SPIN4
Spindlin-4
Also known as: FLJ44984, SPIN4_HUMAN, TDRD28
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q56A73
- Gene
- SPIN4
- Ensembl
- ENSG00000186767
- Chromosome
- X
- Canonical length
- 249 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Centrosome,Cytosol
OverviewNCBI Gene
Enables methylated histone binding activity. Involved in negative regulation of cell population proliferation and positive regulation of canonical Wnt signaling pathway. Located in chromatin; cytoplasm; and nucleus. [provided by Alliance of Genome Resources, Apr 2025]
Canonical amino-acid sequenceUniProt
249 residues, UniProt reviewed canonical sequence.
>Q56A73|SPIN4
1 MSPPTVPPMG VDGVSAYLMK KRHTHRKQRR KPTFLTRRNI VGCRIQHGWK EGNEPVEQWK
61 GTVLEQVSVK PTLYIIKYDG KDSVYGLELH RDKRVLALEI LPERVPTPRI DSRLADSLIG
121 KAVEHVFEGE HGTKDEWKGM VLARAPVMDT WFYITYEKDP VLYMYTLLDD YKDGDLRIIP
181 DSNYYFPTAE QEPGEVVDSL VGKQVEHAKD DGSKRTGIFI HQVVAKPSVY FIKFDDDIHI
241 YVYGLVKTPLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SPIN4 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)
- 0.37
- Highest tissue expression
- 9.6 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 9.6 nTPM
- salivary gland: 6.8 nTPM
- esophagus: 5.5 nTPM
- tonsil: 5.2 nTPM
- placenta: 4.1 nTPM
- rectum: 3.8 nTPM
Single-cell type
- podocytes: 5.9 nCPM
- proximal tubule cells: 3 nCPM
- loop of henle epithelial cells: 2.3 nCPM
- distal convoluted tubule cells: 2.2 nCPM
- renal connecting tubule cells: 2.1 nCPM
- renal collecting duct intercalated cells: 1.5 nCPM
Immune cell
- NK-cell: 2.6 nTPM
- eosinophil: 1.6 nTPM
- intermediate monocyte: 0.9 nTPM
- classical monocyte: 0.8 nTPM
- non-classical monocyte: 0.8 nTPM
- basophil: 0.7 nTPM
Brain region
- hypothalamus: 8.7 nTPM
- midbrain: 6.4 nTPM
- choroid plexus: 5.6 nTPM
- medulla oblongata: 5.6 nTPM
- white matter: 5.5 nTPM
- pons: 5.4 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about SPIN4.
Disease | AllUniProt
Conditions SPIN4 is implicated in, by any mechanism.
- Lui-Jee-Baron syndrome (LJBS) MIM:301114
Disease | GeneticClinVar
1 pathogenic / likely-pathogenic of 15 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Lui-Jee-Baron syndrome
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)
- 0.64
- gnomAD pLI
- 0.76
- gnomAD missense Z
- 1.58
- DepMap mean gene effect
- 0.14
- DepMap dependency class
- none
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
- gamete generation
- negative regulation of cell population proliferation
- positive regulation of canonical Wnt signaling pathway
- regulation of DNA-templated transcription
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SPIN4 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 SPIN4 as an antibody target. Whether an autoantibody or antibody against SPIN4 could matter depends on whether native SPIN4 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SPIN4 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 SPIN4 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
Loading the interactive Seroatlas protein explorer...