FXR2
RNA-binding protein FXR2
Also known as: FMR1L2, FXR2_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P51116
- Gene
- FXR2
- Ensembl
- ENSG00000129245
- Chromosome
- 17
- Canonical length
- 673 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Cytosol
OverviewNCBI Gene
The protein encoded by this gene is a RNA binding protein containing two KH domains and one RCG box, which is similar to FMRP and FXR1. It associates with polyribosomes, predominantly with 60S large ribosomal subunits. This encoded protein may self-associate or interact with FMRP and FXR1. It may have a role in the development of fragile X cognitive disability syndrome. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
673 residues, UniProt reviewed canonical sequence.
>P51116|FXR2
1 MGGLASGGDV EPGLPVEVRG SNGAFYKGFV KDVHEDSVTI FFENNWQSER QIPFGDVRLP
61 PPADYNKEIT EGDEVEVYSR ANEQEPCGWW LARVRMMKGD FYVIEYAACD ATYNEIVTLE
121 RLRPVNPNPL ATKGSFFKVT MAVPEDLREA CSNENVHKEF KKALGANCIF LNITNSELFI
181 LSTTEAPVKR ASLLGDMHFR SLRTKLLLMS RNEEATKHLE TSKQLAAAFQ EEFTVREDLM
241 GLAIGTHGAN IQQARKVPGV TAIELGEETC TFRIYGETPE ACRQARSYLE FSEDSVQVPR
301 NLVGKVIGKN GKVIQEIVDK SGVVRVRVEG DNDKKNPREE GMVPFIFVGT RENISNAQAL
361 LEYHLSYLQE VEQLRLERLQ IDEQLRQIGL GFRPPGSGRG SGGSDKAGYS TDESSSSSLH
421 ATRTYGGSYG GRGRGRRTGG PAYGPSSDVS TASETESEKR EEPNRAGPGD RDPPTRGEES
481 RRRPTGGRGR GPPPAPRPTS RYNSSSISSV LKDPDSNPYS LLDTSEPEPP VDSEPGEPPP
541 ASARRRRSRR RRTDEDRTVM DGGLESDGPN MTENGLEDES RPQRRNRSRR RRNRGNRTDG
601 SISGDRQPVT VADYISRAES QSRQRPPLER TKPSEDSLSG QKGDSVSKLP KGPSENGELS
661 APLELGSMVN GVSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against FXR2 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)
- 0.49
- Highest tissue expression
- 113 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 113 nTPM
- tongue: 79 nTPM
- heart muscle: 61 nTPM
- cerebellum: 46 nTPM
- cerebral cortex: 41 nTPM
- midbrain: 39 nTPM
Single-cell type
- thymic myoid cells: 56 nCPM
- retinal pigment epithelial cells: 43 nCPM
- cardiomyocytes: 41 nCPM
- retinal horizontal cells: 38 nCPM
- early primary spermatocytes: 37 nCPM
- rod photoreceptor cells: 33 nCPM
Immune cell
- basophil: 2.6 nTPM
- eosinophil: 2.5 nTPM
- neutrophil: 2.1 nTPM
- memory CD8 T-cell: 1.9 nTPM
- T-reg: 1.8 nTPM
- memory CD4 T-cell: 1.5 nTPM
Brain region
- pons: 76 nTPM
- midbrain: 71 nTPM
- medulla oblongata: 70 nTPM
- hypothalamus: 68 nTPM
- cerebral cortex: 62 nTPM
- thalamus: 61 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)
- 0.19
- gnomAD pLI
- 1
- gnomAD missense Z
- 2.62
- DepMap mean gene effect
- -0.06
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- animal organ development
- dentate gyrus development
- mRNA destabilization
- mRNA transport
- positive regulation of long-term neuronal synaptic plasticity
- positive regulation of translation
- regulation of mRNA stability
- regulation of translation at presynapse, modulating synaptic transmission
Molecular functions
- identical protein binding
- mRNA 3'-UTR binding
- protein heterodimerization activity
- protein homodimerization activity
- RNA binding
- translation regulator activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
- K Homology domain
- K Homology domain, type 1
- Agenet-like domain
- Fragile X messenger ribonucleoprotein 1-like, C-terminal core
- Fragile X-related protein 1, C-terminal region 1
- K Homology domain, type 1 superfamily
- Fragile X messenger ribonucleoprotein 1
- Synaptic functional regulator FMRP, KH0 domain
- FMR1, tudor domain
- KH domain
- Agenet domain
- Fragile X-related 1 protein core C terminal
- Fragile X-related 1 protein C-terminal region 2
- FMRP KH0 domain
- Fragile X messenger ribonucleoprotein 1, Tudor domain
- RNA-binding protein FXR2, second Tudor-like Agenet domain
- RNA-binding protein FXR2, first Tudor-like Agenet domain
- RNA-binding protein FXR2, first type I K homology domain
- RNA-binding protein FXR2, second type I K homology domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of FXR2 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads FXR2 as an antibody target. Whether an autoantibody or antibody against FXR2 could matter depends on whether native FXR2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
FXR2 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 FXR2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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