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PIR (pirin)

Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
8544
Gene nameGene Name - the full gene name approved by the HGNC.
Pirin
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
PIR
SynonymsGene synonyms aliases
-
ChromosomeChromosome number
X
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
Xp22.2
SummarySummary of gene provided in NCBI Entrez Gene.
This gene encodes a member of the cupin superfamily. The encoded protein is an Fe(II)-containing nuclear protein expressed in all tissues of the body and concentrated within dot-like subnuclear structures. Interactions with nuclear factor I/CCAAT box tran
miRNAmiRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT023859 hsa-miR-1-3p Proteomics 18668040
Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0003712 Function Transcription coregulator activity IMP 23716661
GO:0005515 Function Protein binding IPI 10362352
GO:0005634 Component Nucleus IBA 21873635
GO:0005634 Component Nucleus IDA 9079676
GO:0005654 Component Nucleoplasm TAS
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM
HGNC
e!Ensembl
Protein
UniProt ID O00625
Protein name Pirin (EC 1.13.11.24) (Probable quercetin 2,3-dioxygenase PIR) (Probable quercetinase)
Protein function Transcriptional coregulator of NF-kappa-B which facilitates binding of NF-kappa-B proteins to target kappa-B genes in a redox-state-dependent manner. May be required for efficient terminal myeloid maturation of hematopoietic cells. Has quercetin
PDB 1J1L , 3ACL , 4ERO , 4EWA , 4EWD , 4EWE , 4GUL , 4HLT , 5JCT , 6H1H , 6H1I , 6N0J , 6N0K
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF02678 Pirin
21 118
Pirin
Family
PF05726 Pirin_C
171 277
Pirin C-terminal cupin domain
Domain
Sequence
Sequence length 290
Interactions View interactions
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
 
Reactome
    Digestion
Associated diseases
Causal
Disease name Disease term dbSNP ID References
Dermatitis Contact Dermatitis rs61816761, rs150597413, rs138726443, rs201356558, rs149484917, rs372754256, rs747301529, rs567795279, rs745915174 25724174
Osteoporosis Osteoporosis rs72658152, rs72667023, rs587776916, rs72656370, rs768615287 19766747

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