IKBIP
Inhibitor of nuclear factor kappa-B kinase-interacting protein
Also known as: FLJ31051, IKIP, IKIP_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q70UQ0
- Gene
- IKBIP
- Ensembl
- ENSG00000166130
- Chromosome
- 12
- Canonical length
- 350 aa
- Protein class
- Predicted intracellular proteins, Predicted membrane proteins
- Subcellular location
- Nucleoli rim,Endoplasmic reticulum
OverviewNCBI Gene
Predicted to be involved in response to X-ray. Predicted to act upstream of or within several processes, including negative regulation of NF-kappaB transcription factor activity; response to interleukin-1; and response to tumor necrosis factor. Located in endoplasmic reticulum and nucleolus. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
350 residues, UniProt reviewed canonical sequence.
>Q70UQ0|IKBIP
1 MSEVKSRKKS GPKGAPAAEP GKRSEGGKTP VARSSGGGGW ADPRTCLSLL SLGTCLGLAW
61 FVFQQSEKFA KVENQYQLLK LETNEFQQLQ SKISLISEKW QKSEAIMEQL KSFQIIAHLK
121 RLQEEINEVK TWSNRITEKQ DILNNSLTTL SQDITKVDQS TTSMAKDVGL KITSVKTDIR
181 RISGLVTDVI SLTDSVQELE NKIEKVEKNT VKNIGDLLSS SIDRTATLRK TASENSQRIN
241 SVKKTLTELK SDFDKHTDRF LSLEGDRAKV LKTVTFANDL KPKVYNLKKD FSRLEPLVND
301 LTLRIGRLVT DLLQREKEIA FLSEKISNLT IVQAEIKDIK DEIAHISDMNLocalizationUniProt · AlphaFold · HPA
Whether an antibody against IKBIP 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
- Other membrane
- Secreted
- No
- Transmembrane segments
- 1
- Mean surface accessibility (rSASA)
- 0.53
- Highest tissue expression
- 25 nTPM
Expression across tissuesHPA
Tissue
- placenta: 25 nTPM
- urinary bladder: 16 nTPM
- smooth muscle: 15 nTPM
- appendix: 15 nTPM
- adipose tissue: 14 nTPM
- blood vessel: 12 nTPM
Single-cell type
- neutrophils: 166 nCPM
- plasma cells: 108 nCPM
- extravillous trophoblasts: 98 nCPM
- hepatic stellate cells: 78 nCPM
- monocyte progenitors: 77 nCPM
- decidual stromal cells: 76 nCPM
Immune cell
- neutrophil: 28 nTPM
- eosinophil: 19 nTPM
- basophil: 11 nTPM
- classical monocyte: 6.4 nTPM
- memory B-cell: 6 nTPM
- non-classical monocyte: 5.7 nTPM
Brain region
- choroid plexus: 8.3 nTPM
- white matter: 5.7 nTPM
- medulla oblongata: 4.8 nTPM
- thalamus: 4.6 nTPM
- hypothalamus: 4.2 nTPM
- spinal cord: 4.1 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)
- 1.39
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.2
- DepMap mean gene effect
- -0.06
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Inhibitor of nuclear factor kappa-B kinase-interacting protein
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of IKBIP 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 IKBIP as an antibody target. Whether an autoantibody or antibody against IKBIP could matter depends on whether native IKBIP is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
IKBIP 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 IKBIP as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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