CYBRD1
Plasma membrane ascorbate-dependent reductase CYBRD1
Also known as: CYB561A2, CYBR1_HUMAN, DCYTB, FLJ23462, FRRS3
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q53TN4
- Gene
- CYBRD1
- Ensembl
- ENSG00000071967
- Chromosome
- 2
- Canonical length
- 286 aa
- Protein class
- Enzymes, Metabolic proteins, Predicted membrane proteins, Transporters
- Subcellular location
- Plasma membrane
- Quaternary structure
- Homodimer
OverviewNCBI Gene
This gene is a member of the cytochrome b(561) family that encodes an iron-regulated protein. It highly expressed in the duodenal brush border membrane. It has ferric reductase activity and is believed to play a physiological role in dietary iron absorption. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
286 residues, UniProt reviewed canonical sequence.
>Q53TN4|CYBRD1
1 MAMEGYWRFL ALLGSALLVG FLSVIFALVW VLHYREGLGW DGSALEFNWH PVLMVTGFVF
61 IQGIAIIVYR LPWTWKCSKL LMKSIHAGLN AVAAILAIIS VVAVFENHNV NNIANMYSLH
121 SWVGLIAVIC YLLQLLSGFS VFLLPWAPLS LRAFLMPIHV YSGIVIFGTV IATALMGLTE
181 KLIFSLRDPA YSTFPPEGVF VNTLGLLILV FGALIFWIVT RPQWKRPKEP NSTILHPNGG
241 TEQGARGSMP AYSGNNMDKS DSELNSEVAA RKRNLALDEA GQRSTMLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CYBRD1 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
- Cell surface
- Secreted
- No
- Transmembrane segments
- 6
- Mean surface accessibility (rSASA)
- 0.34
- Highest tissue expression
- 220 nTPM
Expression across tissuesHPA
Tissue
- small intestine: 220 nTPM
- thyroid gland: 217 nTPM
- duodenum: 186 nTPM
- blood vessel: 183 nTPM
- adipose tissue: 164 nTPM
- ovary: 162 nTPM
Single-cell type
- enterocytes: 873 nCPM
- fibroblasts: 337 nCPM
- peritubular myoid cells: 264 nCPM
- leydig cells: 252 nCPM
- fibro-adipogenic progenitors: 164 nCPM
- alveolar cells type 1: 158 nCPM
Immune cell
- intermediate monocyte: 18 nTPM
- classical monocyte: 17 nTPM
- myeloid DC: 17 nTPM
- non-classical monocyte: 14 nTPM
- neutrophil: 9.8 nTPM
- total PBMC: 7.5 nTPM
Brain region
- hypothalamus: 81 nTPM
- medulla oblongata: 80 nTPM
- white matter: 71 nTPM
- midbrain: 66 nTPM
- basal ganglia: 64 nTPM
- thalamus: 60 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)
- 0.89
- gnomAD pLI
- 0.01
- gnomAD missense Z
- 0.59
- DepMap mean gene effect
- -0.04
- 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
- ascorbate homeostasis
- intracellular iron ion homeostasis
- multicellular organismal-level iron ion homeostasis
- response to iron ion
- reductive iron assimilation
Molecular functions
- identical protein binding
- metal ion binding
- oxidoreductase activity
- oxidoreductase activity, acting on metal ions
- transmembrane ascorbate ferrireductase activity
- transmembrane monodehydroascorbate reductase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads CYBRD1 as an antibody target. Whether an autoantibody or antibody against CYBRD1 could matter depends on whether native CYBRD1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CYBRD1 is annotated at the cell surface, where native CYBRD1 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label CYBRD1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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