ALYREF
THO complex subunit 4
Also known as: THOC4_HUMAN
Protein identityUniProt · HPA
- UniProt accession
- Q86V81
- Gene
- ALYREF
- Canonical length
- 257 aa
- Protein class
- Predicted intracellular proteins
- Quaternary structure
- Homomultimer
OverviewNCBI Gene
No narrative summary is available for ALYREF in this catalog release; identity and structured annotations are shown without generated factual claims.
Canonical amino-acid sequenceUniProt
257 residues, UniProt reviewed canonical sequence.
>Q86V81|ALYREF
1 MADKMDMSLD DIIKLNRSQR GGRGGGRGRG RAGSQGGRGG GAQAAARVNR GGGPIRNRPA
61 IARGAAGGGG RNRPAPYSRP KQLPDKWQHD LFDSGFGGGA GVETGGKLLV SNLDFGVSDA
121 DIQELFAEFG TLKKAAVHYD RSGRSLGTAD VHFERKADAL KAMKQYNGVP LDGRPMNIQL
181 VTSQIDAQRR PAQSVNRGGM TRNRGAGGFG GGGGTRRGTR GGARGRGRGA GRNSKQQLSA
241 EELDAQLDAY NARMDTSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ALYREF 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)
- 0.58
- Highest tissue expression
- 141 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 141 nTPM
- testis: 68 nTPM
- thymus: 61 nTPM
- lymph node: 58 nTPM
- skeletal muscle: 58 nTPM
- esophagus: 55 nTPM
Single-cell type
- erythrocyte progenitors: 160 nCPM
- megakaryocytes: 99 nCPM
- monocyte progenitors: 94 nCPM
- megakaryocyte progenitors: 90 nCPM
- gastric progenitor cells: 72 nCPM
- pdcs: 59 nCPM
Immune cell
- plasmacytoid DC: 2.2 nTPM
- gdT-cell: 1.5 nTPM
- intermediate monocyte: 1.2 nTPM
- myeloid DC: 1.2 nTPM
- naive B-cell: 1.2 nTPM
- classical monocyte: 1.1 nTPM
Brain region
- white matter: 33 nTPM
- spinal cord: 31 nTPM
- pons: 31 nTPM
- cerebral cortex: 31 nTPM
- midbrain: 30 nTPM
- thalamus: 29 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about ALYREF.
Disease | ImmuneIEDB
Conditions an epitope on ALYREF was assayed in.
- skin melanoma T cell
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)
- 0.36
- gnomAD pLI
- 0.93
- gnomAD missense Z
- 2.31
- DepMap mean gene effect
- -1.34
- DepMap dependency class
- pan
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 8% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- mRNA export from nucleus
- mRNA processing
- osteoblast differentiation
- RNA export from nucleus
- RNA splicing
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of ALYREF 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 ALYREF as an antibody target. Whether an autoantibody or antibody against ALYREF could matter depends on whether native ALYREF is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ALYREF 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 ALYREF as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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