JKAMP
JNK1/MAPK8-associated membrane protein
Also known as: C14orf100, CDA06, HSPC213, HSPC327, JAMP, JKAMP_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9P055
- Gene
- JKAMP
- Ensembl
- ENSG00000050130
- Chromosome
- 14
- Canonical length
- 311 aa
- Protein class
- Cancer-related genes, Predicted membrane proteins
- Subcellular location
- Nucleoplasm,Vesicles
OverviewNCBI Gene
Enables ubiquitin protein ligase binding activity. Involved in ERAD pathway. Predicted to be located in endoplasmic reticulum membrane. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
311 residues, UniProt reviewed canonical sequence.
>Q9P055|JKAMP
1 MAVDIQPACL GLYCGKTLLF KNGSTEIYGE CGVCPRGQRT NAQKYCQPCT ESPELYDWLY
61 LGFMAMLPLV LHWFFIEWYS GKKSSSALFQ HITALFECSM AAIITLLVSD PVGVLYIRSC
121 RVLMLSDWYT MLYNPSPDYV TTVHCTHEAV YPLYTIVFIY YAFCLVLMML LRPLLVKKIA
181 CGLGKSDRFK SIYAALYFFP ILTVLQAVGG GLLYYAFPYI ILVLSLVTLA VYMSASEIEN
241 CYDLLVRKKR LIVLFSHWLL HAYGIISISR VDKLEQDLPL LALVPTPALF YLFTAKFTEP
301 SRILSEGANG HLocalizationUniProt · AlphaFold · HPA
Whether an antibody against JKAMP 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
- 7
- Mean surface accessibility (rSASA)
- 0.32
- Highest tissue expression
- 53 nTPM
Expression across tissuesHPA
Tissue
- parathyroid gland: 53 nTPM
- kidney: 41 nTPM
- choroid plexus: 39 nTPM
- spinal cord: 35 nTPM
- adrenal gland: 33 nTPM
- thyroid gland: 32 nTPM
Single-cell type
- late primary spermatocytes: 206 nCPM
- early spermatids: 170 nCPM
- kupffer cells: 96 nCPM
- extravillous trophoblasts: 88 nCPM
- fallopian tube ciliated cells: 87 nCPM
- late spermatids: 83 nCPM
Immune cell
- neutrophil: 90 nTPM
- basophil: 87 nTPM
- non-classical monocyte: 83 nTPM
- eosinophil: 82 nTPM
- intermediate monocyte: 75 nTPM
- plasmacytoid DC: 71 nTPM
Brain region
- choroid plexus: 47 nTPM
- pons: 41 nTPM
- white matter: 41 nTPM
- hypothalamus: 38 nTPM
- medulla oblongata: 38 nTPM
- midbrain: 37 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about JKAMP.
Disease | GeneticClinVar
4 pathogenic / likely-pathogenic of 46 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Neurodevelopmental disorder with seizures and impaired intellectual and language development
- JKAMP-associated neurodevelopmental disease
- JKAMP neurodevelopmental disorder
- JKAMP-related neurodevelopmental disorder
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)
- 0.62
- gnomAD pLI
- 0.08
- gnomAD missense Z
- 1.55
- DepMap mean gene effect
- -0.14
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- JNK1/MAPK8-associated membrane protein
- JNK1/MAPK8-associated membrane protein
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of JKAMP 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 JKAMP as an antibody target. Whether an autoantibody or antibody against JKAMP could matter depends on whether native JKAMP is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
JKAMP 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 JKAMP as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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