Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
645
Gene name Gene Name - the full gene name approved by the HGNC.
Biliverdin reductase B
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
BLVRB
Synonyms (NCBI Gene) Gene synonyms aliases
BVRB, FLR, HEL-S-10, SDR43U1
Chromosome Chromosome number
19
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
19q13.2
Summary Summary of gene provided in NCBI Entrez Gene.
The final step in heme metabolism in mammals is catalyzed by the cytosolic biliverdin reductase enzymes A and B (EC 1.3.1.24).[supplied by OMIM, Jul 2009]
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT029434 hsa-miR-26b-5p Microarray 19088304
MIRT732044 hsa-miR-127-5p Immunofluorescence, Luciferase reporter assay, qRT-PCR, Western blot 26708147
MIRT732044 hsa-miR-127-5p Immunofluorescence, Luciferase reporter assay, qRT-PCR, Western blot 26708147
MIRT822194 hsa-miR-137 CLIP-seq
MIRT822195 hsa-miR-24 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0004074 Function Biliverdin reductase (NAD(P)+) activity IDA 7929092
GO:0005515 Function Protein binding IPI 32296183
GO:0005654 Component Nucleoplasm IDA
GO:0005829 Component Cytosol IDA 7929092
GO:0005829 Component Cytosol TAS
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
600941 1063 ENSG00000090013
Protein
UniProt ID P30043
Protein name Flavin reductase (NADPH) (FR) (EC 1.5.1.30) (Biliverdin reductase B) (BVR-B) (EC 1.3.1.-) (Biliverdin-IX beta-reductase) (Green heme-binding protein) (GHBP) (NADPH-dependent diaphorase) (NADPH-flavin reductase) (FLR) (S-nitroso-CoA-assisted nitrosyltransf
Protein function Enzyme that can both act as a NAD(P)H-dependent reductase and a S-nitroso-CoA-dependent nitrosyltransferase (PubMed:10620517, PubMed:18241201, PubMed:27207795, PubMed:38056462, PubMed:7929092). Promotes fetal heme degradation during development
PDB 1HDO , 1HE2 , 1HE3 , 1HE4 , 1HE5 , 5OOG , 5OOH , 6OPL , 7ER6 , 7ER7 , 7ER8 , 7ER9 , 7ERA , 7ERB , 7ERC , 7ERD , 7ERE , 8ELL , 8ELM , 8K4K
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF13460 NAD_binding_10 10 192 NAD(P)H-binding Domain
Tissue specificity TISSUE SPECIFICITY: Predominantly expressed in liver and erythrocytes (PubMed:7929092). At lower levels in heart, lung, adrenal gland and cerebrum (PubMed:7929092). Expressed in adult red blood cells (PubMed:29932944). {ECO:0000269|PubMed:29932944, ECO:00
Sequence
Sequence length 206
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Riboflavin metabolism
Porphyrin metabolism
Metabolic pathways
  Heme degradation
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Esophagus neoplasm Squamous cell carcinoma of esophagus rs28934578, rs121918714, rs1567556006, rs1575166666 21517111
Gastric cancer Hereditary Diffuse Gastric Cancer rs137854571, rs63751108, rs34612342, rs121908383, rs121909144, rs121909775, rs121909219, rs121909223, rs63750871, rs80359530, rs121964873, rs121913530, rs606231203, rs121918505, rs587776802
View all (244 more)
19424620
Associations from Text Mining
Disease Name Relationship Type References
Atherosclerosis Associate 32653974
Carcinoma Hepatocellular Associate 26708147
Cerebral Infarction Associate 32653974
Esophageal Squamous Cell Carcinoma Associate 21517111
Intracranial Arteriosclerosis Associate 32653974
Otitis Media Associate 27632927
Thrombocytosis Associate 27207795