UBL7
Ubiquitin-like protein 7
Also known as: BMSC-UbP, MGC14421, UBL7_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96S82
- Gene
- UBL7
- Ensembl
- ENSG00000138629
- Chromosome
- 15
- Canonical length
- 380 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Cytosol
OverviewNCBI Gene
Enables protein-macromolecule adaptor activity. Involved in antiviral innate immune response. Is active in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
380 residues, UniProt reviewed canonical sequence.
>Q96S82|UBL7
1 MSLSDWHLAV KLADQPLTPK SILRLPETEL GEYSLGGYSI SFLKQLIAGK LQESVPDPEL
61 IDLIYCGRKL KDDQTLDFYG IQPGSTVHVL RKSWPEPDQK PEPVDKVAAM REFRVLHTAL
121 HSSSSYREAV FKMLSNKESL DQIIVATPGL SSDPIALGVL QDKDLFSVFA DPNMLDTLVP
181 AHPALVNAIV LVLHSVAGSA PMPGTDSSSR SMPSSSYRDM PGGFLFEGLS DDEDDFHPNT
241 RSTPSSSTPS SRPASLGYSG AAGPRPITQS ELATALALAS TPESSSHTPT PGTQGHSSGT
301 SPMSSGVQSG TPITNDLFSQ ALQHALQASG QPSLQSQWQP QLQQLRDMGI QDDELSLRAL
361 QATGGDIQAA LELIFAGGAPLocalizationUniProt · AlphaFold · HPA
Whether an antibody against UBL7 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)
- 0.46
- Highest tissue expression
- 110 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 110 nTPM
- cerebral cortex: 80 nTPM
- heart muscle: 65 nTPM
- spinal cord: 65 nTPM
- amygdala: 63 nTPM
- hippocampal formation: 61 nTPM
Single-cell type
- late spermatids: 248 nCPM
- late primary spermatocytes: 81 nCPM
- early spermatids: 56 nCPM
- extravillous trophoblasts: 50 nCPM
- cytotrophoblasts: 48 nCPM
- migrating cytotrophoblasts: 46 nCPM
Immune cell
- plasmacytoid DC: 152 nTPM
- myeloid DC: 71 nTPM
- T-reg: 66 nTPM
- neutrophil: 66 nTPM
- eosinophil: 60 nTPM
- intermediate monocyte: 59 nTPM
Brain region
- cerebral cortex: 31 nTPM
- pons: 30 nTPM
- basal ganglia: 29 nTPM
- white matter: 29 nTPM
- midbrain: 27 nTPM
- hippocampal formation: 26 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)
- 0.77
- gnomAD pLI
- 0
- gnomAD missense Z
- 1.29
- DepMap mean gene effect
- -0.05
- 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
- Ubiquitin-like domain
- UBA-like superfamily
- Ubiquilin
- Ubiquitin-associated domain
- Ubiquitin-like domain superfamily
- Ubiquitin family
- Ubiquitin-like protein 7, ubiquitin-like domain
- Ubiquitin-like protein 7, UBA domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of UBL7 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 UBL7 as an antibody target. Whether an autoantibody or antibody against UBL7 could matter depends on whether native UBL7 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
UBL7 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 UBL7 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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