Gene Gene information from NCBI Gene database.
Entrez ID 59082
Gene name Caspase recruitment domain family member 18
Gene symbol CARD18
Synonyms (NCBI Gene)
ICEBERGUNQ5804pseudo-ICE
Chromosome 11
Chromosome location 11q22.3
miRNA miRNA information provided by mirtarbase database.
21
miRTarBase ID miRNA Experiments Reference
MIRT862784 hsa-miR-1321 CLIP-seq
MIRT862785 hsa-miR-3126-5p CLIP-seq
MIRT862786 hsa-miR-3153 CLIP-seq
MIRT862787 hsa-miR-3202 CLIP-seq
MIRT862788 hsa-miR-4476 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
15
GO ID Ontology Definition Evidence Reference
GO:0004197 Function Cysteine-type endopeptidase activity IEA
GO:0004869 Function Cysteine-type endopeptidase inhibitor activity IEA
GO:0005515 Function Protein binding IPI 11536016, 15383541, 27043298
GO:0006508 Process Proteolysis IEA
GO:0006954 Process Inflammatory response NAS 11051551
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
605354 28861 ENSG00000255501
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P57730
Protein name Caspase recruitment domain-containing protein 18 (Caspase-1 inhibitor Iceberg)
Protein function Inhibits generation of IL-1-beta by interacting with caspase-1 and preventing its association with RIP2. Down-regulates the release of IL1B.
PDB 1DGN
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00619 CARD 3 90 Caspase recruitment domain Domain
Tissue specificity TISSUE SPECIFICITY: Primarily expressed in the heart and placenta. {ECO:0000269|PubMed:11051551}.
Sequence
Sequence length 90
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG 
  NOD-like receptor signaling pathway  
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
5
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
ALZHEIMER DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CARCINOMA, NON-SMALL-CELL LUNG CTD
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CARCINOMA, SQUAMOUS CELL CTD
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
DIABETIC RETINOPATHY GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Esophageal Squamous Cell Carcinoma Associate 35789548
★☆☆☆☆
Found in Text Mining only
Hypoxia Associate 35789548
★☆☆☆☆
Found in Text Mining only