FRRS1
Ferric-chelate reductase 1
Also known as: FRRS1_HUMAN, SDFR2, SDR2
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q6ZNA5
- Gene
- FRRS1
- Ensembl
- ENSG00000156869
- Chromosome
- 1
- Canonical length
- 592 aa
- Protein class
- Predicted membrane proteins
OverviewNCBI Gene
Members of the cytochrome b561 (CYB561; MIM 600019) family, including FRRS1, reduce ferric to ferrous iron before its transport from the endosome to the cytoplasm (Vargas et al., 2003 [PubMed 14499595]).[supplied by OMIM, Mar 2008]
Canonical amino-acid sequenceUniProt
592 residues, UniProt reviewed canonical sequence.
>Q6ZNA5|FRRS1
1 MAVSGFTLGT CILLLHISYV ANYPNGKVTQ SCHGMIPEHG HSPQSVPVHD IYVSQMTFRP
61 GDQIEVTLSG HPFKGFLLEA RNAEDLNGPP IGSFTLIDSE VSQLLTCEDI QGSAVSHRSA
121 SKKTEIKVYW NAPSSAPNHT QFLVTVVEKY KIYWVKIPGP IISQPNAFPF TTPKATVVPL
181 PTLPPVSHLT KPFSASDCGN KKFCIRSPLN CDPEKEASCV FLSFTRDDQS VMVEMSGPSK
241 GYLSFALSHD QWMGDDDAYL CIHEDQTVYI QPSHLTGRSH PVMDSRDTLE DMAWRLADGV
301 MQCSFRRNIT LPGVKNRFDL NTSYYIFLAD GAANDGRIYK HSQQPLITYE KYDVTDSPKN
361 IGGSHSVLLL KVHGALMFVA WMTTVSIGVL VARFFKPVWS KAFLLGEAAW FQVHRMLMFT
421 TTVLTCIAFV MPFIYRGGWS RHAGYHPYLG CIVMTLAVLQ PLLAVFRPPL HDPRRQMFNW
481 THWSMGTAAR IIAVAAMFLG MDLPGLNLPD SWKTYAMTGF VAWHVGTEVV LEVHAYRLSR
541 KVEILDDDRI QILQSFTAVE TEGHAFKKAV LAIYVCGNVT FLIIFLSAIN HLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against FRRS1 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
- Unknown
- Secreted
- No
- Transmembrane segments
- 7
- Mean surface accessibility (rSASA)
- 0.29
- Highest tissue expression
- 27 nTPM
Expression across tissuesHPA
Tissue
- liver: 27 nTPM
- placenta: 9.5 nTPM
- skin: 8.7 nTPM
- epididymis: 6.9 nTPM
- esophagus: 6.9 nTPM
- vagina: 5 nTPM
Single-cell type
- hepatocytes: 110 nCPM
- esophageal apical cells: 101 nCPM
- syncytiotrophoblasts: 78 nCPM
- esophageal suprabasal cells: 59 nCPM
- basal keratinocytes: 58 nCPM
- suprabasal keratinocytes: 58 nCPM
Immune cell
- eosinophil: 12 nTPM
- intermediate monocyte: 1.4 nTPM
- myeloid DC: 1.3 nTPM
- basophil: 1.2 nTPM
- classical monocyte: 1 nTPM
- plasmacytoid DC: 0.9 nTPM
Brain region
- choroid plexus: 11 nTPM
- white matter: 10 nTPM
- medulla oblongata: 9.2 nTPM
- cerebral cortex: 8.9 nTPM
- thalamus: 8.9 nTPM
- pons: 8.7 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)
- 0.85
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.57
- DepMap mean gene effect
- -0.07
- 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
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads FRRS1 as an antibody target. Whether an autoantibody or antibody against FRRS1 could matter depends on whether native FRRS1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
FRRS1 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 FRRS1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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