Gene Gene information from NCBI Gene database.
Entrez ID 245812
Gene name Canopy FGF signaling regulator 4
Gene symbol CNPY4
Synonyms (NCBI Gene)
PRAT4B
Chromosome 7
Chromosome location 7q22.1
miRNA miRNA information provided by mirtarbase database.
43
miRTarBase ID miRNA Experiments Reference
MIRT005173 hsa-miR-30a-5p pSILAC 18668040
MIRT005173 hsa-miR-30a-5p Proteomics;Other 18668040
MIRT901330 hsa-miR-1289 CLIP-seq
MIRT901331 hsa-miR-3198 CLIP-seq
MIRT901332 hsa-miR-329 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
5
GO ID Ontology Definition Evidence Reference
GO:0005102 Function Signaling receptor binding IBA
GO:0005102 Function Signaling receptor binding IEA
GO:0005515 Function Protein binding IPI 28514442, 32296183, 33961781
GO:0005576 Component Extracellular region IEA
GO:1903078 Process Positive regulation of protein localization to plasma membrane IMP 16338228
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
610047 28631 ENSG00000166997
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8N129
Protein name Protein canopy homolog 4
Protein function Plays a role in the regulation of the cell surface expression of TLR4.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF11938 DUF3456 37 196 TLR4 regulator and MIR-interacting MSAP Family
Sequence
Sequence length 248
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
3
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
CORONARY ARTERY DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
GOUT GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
LIVER CIRRHOSIS, EXPERIMENTAL CTD
★★☆☆☆
Found in Text Mining + Unknown/Other Associations