SPIRE2
Protein spire homolog 2
Also known as: KIAA1832, spir-2, SPIR2_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8WWL2
- Gene
- SPIRE2
- Ensembl
- ENSG00000204991
- Chromosome
- 16
- Canonical length
- 714 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Vesicles,Intermediate filaments
OverviewNCBI Gene
Predicted to enable microtubule binding activity. Involved in establishment of meiotic spindle localization; formin-nucleated actin cable assembly; and positive regulation of double-strand break repair. Predicted to be located in cleavage furrow. Predicted to be active in cell cortex and cytoplasmic vesicle membrane. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
714 residues, UniProt reviewed canonical sequence.
>Q8WWL2|SPIRE2
1 MARAGSCGGA AAGAGRPEPW ELSLEEVLKA YEQPLNEEQA WAVCFQGCRG LRGSPGRRLR
61 DTGDLLLRGD GSVGAREPEA AEPATMVVPL ASSEAQTVQS LGFAIYRALD WGLDESEERE
121 LSPQLERLID LMANNDSEDS GCGAADEGYG GPEEEEEAEG VPRSVRTFAQ AMRLCAARLT
181 DPRGAQAHYQ AVCRALFVET LELRAFLARV REAKEMLQKL REDEPHLETP RAELDSLGHT
241 DWARLWVQLM RELRRGVKLK KVQEQEFNPL PTEFQLTPFE MLMQDIRARN YKLRKVMVDG
301 DIPPRVKKDA HELILDFIRS RPPLKQVSER RLRPLPPKQR SLHEKILEEI KQERRLRPVR
361 GEGWAARGFG SLPCILNACS GDAKSTSCIN LSVTDAGGSA QRPRPRVLLK APTLAEMEEM
421 NTSEEEESPC GEVTLKRDRS FSEHDLAQLR SEVASGLQSA THPPGGTEPP RPRAGSAHVW
481 RPGSRDQGTC PASVSDPSHP LLSNRGSSGD RPEASMTPDA KHLWLEFSHP VESLALTVEE
541 VMDVRRVLVK AEMEKFLQNK ELFSSLKKGK ICCCCRAKFP LFSWPPSCLF CKRAVCTSCS
601 IKMKMPSKKF GHIPVYTLGF ESPQRVSAAK TAPIQRRDIF QSLQGPQWQS VEEAFPHIYS
661 HGCVLKDVCS ECTSFVADVV RSSRKSVDVL NTTPRRSRQT QSLYIPNTRT LDFKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SPIRE2 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
- Cell surface
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.49
- Highest tissue expression
- 25 nTPM
Expression across tissuesHPA
Tissue
- cerebellum: 25 nTPM
- pituitary gland: 21 nTPM
- colon: 15 nTPM
- cerebral cortex: 15 nTPM
- stomach: 14 nTPM
- basal ganglia: 12 nTPM
Single-cell type
- somatotrophs: 214 nCPM
- syncytiotrophoblasts: 148 nCPM
- foveolar cells: 142 nCPM
- prostatic club cells: 141 nCPM
- prostatic hillock cells: 132 nCPM
- urothelial cells: 132 nCPM
Immune cell
- basophil: 2.3 nTPM
- neutrophil: 1.9 nTPM
- naive B-cell: 0.7 nTPM
- NK-cell: 0.6 nTPM
- classical monocyte: 0.5 nTPM
- memory B-cell: 0.5 nTPM
Brain region
- cerebral cortex: 30 nTPM
- cerebellum: 29 nTPM
- pons: 26 nTPM
- medulla oblongata: 23 nTPM
- basal ganglia: 23 nTPM
- midbrain: 22 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)
- 0.86
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.26
- DepMap mean gene effect
- 0.05
- 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
- actin cytoskeleton organization
- actin filament network formation
- actin nucleation
- cleavage furrow formation
- establishment of meiotic spindle localization
- formin-nucleated actin cable assembly
- Golgi vesicle transport
- intracellular transport
- polar body extrusion after meiotic divisions
- positive regulation of double-strand break repair
- protein transport
- vesicle-mediated transport
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads SPIRE2 as an antibody target. Whether an autoantibody or antibody against SPIRE2 could matter depends on whether native SPIRE2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SPIRE2 is annotated at the cell surface, where native SPIRE2 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label SPIRE2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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