NEK7
Serine/threonine-protein kinase Nek7
Also known as: NEK7_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8TDX7
- Gene
- NEK7
- Ensembl
- ENSG00000151414
- Chromosome
- 1
- Canonical length
- 302 aa
- Protein class
- Enzymes, Predicted intracellular proteins, Transporters
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
NIMA-related kinases share high amino acid sequence identity with the gene product of the Aspergillus nidulans 'never in mitosis A' gene, which controls initiation of mitosis.[supplied by OMIM, Jul 2002]
Canonical amino-acid sequenceUniProt
302 residues, UniProt reviewed canonical sequence.
>Q8TDX7|NEK7
1 MDEQSQGMQG PPVPQFQPQK ALRPDMGYNT LANFRIEKKI GRGQFSEVYR AACLLDGVPV
61 ALKKVQIFDL MDAKARADCI KEIDLLKQLN HPNVIKYYAS FIEDNELNIV LELADAGDLS
121 RMIKHFKKQK RLIPERTVWK YFVQLCSALE HMHSRRVMHR DIKPANVFIT ATGVVKLGDL
181 GLGRFFSSKT TAAHSLVGTP YYMSPERIHE NGYNFKSDIW SLGCLLYEMA ALQSPFYGDK
241 MNLYSLCKKI EQCDYPPLPS DHYSEELRQL VNMCINPDPE KRPDVTYVYD VAKRMHACTA
301 SSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against NEK7 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)
- 0.28
- Highest tissue expression
- 131 nTPM
Expression across tissuesHPA
Tissue
- heart muscle: 131 nTPM
- adipose tissue: 60 nTPM
- tongue: 60 nTPM
- skeletal muscle: 53 nTPM
- blood vessel: 52 nTPM
- spinal cord: 48 nTPM
Single-cell type
- neutrophils: 794 nCPM
- adrenal cortex cells: 612 nCPM
- cardiomyocytes: 429 nCPM
- ocular epithelial cells: 377 nCPM
- hematopoietic stem cells: 342 nCPM
- monocytes: 289 nCPM
Immune cell
- MAIT T-cell: 13 nTPM
- neutrophil: 6 nTPM
- T-reg: 6 nTPM
- memory CD8 T-cell: 4.1 nTPM
- NK-cell: 3.6 nTPM
- eosinophil: 3.3 nTPM
Brain region
- white matter: 109 nTPM
- medulla oblongata: 105 nTPM
- spinal cord: 104 nTPM
- basal ganglia: 99 nTPM
- hypothalamus: 96 nTPM
- pons: 85 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)
- 0.39
- gnomAD pLI
- 0.88
- gnomAD missense Z
- 2.29
- DepMap mean gene effect
- -0.03
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cellular response to potassium ion
- positive regulation of NLRP3 inflammasome complex assembly
- positive regulation of telomere maintenance
- protein phosphorylation
- regulation of mitotic cell cycle
- spindle assembly
Molecular functions
- ATP binding
- metal ion binding
- molecular function activator activity
- protein serine kinase activity
- protein serine/threonine kinase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of NEK7 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 NEK7 as an antibody target. Whether an autoantibody or antibody against NEK7 could matter depends on whether native NEK7 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
NEK7 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 NEK7 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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