SPIN1
Spindlin-1
Also known as: SPIN, SPIN1_HUMAN, TDRD24
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9Y657
- Gene
- SPIN1
- Ensembl
- ENSG00000106723
- Chromosome
- 9
- Canonical length
- 262 aa
- Protein class
- Plasma proteins, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm
- Quaternary structure
- Homodimer
OverviewNCBI Gene
Enables histone reader activity and methylated histone binding activity. Involved in positive regulation of DNA-templated transcription; positive regulation of Wnt signaling pathway; and rRNA transcription. Located in cytosol and nucleus. [provided by Alliance of Genome Resources, Apr 2025]
Canonical amino-acid sequenceUniProt
262 residues, UniProt reviewed canonical sequence.
>Q9Y657|SPIN1
1 MKTPFGKTPG QRSRADAGHA GVSANMMKKR TSHKKHRSSV GPSKPVSQPR RNIVGCRIQH
61 GWKEGNGPVT QWKGTVLDQV PVNPSLYLIK YDGFDCVYGL ELNKDERVSA LEVLPDRVAT
121 SRISDAHLAD TMIGKAVEHM FETEDGSKDE WRGMVLARAP VMNTWFYITY EKDPVLYMYQ
181 LLDDYKEGDL RIMPDSNDSP PAEREPGEVV DSLVGKQVEY AKEDGSKRTG MVIHQVEAKP
241 SVYFIKFDDD FHIYVYDLVK TSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SPIN1 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)
- 0.4
- Highest tissue expression
- 73 nTPM
Expression across tissuesHPA
Tissue
- epididymis: 73 nTPM
- endometrium: 57 nTPM
- cervix: 56 nTPM
- cerebral cortex: 52 nTPM
- ovary: 50 nTPM
- fallopian tube: 48 nTPM
Single-cell type
- choroid plexus epithelial cells: 422 nCPM
- sertoli cells: 413 nCPM
- ependymal cells: 332 nCPM
- pituitary stem cells: 311 nCPM
- distal convoluted tubule cells: 305 nCPM
- renal connecting tubule cells: 264 nCPM
Immune cell
- basophil: 7.4 nTPM
- myeloid DC: 5 nTPM
- naive CD8 T-cell: 4.5 nTPM
- eosinophil: 4.2 nTPM
- MAIT T-cell: 4.1 nTPM
- memory CD8 T-cell: 4 nTPM
Brain region
- cerebral cortex: 84 nTPM
- basal ganglia: 82 nTPM
- hypothalamus: 82 nTPM
- midbrain: 73 nTPM
- white matter: 71 nTPM
- hippocampal formation: 66 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)
- 0.27
- gnomAD pLI
- 0.97
- gnomAD missense Z
- 3.25
- DepMap mean gene effect
- -0.02
- 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
- gamete generation
- meiotic cell cycle
- positive regulation of DNA-templated transcription
- positive regulation of Wnt signaling pathway
- protein localization to chromatin
- regulation of DNA-templated transcription
- rRNA transcription
- transposable element silencing by piRNA-mediated DNA methylation
- Wnt signaling pathway
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SPIN1 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 SPIN1 as an antibody target. Whether an autoantibody or antibody against SPIN1 could matter depends on whether native SPIN1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SPIN1 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 SPIN1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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