Gene Gene information from NCBI Gene database.
Entrez ID 10266
Gene name Receptor activity modifying protein 2
Gene symbol RAMP2
Synonyms (NCBI Gene)
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Chromosome 17
Chromosome location 17q21.2
Summary The protein encoded by this gene is a member of the RAMP family of single-transmembrane-domain proteins, called receptor (calcitonin) activity modifying proteins (RAMPs). RAMPs are type I transmembrane proteins with an extracellular N terminus and a cytop
miRNA miRNA information provided by mirtarbase database.
9
miRTarBase ID miRNA Experiments Reference
MIRT1289326 hsa-miR-1255a CLIP-seq
MIRT1289327 hsa-miR-1255b CLIP-seq
MIRT1289328 hsa-miR-4450 CLIP-seq
MIRT1289329 hsa-miR-4693-3p CLIP-seq
MIRT1289330 hsa-miR-4712-3p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
67
GO ID Ontology Definition Evidence Reference
GO:0001525 Process Angiogenesis IBA
GO:0001525 Process Angiogenesis IDA 20596610
GO:0001570 Process Vasculogenesis IMP 16964401
GO:0001605 Function Adrenomedullin receptor activity IPI 9620797, 20074556, 22102369
GO:0002040 Process Sprouting angiogenesis IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
605154 9844 ENSG00000131477
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
O60895
Protein name Receptor activity-modifying protein 2 (Calcitonin-receptor-like receptor activity-modifying protein 2) (CRLR activity-modifying protein 2)
Protein function Accessory protein that interacts with and modulates the function of G-protein coupled receptors including calcitonin gene-related peptide type 1 receptor (CALCRL) and calcitonin receptor (CALCR) (PubMed:9620797). Required for the transport of CA
PDB 2XVT , 3AQE , 3AQF , 4RWF , 6UUN , 6V2E , 7TYH , 7TYX , 7TYY
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF04901 RAMP 65 173 Receptor activity modifying family Family
Tissue specificity TISSUE SPECIFICITY: Strongly expressed in lung, breast, immune system and fetal tissues. {ECO:0000269|PubMed:9620797}.
Sequence
Sequence length 175
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Hormone signaling
Vascular smooth muscle contraction
  G alpha (s) signalling events
Calcitonin-like ligand receptors
ADORA2B mediated anti-inflammatory cytokines production
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
1
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
RAMP2-related disorder Likely benign rs568718402 RCV003902120
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Adenocarcinoma of Lung Associate 36032660
Arthritis Rheumatoid Associate 20942979
Coronary Artery Disease Associate 17878224
Diabetes Gestational Associate 28666334
Fetal Growth Retardation Associate 27258937
Hyperoxia Stimulate 34911614
Lung Injury Associate 34911614
Obesity Associate 34271220
Panniculitis Peritoneal Associate 27258937
Reperfusion Injury Associate 22183724