Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
10266
Gene name Gene Name - the full gene name approved by the HGNC.
Receptor activity modifying protein 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
RAMP2
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
17
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
17q21.2
Summary Summary of gene provided in NCBI Entrez Gene.
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.
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 information of associated ontologies with gene provided by GO database.
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 ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
605154 9844 ENSG00000131477
Protein
UniProt ID 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
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Diabetes Type 2 diabetes N/A N/A GWAS
Glaucoma open-angle glaucoma N/A N/A GenCC
Associations from Text Mining Disease 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