NEK10
Serine/threonine-protein kinase Nek10
Also known as: FLJ32685, NEK10_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q6ZWH5
- Gene
- NEK10
- Ensembl
- ENSG00000163491
- Chromosome
- 3
- Canonical length
- 1172 aa
- Protein class
- Disease related genes, Enzymes, Human disease related genes, Potential drug targets, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Vesicles
OverviewNCBI Gene
Enables protein kinase activity. Involved in several processes, including mucociliary clearance; positive regulation of protein phosphorylation; and regulation of ERK1 and ERK2 cascade. Part of protein kinase complex. Implicated in primary ciliary dyskinesia 44. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
1172 residues, UniProt reviewed canonical sequence.
>Q6ZWH5|NEK10
1 MPDQDKKVKT TEKSTDKQQE ITIRDYSDLK RLRCLLNVQS SKQQLPAINF DSAQNSMTKS
61 EPAIRAGGHR ARGQWHESTE AVELENFSIN YKNERNFSKH PQRKLFQEIF TALVKNRLIS
121 REWVNRAPSI HFLRVLICLR LLMRDPCYQE ILHSLGGIEN LAQYMEIVAN EYLGYGEEQH
181 TVDKLVNMTY IFQKLAAVKD QREWVTTSGA HKTLVNLLGA RDTNVLLGSL LALASLAESQ
241 ECREKISELN IVENLLMILH EYDLLSKRLT AELLRLLCAE PQVKEQVKLY EGIPVLLSLL
301 HSDHLKLLWS IVWILVQVCE DPETSVEIRI WGGIKQLLHI LQGDRNFVSD HSSIGSLSSA
361 NAAGRIQQLH LSEDLSPREI QENTFSLQAA CCAALTELVL NDTNAHQVVQ ENGVYTIAKL
421 ILPNKQKNAA KSNLLQCYAF RALRFLFSME RNRPLFKRLF PTDLFEIFID IGHYVRDISA
481 YEELVSKLNL LVEDELKQIA ENIESINQNK APLKYIGNYA ILDHLGSGAF GCVYKVRKHS
541 GQNLLAMKEV NLHNPAFGKD KKDRDSSVRN IVSELTIIKE QLYHPNIVRY YKTFLENDRL
601 YIVMELIEGA PLGEHFSSLK EKHHHFTEER LWKIFIQLCL ALRYLHKEKR IVHRDLTPNN
661 IMLGDKDKVT VTDFGLAKQK QENSKLTSVV GTILYSCPEV LKSEPYGEKA DVWAVGCILY
721 QMATLSPPFY STNMLSLATK IVEAVYEPVP EGIYSEKVTD TISRCLTPDA EARPDIVEVS
781 SMISDVMMKY LDNLSTSQLS LEKKLERERR RTQRYFMEAN RNTVTCHHEL AVLSHETFEK
841 ASLSSSSSGA ASLKSELSES ADLPPEGFQA SYGKDEDRAC DEILSDDNFN LENAEKDTYS
901 EVDDELDISD NSSSSSSSPL KESTFNILKR SFSASGGERQ SQTRDFTGGT GSRPRPALLP
961 LDLLLKVPPH MLRAHIKEIE AELVTGWQSH SLPAVILRNL KDHGPQMGTF LWQASAGIAV
1021 SQRKVRQISD PIQQILIQLH KIIYITQLPP ALHHNLKRRV IERFKKSLFS QQSNPCNLKS
1081 EIKKLSQGSP EPIEPNFFTA DYHLLHRSSG GNSLSPNDPT GLPTSIELEE GITYEQMQTV
1141 IEEVLEESGY YNFTSNRYHS YPWGTKNHPT KRLocalizationUniProt · AlphaFold · HPA
Whether an antibody against NEK10 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
- Secreted
- Secreted
- Yes
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.36
- Highest tissue expression
- 33 nTPM
Expression across tissuesHPA
Tissue
- testis: 33 nTPM
- tongue: 14 nTPM
- breast: 9.8 nTPM
- skeletal muscle: 9.1 nTPM
- fallopian tube: 8.4 nTPM
- epididymis: 5.7 nTPM
Single-cell type
- respiratory ciliated cells: 1,482 nCPM
- ependymal cells: 820 nCPM
- endometrial ciliated cells: 559 nCPM
- myonuclei: 553 nCPM
- fallopian tube ciliated cells: 535 nCPM
- cone photoreceptor cells: 443 nCPM
Immune cell
- neutrophil: 0.2 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
Brain region
- hippocampal formation: 30 nTPM
- cerebral cortex: 29 nTPM
- midbrain: 23 nTPM
- hypothalamus: 23 nTPM
- basal ganglia: 22 nTPM
- choroid plexus: 20 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about NEK10.
Disease | AllUniProt
Conditions NEK10 is implicated in, by any mechanism.
- Ciliary dyskinesia, primary, 44 (CILD44) MIM:618781
Disease | GeneticClinVar
11 pathogenic / likely-pathogenic of 113 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Ciliary dyskinesia, primary, 44
- Primary ciliary dyskinesia
Disease | ImmuneIEDB
Conditions an epitope on NEK10 was assayed in.
- narcolepsy B cell
- multiple sclerosis B cell
- peripheral nervous system disease B cell
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)
- 0.74
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.62
- DepMap mean gene effect
- -0.07
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- mucociliary clearance
- positive regulation of MAP kinase activity
- positive regulation of protein autophosphorylation
- protein phosphorylation
- regulation of cell cycle G2/M phase transition
- regulation of ERK1 and ERK2 cascade
Molecular functions
- ATP binding
- metal ion binding
- protein kinase activity
- protein serine kinase activity
- protein serine/threonine kinase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Protein kinase domain
- Tyrosine-protein kinase, active site
- Protein kinase-like domain superfamily
- Armadillo-like helical
- Armadillo-type fold
- Protein kinase, ATP binding site
- Protein kinase domain
- Serine/threonine-protein kinase Nek10, catalytic domain
- NEK Serine/Threonine Protein Kinase
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of NEK10 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 NEK10 as an antibody target. Whether an autoantibody or antibody against NEK10 could matter depends on whether native NEK10 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
NEK10 is annotated as secreted, so native NEK10 circulates and is directly accessible to antibodies. Secreted and cell-surface proteins are the autoantibody targets most likely to act like drugs, blocking or depleting the native protein.
Annotation status
The present source text does not explicitly label NEK10 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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