SPDYA
Speedy protein A
Also known as: Ringo3, SPDY1, SPDYA_HUMAN, SPY1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q5MJ70
- Gene
- SPDYA
- Ensembl
- ENSG00000163806
- Chromosome
- 2
- Canonical length
- 313 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
Enables protein kinase activator activity and protein kinase binding activity. Involved in several processes, including G1/S transition of mitotic cell cycle; positive regulation of cell population proliferation; and positive regulation of protein kinase activity. Located in nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
313 residues, UniProt reviewed canonical sequence.
>Q5MJ70|SPDYA
1 MRHNQMCCET PPTVTVYVKS GSNRSHQPKK PITLKRPICK DNWQAFEKNT HNNNKSKRPK
61 GPCLVIQRQD MTAFFKLFDD DLIQDFLWMD CCCKIADKYL LAMTFVYFKR AKFTISEHTR
121 INFFIALYLA NTVEEDEEET KYEIFPWALG KNWRKLFPNF LKLRDQLWDR IDYRAIVSRR
181 CCEEVMAIAP THYIWQRERS VHHSGAVRNY NRDEVQLPRG PSATPVDCSL CGKKRRYVRL
241 GLSSSSSLSS HTAGVTEKHS QDSYNSLSMD IIGDPSQAYT GSEVVNDHQS NKGKKTNFLK
301 KDKSMEWFTG SEELocalizationUniProt · AlphaFold · HPA
Whether an antibody against SPDYA 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)
- 0.47
- Highest tissue expression
- 31 nTPM
Expression across tissuesHPA
Tissue
- testis: 31 nTPM
- cerebellum: 2.3 nTPM
- spleen: 1.7 nTPM
- prostate: 1.6 nTPM
- skin: 1.5 nTPM
- liver: 1.4 nTPM
Single-cell type
- early primary spermatocytes: 497 nCPM
- neutrophils: 357 nCPM
- late primary spermatocytes: 337 nCPM
- endometrial luminal cells: 210 nCPM
- endometrial ciliated cells: 134 nCPM
- endometrial glandular cells: 128 nCPM
Immune cell
- gdT-cell: 0.1 nTPM
- plasmacytoid DC: 0.1 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- intermediate monocyte: 0 nTPM
Brain region
- cerebral cortex: 2.7 nTPM
- hippocampal formation: 2.7 nTPM
- cerebellum: 2.6 nTPM
- amygdala: 2.5 nTPM
- basal ganglia: 2.3 nTPM
- hypothalamus: 2.3 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)
- 0.51
- gnomAD pLI
- 0.55
- gnomAD missense Z
- 1.56
- 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
- DNA damage response
- establishment of protein localization to telomere
- G1/S transition of mitotic cell cycle
- male meiotic nuclear division
- meiotic attachment of telomere to nuclear envelope
- oogenesis
- positive regulation of cell population proliferation
- spermatogenesis
- telomere capping
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SPDYA 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 SPDYA as an antibody target. Whether an autoantibody or antibody against SPDYA could matter depends on whether native SPDYA is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SPDYA 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 SPDYA as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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