Gene Gene information from NCBI Gene database.
Entrez ID 130132
Gene name Raftlin family member 2
Gene symbol RFTN2
Synonyms (NCBI Gene)
C2orf11Raftlin-2
Chromosome 2
Chromosome location 2q33.1
miRNA miRNA information provided by mirtarbase database.
134
miRTarBase ID miRNA Experiments Reference
MIRT017859 hsa-miR-335-5p Microarray 18185580
MIRT648585 hsa-miR-4310 HITS-CLIP 23824327
MIRT648584 hsa-miR-7157-5p HITS-CLIP 23824327
MIRT648583 hsa-miR-338-3p HITS-CLIP 23824327
MIRT648582 hsa-miR-4645-5p HITS-CLIP 23824327
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:0005515 Function Protein binding IPI 32296183
GO:0005886 Component Plasma membrane IEA
GO:0016020 Component Membrane IEA
GO:0033227 Process DsRNA transport IEA
GO:0043330 Process Response to exogenous dsRNA IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
618215 26402 ENSG00000162944
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q52LD8
Protein name Raftlin-2 (Raft-linking protein 2)
Protein function Upon bacterial lipopolysaccharide stimulation, mediates clathrin-dependent internalization of TLR4 in dendritic cells, resulting in activation of TICAM1-mediated signaling and subsequent IFNB1 production. May regulate B-cell antigen receptor-med
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15250 Raftlin 1 440 Raftlin Family
Sequence
Sequence length 501
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
15
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
ATOPIC ASTHMA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
BIPOLAR DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CROHN'S DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
DILATED CARDIOMYOPATHY GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Non alcoholic Fatty Liver Disease Associate 35188871
★☆☆☆☆
Found in Text Mining only