NCKAP1
Nck-associated protein 1
Also known as: HEM2, Nap1, NAP125, NCKP1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9Y2A7
- Gene
- NCKAP1
- Ensembl
- ENSG00000061676
- Chromosome
- 2
- Canonical length
- 1128 aa
- Protein class
- Predicted membrane proteins
- Subcellular location
- Cytosol
OverviewNCBI Gene
Contributes to small GTPase binding activity. Involved in Rac protein signal transduction; positive regulation of Arp2/3 complex-mediated actin nucleation; and positive regulation of lamellipodium assembly. Located in extracellular exosome and focal adhesion. Part of SCAR complex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
1128 residues, UniProt reviewed canonical sequence.
>Q9Y2A7|NCKAP1
1 MSRSVLQPSQ QKLAEKLTIL NDRGVGMLTR LYNIKKACGD PKAKPSYLID KNLESAVKFI
61 VRKFPAVETR NNNQQLAQLQ KEKSEILKNL ALYYFTFVDV MEFKDHVCEL LNTIDVCQVF
121 FDITVNFDLT KNYLDLIITY TTLMILLSRI EERKAIIGLY NYAHEMTHGA SDREYPRLGQ
181 MIVDYENPLK KMMEEFVPHS KSLSDALISL QMVYPRRNLS ADQWRNAQLL SLISAPSTML
241 NPAQSDTMPC EYLSLDAMEK WIIFGFILCH GILNTDATAL NLWKLALQSS SCLSLFRDEV
301 FHIHKAAEDL FVNIRGYNKR INDIRECKEA AVSHAGSMHR ERRKFLRSAL KELATVLSDQ
361 PGLLGPKALF VFMALSFARD EIIWLLRHAD NMPKKSADDF IDKHIAELIF YMEELRAHVR
421 KYGPVMQRYY VQYLSGFDAV VLNELVQNLS VCPEDESIIM SSFVNTMTSL SVKQVEDGEV
481 FDFRGMRLDW FRLQAYTSVS KASLGLADHR ELGKMMNTII FHTKMVDSLV EMLVETSDLS
541 IFCFYSRAFE KMFQQCLELP SQSRYSIAFP LLCTHFMSCT HELCPEERHH IGDRSLSLCN
601 MFLDEMAKQA RNLITDICTE QCTLSDQLLP KHCAKTISQA VNKKSKKQTG KKGEPEREKP
661 GVESMRKNRL VVTNLDKLHT ALSELCFSIN YVPNMVVWEH TFTPREYLTS HLEIRFTKSI
721 VGMTMYNQAT QEIAKPSELL TSVRAYMTVL QSIENYVQID ITRVFNNVLL QQTQHLDSHG
781 EPTITSLYTN WYLETLLRQV SNGHIAYFPA MKAFVNLPTE NELTFNAEEY SDISEMRSLS
841 ELLGPYGMKF LSESLMWHIS SQVAELKKLV VENVDVLTQM RTSFDKPDQM AALFKRLSSV
901 DSVLKRMTII GVILSFRSLA QEALRDVLSY HIPFLVSSIE DFKDHIPRET DMKVAMNVYE
961 LSSAAGLPCE IDPALVVALS SQKSENISPE EEYKIACLLM VFVAVSLPTL ASNVMSQYSP
1021 AIEGHCNNIH CLAKAINQIA AALFTIHKGS IEDRLKEFLA LASSSLLKIG QETDKTTTRN
1081 RESVYLLLDM IVQESPFLTM DLLESCFPYV LLRNAYHAVY KQSVTSSALocalizationUniProt · AlphaFold · HPA
Whether an antibody against NCKAP1 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
- 1
- Mean surface accessibility (rSASA)
- 0.24
- Highest tissue expression
- 84 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 84 nTPM
- parathyroid gland: 83 nTPM
- blood vessel: 83 nTPM
- cerebral cortex: 82 nTPM
- tongue: 81 nTPM
- thyroid gland: 80 nTPM
Single-cell type
- esophageal apical cells: 450 nCPM
- pituicytes/fscs: 336 nCPM
- parietal cells: 292 nCPM
- bergmann glia: 277 nCPM
- retinal pigment epithelial cells: 273 nCPM
- cardiomyocytes: 257 nCPM
Immune cell
- T-reg: 0.2 nTPM
- basophil: 0.1 nTPM
- gdT-cell: 0.1 nTPM
- MAIT T-cell: 0.1 nTPM
- memory CD4 T-cell: 0.1 nTPM
- memory CD8 T-cell: 0.1 nTPM
Brain region
- hippocampal formation: 149 nTPM
- cerebral cortex: 122 nTPM
- basal ganglia: 114 nTPM
- hypothalamus: 95 nTPM
- midbrain: 94 nTPM
- thalamus: 91 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about NCKAP1.
Disease | GeneticClinVar
24 pathogenic / likely-pathogenic of 232 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Neurodevelopmental disorder
- Global developmental delay
- Autistic behavior
- NCKAP1-associated Neurodevelopmental disorder
- Inborn genetic diseases
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)
- 0.04
- gnomAD pLI
- 1
- gnomAD missense Z
- 4.27
- DepMap mean gene effect
- -0.48
- 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
- apical protein localization
- apoptotic process
- basal protein localization
- cell migration
- cell migration involved in gastrulation
- cell morphogenesis
- cell projection assembly
- central nervous system development
- cortical actin cytoskeleton organization
- embryonic body morphogenesis
- embryonic foregut morphogenesis
- embryonic heart tube development
- endoderm development
- establishment or maintenance of actin cytoskeleton polarity
- in utero embryonic development
- lamellipodium assembly
- mesodermal cell migration
- neural tube closure
- neuron projection morphogenesis
- notochord morphogenesis
- paraxial mesoderm morphogenesis
- positive regulation of actin filament polymerization
- positive regulation of Arp2/3 complex-mediated actin nucleation
- positive regulation of lamellipodium assembly
- protein stabilization
- Rac protein signal transduction
- regulation of protein localization
- somitogenesis
- zygotic determination of anterior/posterior axis, embryo
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of NCKAP1 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 NCKAP1 as an antibody target. Whether an autoantibody or antibody against NCKAP1 could matter depends on whether native NCKAP1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
NCKAP1 is annotated at the cell surface, where native NCKAP1 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 NCKAP1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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