UBL4A
Ubiquitin-like protein 4A
Also known as: DXS254E, GDX, GET5, MDY2, TMA24, UBL4, UBL4A_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P11441
- Gene
- UBL4A
- Ensembl
- ENSG00000102178
- Chromosome
- X
- Canonical length
- 157 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Cytosol
OverviewNCBI Gene
Enables protein-folding chaperone binding activity. Involved in establishment of protein localization to membrane; regulation of protein stability; and ubiquitin-dependent protein catabolic process. Located in cytosol; membrane; and nucleoplasm. Part of BAT3 complex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
157 residues, UniProt reviewed canonical sequence.
>P11441|UBL4A
1 MQLTVKALQG RECSLQVPED ELVSTLKQLV SEKLNVPVRQ QRLLFKGKAL ADGKRLSDYS
61 IGPNSKLNLV VKPLEKVLLE EGEAQRLADS PPPQVWQLIS KVLARHFSAA DASRVLEQLQ
121 RDYERSLSRL TLDDIERLAS RFLHPEVTET MEKGFSKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against UBL4A 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)
- 0.42
- Highest tissue expression
- 92 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 92 nTPM
- tongue: 68 nTPM
- heart muscle: 46 nTPM
- cerebral cortex: 40 nTPM
- pancreas: 36 nTPM
- adrenal gland: 29 nTPM
Single-cell type
- platelets: 436 nCPM
- megakaryocytes: 210 nCPM
- esophageal basal cells: 56 nCPM
- esophageal suprabasal cells: 53 nCPM
- extravillous trophoblasts: 52 nCPM
- migrating cytotrophoblasts: 51 nCPM
Immune cell
- basophil: 95 nTPM
- MAIT T-cell: 47 nTPM
- total PBMC: 42 nTPM
- memory CD8 T-cell: 36 nTPM
- NK-cell: 34 nTPM
- T-reg: 34 nTPM
Brain region
- cerebral cortex: 42 nTPM
- white matter: 32 nTPM
- thalamus: 29 nTPM
- hippocampal formation: 29 nTPM
- pons: 28 nTPM
- basal ganglia: 28 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)
- 1.18
- gnomAD pLI
- 0.3
- gnomAD missense Z
- 0.7
- DepMap mean gene effect
- -0.08
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 7% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- post-translational protein targeting to endoplasmic reticulum membrane
- protein modification process
- regulation of protein stability
- tail-anchored membrane protein insertion into ER membrane
- ubiquitin-dependent protein catabolic process
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Ubiquitin-like domain
- Ubiquitin conserved site
- Ubiquitin domain
- Ubiquitin-like domain superfamily
- Ubl4, C-terminal TUGS domain
- Ubiquitin family
- Tethering Ubl4a to BAGS domain
- UBL4A-like, ubiquitin-like domain
- Ubiquitin-like protein 4A-like
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of UBL4A 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 UBL4A as an antibody target. Whether an autoantibody or antibody against UBL4A could matter depends on whether native UBL4A is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
UBL4A 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 UBL4A as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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