyltransferase activity IEA
GO:0005515 Function Protein binding IPI 32296183, 32814053
GO:0005634 Component Nucleus IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
616706 1186 ENSG00000111224
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9NR21
Protein name Protein mono-ADP-ribosyltransferase PARP11 (EC 2.4.2.-) (ADP-ribosyltransferase diphtheria toxin-like 11) (ARTD11) (Poly [ADP-ribose] polymerase 11) (PARP-11)
Protein function Mono-ADP-ribosyltransferase that mediates mono-ADP-ribosylation of target proteins (PubMed:25043379, PubMed:25673562). Plays a role in nuclear envelope stability and nuclear remodeling during spermiogenesis (By similarity). Inhibits the type I i
PDB 2DK6
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF02825 WWE 34 106 WWE domain Family
PF00644 PARP 147 338 Poly(ADP-ribose) polymerase catalytic domain Family
Sequence
Sequence length 338
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
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
SECONDARY MALIGNANT NEOPLASM 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
Cryptorchidism Cryptorchidism Pubtator 40454210 Associate
★☆☆☆☆
Found in Text Mining only
Microcephaly Microcephaly BEFREE 24780630
★☆☆☆☆
Found in Text Mining only