Gene Gene information from NCBI Gene database.
Entrez ID 51528
Gene name JNK1/MAPK8 associated membrane protein
Gene symbol JKAMP
Synonyms (NCBI Gene)
C14orf100C24orf100CDA06HSPC213HSPC327JAMP
Chromosome 14
Chromosome location 14q23.1
miRNA miRNA information provided by mirtarbase database.
303
miRTarBase ID miRNA Experiments Reference
MIRT571387 hsa-miR-7849-3p PAR-CLIP 20371350
MIRT571386 hsa-miR-2115-3p PAR-CLIP 20371350
MIRT571385 hsa-miR-4307 PAR-CLIP 20371350
MIRT571384 hsa-miR-125b-2-3p PAR-CLIP 20371350
MIRT571383 hsa-miR-567 PAR-CLIP 20371350
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
9
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 32296183
GO:0005783 Component Endoplasmic reticulum IEA
GO:0005789 Component Endoplasmic reticulum membrane IEA
GO:0006986 Process Response to unfolded protein IEA
GO:0016020 Component Membrane IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
611176 20184 ENSG00000050130
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9P055
Protein name JNK1/MAPK8-associated membrane protein (JKAMP) (JNK1-associated membrane protein) (JAMP) (Medulloblastoma antigen MU-MB-50.4)
Protein function Regulates the duration of MAPK8 activity in response to various stress stimuli (By similarity). Facilitates degradation of misfolded endoplasmic reticulum (ER) proteins through the recruitment of components of the proteasome and endoplasmic reti
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF05571 JAMP 17 308 JNK1/MAPK8-associated membrane protein Family
Sequence
Sequence length 311
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
SCHIZOPHRENIA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations