BLVRB
Flavin reductase (NADPH)
Also known as: BLVRB_HUMAN, FLR, SDR43U1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P30043
- Gene
- BLVRB
- Ensembl
- ENSG00000090013
- Chromosome
- 19
- Canonical length
- 206 aa
- Protein class
- Enzymes, FDA approved drug targets, Metabolic proteins, Plasma proteins, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Vesicles,Plasma membrane,Cytosol
OverviewNCBI Gene
Enables biliverdin reductase [NAD(P)+] activity; peptidyl-cysteine S-nitrosylase activity; and riboflavin reductase (NADPH) activity. Involved in heme catabolic process; megakaryocyte differentiation; and negative regulation of insulin receptor signaling pathway. Located in cytosol; nucleoplasm; and plasma membrane. Is active in cytoplasm. [provided by Alliance of Genome Resources, Apr 2025]
Canonical amino-acid sequenceUniProt
206 residues, UniProt reviewed canonical sequence.
>P30043|BLVRB
1 MAVKKIAIFG ATGQTGLTTL AQAVQAGYEV TVLVRDSSRL PSEGPRPAHV VVGDVLQAAD
61 VDKTVAGQDA VIVLLGTRND LSPTTVMSEG ARNIVAAMKA HGVDKVVACT SAFLLWDPTK
121 VPPRLQAVTD DHIRMHKVLR ESGLKYVAVM PPHIGDQPLT GAYTVTLDGR GPSRVISKHD
181 LGHFMLRCLT TDEYDGHSTY PSHQYQLocalizationUniProt · AlphaFold · HPA
Whether an antibody against BLVRB can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.26
- Highest tissue expression
- 589 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 589 nTPM
- liver: 279 nTPM
- skeletal muscle: 214 nTPM
- esophagus: 198 nTPM
- spleen: 175 nTPM
- stomach: 142 nTPM
Single-cell type
- esophageal apical cells: 3,709 nCPM
- hofbauer cells: 2,026 nCPM
- erythrocyte progenitors: 1,710 nCPM
- enterocytes: 925 nCPM
- erythrocytes: 922 nCPM
- kupffer cells: 873 nCPM
Immune cell
- classical monocyte: 466 nTPM
- myeloid DC: 344 nTPM
- total PBMC: 260 nTPM
- intermediate monocyte: 221 nTPM
- non-classical monocyte: 118 nTPM
- plasmacytoid DC: 76 nTPM
Brain region
- pons: 56 nTPM
- medulla oblongata: 48 nTPM
- white matter: 46 nTPM
- thalamus: 44 nTPM
- choroid plexus: 43 nTPM
- spinal cord: 39 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 1.76
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.45
- DepMap mean gene effect
- 0.01
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- heme catabolic process
- megakaryocyte differentiation
- negative regulation of insulin receptor signaling pathway
Molecular functions
- biliverdin reductase [NAD(P)H] activity
- peptidyl-cysteine S-nitrosylase activity
- FMN reductase (NADH) activity
- FMN reductase (NADPH) activity
- riboflavin reductase (NADPH) activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
- NAD(P)-binding domain
- NAD(P)-binding domain superfamily
- NAD(P)H-binding
- Polyketide Oxidoreductase-like
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads BLVRB as an antibody target. Whether an autoantibody or antibody against BLVRB could matter depends on whether native BLVRB is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
BLVRB is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label BLVRB as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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