SPEF1
Sperm flagellar protein 1
Also known as: C20orf28, CLAMP, DKFZP434I114, SPEF1_HUMAN, SPEF1A
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9Y4P9
- Gene
- SPEF1
- Ensembl
- ENSG00000101222
- Chromosome
- 20
- Canonical length
- 236 aa
- Protein class
- Predicted intracellular proteins
- Quaternary structure
- Homodimer
OverviewNCBI Gene
Enables actin binding activity. Involved in filopodium assembly and lamellipodium assembly. Located in several cellular components, including basolateral plasma membrane; lamellipodium; and microvillus. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
236 residues, UniProt reviewed canonical sequence.
>Q9Y4P9|SPEF1
1 MASSVDEEAL HQLYLWVDNI PLSRPKRNLS RDFSDGVLVA EVIKFYFPKM VEMHNYVPAN
61 SLQQKLSNWG HLNRKVLKRL NFSVPDDVMR KIAQCAPGVV ELVLIPLRQR LEERQRRRKQ
121 GAGSLQELAP QDGSGYMDVG VSQKARGEGV PDPQGGGQLS WDRPPAPRPP AYNRALQGDP
181 SFVLQIAEKE QELLASQETV QVLQMKVRRL EHLLQLKNVR IEDLSRRLQQ AERKQRLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SPEF1 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)
- 0.45
- Highest tissue expression
- 28 nTPM
Expression across tissuesHPA
Tissue
- basal ganglia: 28 nTPM
- choroid plexus: 24 nTPM
- hippocampal formation: 14 nTPM
- testis: 12 nTPM
- fallopian tube: 9.3 nTPM
- cerebral cortex: 8.2 nTPM
Single-cell type
- epididymal efferent duct ciliated cells: 214 nCPM
- respiratory ciliated cells: 166 nCPM
- fallopian tube ciliated cells: 165 nCPM
- endometrial ciliated cells: 118 nCPM
- ependymal cells: 87 nCPM
- brain inhibitory neurons: 37 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- choroid plexus: 31 nTPM
- basal ganglia: 17 nTPM
- midbrain: 16 nTPM
- medulla oblongata: 14 nTPM
- spinal cord: 12 nTPM
- hippocampal formation: 8.7 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)
- 1.23
- gnomAD pLI
- 0
- gnomAD missense Z
- 1.17
- DepMap mean gene effect
- -0.15
- 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
- axonemal central apparatus assembly
- cell migration
- cilium movement
- filopodium assembly
- lamellipodium assembly
- microtubule bundle formation
- negative regulation of microtubule depolymerization
- regulation of cytoskeleton organization
- regulation of Wnt signaling pathway, planar cell polarity pathway
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SPEF1 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 SPEF1 as an antibody target. Whether an autoantibody or antibody against SPEF1 could matter depends on whether native SPEF1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SPEF1 is annotated at the cell surface, where native SPEF1 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 SPEF1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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