Gene
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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8544 |
Gene nameGene Name - the full gene name approved by the HGNC.
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Pirin |
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
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PIR |
SynonymsGene synonyms aliases
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- |
ChromosomeChromosome number
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X |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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Xp22.2 |
SummarySummary of gene provided in NCBI Entrez Gene.
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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.
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Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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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
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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 |
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Sequence |
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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.
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Associated diseases
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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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