CNK3/IPCEF1
CNK3/IPCEF1 fusion protein
Also known as: CNIPF_HUMAN, ENSG00000288520
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- G9CGD6
- Gene
- CNK3/IPCEF1
- Ensembl
- ENSG00000288520
- Chromosome
- 6
- Canonical length
- 899 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoli,Nuclear speckles,Plasma membrane,Cytoplasmic bodies
OverviewNCBI Gene
No narrative summary is available for CNK3/IPCEF1 in this catalog release; identity and structured annotations are shown without generated factual claims.
Canonical amino-acid sequenceUniProt
899 residues, UniProt reviewed canonical sequence.
>G9CGD6|CNK3/IPCEF1
1 MEPVTKWSPK QVVDWTRGLD DCLQQYVHKF EREKINGEQL LQISHQDLEE LGVTRIGHQE
61 LVLEAVDLLC ALNYGLETDN MKNLVLKLRA SSHNLQNYIS SRRKSPAYDG NTSRKAPNEF
121 LTSVVELIGA AKALLAWLDR APFTGITDFS VTKNKIIQLC LDLTTTVQKD CFVAEMEDKV
181 LTVVKVLNGI CDKTIRSTTD PVMSQCACLE EVHLPNIKPG EGLGMYIKST YDGLHVITGT
241 TENSPADRSQ KIHAGDEVIQ VNQQTVVGWQ LKNLVKKLRE NPTGVVLLLK KRPTGSFNFT
301 PAPLKNLRWK PPLVQTSPPP ATTQSPESTM DTSLKKEKSA ILDLYIPPPP AVPYSPRDEN
361 GSFVYGGSSK CKQPLPGPKG SESPNSFLDQ ESRRRRFTIA DSDQLPGYSV ETNILPTKMR
421 EKTPSYGKPR PLSMPADGNW MGIVDPFARP RGHGRKAFVS TKMTSYMAID GSALVPLRQK
481 PRRKTQGFLT MSRRRISCKD LGHADCQGWL YKKKEKGSFL SNKWKKFWVI LKGSSLYWYS
541 NQMAEKADGF VNLPDFTVER ASECKKKHAF KISHPQIKTF YFAAENVQEM NVWLNKLGSA
601 VIHQESTTKD EECYSESEQE DPEIAAETPP PPHASQTQSL TAQQASSSSP SLSGTSYSFS
661 SLENTVKTPS SFPSSLSKER QSLPDTVNSL SAAEDEGQPI TFAVQVHSPV PSEAGIHKAL
721 ENSFVTSESG FLNSLSSDDT SSLSSNHDHL TVPDKPAGSK IMDKEETKVS EDDEMEKLYK
781 SLEQASLSPL GDRRPSTKKE LRKSFVKRCK NPSINEKLHK IRTLNSTLKC KEHDLAMINQ
841 LLDDPKLTAR KYREWKVMNT LLIQDIYQQQ RASPAPDDTD DTPQELKKSP SSPSVENSILocalizationUniProt · AlphaFold · HPA
Whether an antibody against CNK3/IPCEF1 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)
- 0.49
- Highest tissue expression
- 1.3 nTPM
Expression across tissuesHPA
Tissue
- pancreas: 1.3 nTPM
- esophagus: 0.9 nTPM
- kidney: 0.9 nTPM
- choroid plexus: 0.8 nTPM
- endometrium: 0.7 nTPM
- liver: 0.7 nTPM
Single-cell type
- endometrial luminal cells: 61 nCPM
- endometrial glandular cells: 35 nCPM
- endometrial ciliated cells: 29 nCPM
- epididymal clear cells: 29 nCPM
- retinal pigment epithelial cells: 21 nCPM
- myosatellite cells: 17 nCPM
Immune cell
- eosinophil: 0.2 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- white matter: 2.2 nTPM
- choroid plexus: 1.6 nTPM
- cerebral cortex: 1.4 nTPM
- medulla oblongata: 1.4 nTPM
- cerebellum: 1.3 nTPM
- pons: 1.3 nTPM
OntologyGO
Biological processes
- regulation of signal transduction
- positive regulation of cellular response to hepatocyte growth factor stimulus
Cellular components
Protein domainsUniProt · Pfam · InterPro
- PDZ domain
- Sterile alpha motif domain
- Pleckstrin homology domain
- Connector enhancer of kinase suppressor of ras 2/3 domain
- PH-like domain superfamily
- Sterile alpha motif/pointed domain superfamily
- CRIC domain
- PDZ superfamily
- CNK1-3, SAM domain
- Connector enhancer of kinase suppressor of Ras
- PH domain
- SAM domain (Sterile alpha motif)
- PDZ domain
- Connector enhancer of kinase suppressor of ras 2/3 domain
- Connector enhancer of kinase suppressor of ras
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads CNK3/IPCEF1 as an antibody target. Whether an autoantibody or antibody against CNK3/IPCEF1 could matter depends on whether native CNK3/IPCEF1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CNK3/IPCEF1 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 CNK3/IPCEF1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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