Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
64761
Gene name Gene Name - the full gene name approved by the HGNC.
Poly(ADP-ribose) polymerase family member 12
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
PARP12
Synonyms (NCBI Gene) Gene synonyms aliases
ARTD12, MST109, MSTP109, ZC3H1, ZC3HDC1
Chromosome Chromosome number
7
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
7q34
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT027561 hsa-miR-98-5p Microarray 19088304
MIRT1214444 hsa-miR-1323 CLIP-seq
MIRT1214445 hsa-miR-3654 CLIP-seq
MIRT1214446 hsa-miR-4477a CLIP-seq
MIRT1214447 hsa-miR-548a-3p CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0003723 Function RNA binding HDA 22658674
GO:0003950 Function NAD+ ADP-ribosyltransferase activity IEA
GO:0005634 Component Nucleus IEA
GO:0046872 Function Metal ion binding IEA
GO:0070213 Process Protein auto-ADP-ribosylation IDA 25043379
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
612481 21919 ENSG00000059378
Protein
UniProt ID Q9H0J9
Protein name Protein mono-ADP-ribosyltransferase PARP12 (EC 2.4.2.-) (ADP-ribosyltransferase diphtheria toxin-like 12) (ARTD12) (Poly [ADP-ribose] polymerase 12) (PARP-12) (Zinc finger CCCH domain-containing protein 1)
Protein function Mono-ADP-ribosyltransferase that mediates mono-ADP-ribosylation of target proteins (PubMed:25043379, PubMed:34969853). Acts as an antiviral factor by cooperating with PARP11 to suppress Zika virus replication (PubMed:34187568). Displays anti-alp
PDB 2PQF , 6V3W , 8XPX
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00642 zf-CCCH 177 201 Zinc finger C-x8-C-x5-C-x3-H type (and similar) Family
PF02825 WWE 377 458 WWE domain Family
PF00644 PARP 507 679 Poly(ADP-ribose) polymerase catalytic domain Family
Sequence
MAQAGVVGEVTQVLCAAGGALELPELRRRLRMGLSADALERLLRQRGRFVVAVRAGGAAA
APERVVLAASPLRLCRAHQGSKPGCVGLCAQLHLCRFMVYGACKFLRAGKNCRNSHSLTT
EHNLSVLRTHGVDHLSYNELCQLLFQNDPWLLPEICQHYNKGDGPHGSCAFQKQCIKLHI
CQYFLQGECKFGTSCKRSHDF
SNSENLEKLEKLGMSSDLVSRLPTIYRNAHDIKNKSSAP
SRVPPLFVPQGTSERKDSSGSVSPNTLSQEEGDQICLYHIRKSCSFQDKCHRVHFHLPYR
WQFLDRGKWEDLDNMELIEEAYCNPKIERILCSESASTFHSHCLNFNAMTYGATQARRLS
TASSVTKPPHFILTTDWIWYWSDEFGSWQEYGRQGTVHPVTTVSSSDVEKAYLAYCTPGS
DGQAATLKFQAGKHNYELDFKAFVQKNLVYGTTKKVCR
RPKYVSPQDVTTMQTCNTKFPG
PKSIPDYWDSSALPDPGFQKITLSSSSEEYQKVWNLFNRTLPFYFVQKIERVQNLALWEV
YQWQKGQMQKQNGGKAVDERQLFHGTSAIFVDAICQQNFDWRVCGVHGTSYGKGSYFARD
AAYSHHYSKSDTQTHTMFLARVLVGEFVRGNASFVRPPAKEGWSNAFYDSCVNSVSDPSI
FVIFEKHQVYPEYVIQYTT
SSKPSVTPSILLALGSLFSSRQ
Sequence length 701
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Coronary artery disease Coronary Artery Disease rs137852988, rs121918313, rs121918529, rs121918531, rs137852340, rs1555800701, rs1215189537 29212778
Age-related macular degeneration Age related macular degeneration rs199474657, rs61750120, rs1800728, rs62654397, rs61749423, rs61751412, rs61749439, rs61751398, rs61752417, rs62645946, rs1801269, rs62646860, rs61750142, rs61750145, rs61750152
View all (20 more)
30742112
Unknown
Disease term Disease name Evidence References Source
Vitiligo Vitiligo GWAS
Myocardial Infarction Myocardial Infarction GWAS
Associations from Text Mining
Disease Name Relationship Type References
Adenocarcinoma Associate 34514952
Carcinoma Hepatocellular Associate 38302034
Colorectal Neoplasms Associate 22194930, 28615517
Diffuse Intrinsic Pontine Glioma Associate 32229503
Drug Related Side Effects and Adverse Reactions Inhibit 26505995
Hypomagnesemia 5 Renal with Ocular Involvement Associate 26005050
Lymphoma Large B Cell Diffuse Associate 35322192
Neoplasms Associate 31408463, 35945529, 36929572
Ovarian Neoplasms Associate 36063278
Recombinant chromosome 8 syndrome Associate 36929572