NKIRAS2
NF-kappa-B inhibitor-interacting Ras-like protein 2
Also known as: DKFZP434N1526, kappaB-Ras2, KBRAS2, KBRS2_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9NYR9
- Gene
- NKIRAS2
- Ensembl
- ENSG00000168256
- Chromosome
- 17
- Canonical length
- 191 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Nucleoli
OverviewNCBI Gene
Predicted to enable GTPase activating protein binding activity. Predicted to be involved in Ral protein signal transduction. Predicted to act upstream of or within several processes, including lung alveolus development; regulation of signal transduction; and surfactant homeostasis. Predicted to be located in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
191 residues, UniProt reviewed canonical sequence.
>Q9NYR9|NKIRAS2
1 MGKSCKVVVC GQASVGKTSI LEQLLYGNHV VGSEMIETQE DIYVGSIETD RGVREQVRFY
61 DTRGLRDGAE LPRHCFSCTD GYVLVYSTDS RESFQRVELL KKEIDKSKDK KEVTIVVLGN
121 KCDLQEQRRV DPDVAQHWAK SEKVKLWEVS VADRRSLLEP FVYLASKMTQ PQSKSAFPLS
181 RKNKGSGSLD GLocalizationUniProt · AlphaFold · HPA
Whether an antibody against NKIRAS2 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)
- 0.34
- Highest tissue expression
- 47 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 47 nTPM
- heart muscle: 43 nTPM
- esophagus: 35 nTPM
- tongue: 34 nTPM
- placenta: 32 nTPM
- blood vessel: 28 nTPM
Single-cell type
- esophageal apical cells: 122 nCPM
- megakaryocytes: 80 nCPM
- syncytiotrophoblasts: 78 nCPM
- cytotrophoblasts: 63 nCPM
- late primary spermatocytes: 54 nCPM
- migrating cytotrophoblasts: 52 nCPM
Immune cell
- basophil: 54 nTPM
- classical monocyte: 54 nTPM
- non-classical monocyte: 50 nTPM
- plasmacytoid DC: 48 nTPM
- eosinophil: 46 nTPM
- intermediate monocyte: 45 nTPM
Brain region
- basal ganglia: 31 nTPM
- thalamus: 29 nTPM
- cerebral cortex: 28 nTPM
- choroid plexus: 27 nTPM
- medulla oblongata: 27 nTPM
- cerebellum: 26 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)
- 1.01
- gnomAD pLI
- 0.01
- gnomAD missense Z
- 1.03
- DepMap mean gene effect
- -0.04
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 7% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- inflammatory response
- lung alveolus development
- negative regulation of canonical NF-kappaB signal transduction
- Ral protein signal transduction
- regulation of tumor necrosis factor-mediated signaling pathway
- surfactant homeostasis
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of NKIRAS2 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 NKIRAS2 as an antibody target. Whether an autoantibody or antibody against NKIRAS2 could matter depends on whether native NKIRAS2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
NKIRAS2 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 NKIRAS2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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