Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
10203
Gene name Gene Name - the full gene name approved by the HGNC.
Calcitonin receptor like receptor
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
CALCRL
Synonyms (NCBI Gene) Gene synonyms aliases
CGRPR, CRLR, LMPHM8
Chromosome Chromosome number
2
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
2q32.1
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT022193 hsa-miR-124-3p Microarray 18668037
MIRT858953 hsa-miR-1226 CLIP-seq
MIRT858954 hsa-miR-1244 CLIP-seq
MIRT858955 hsa-miR-128 CLIP-seq
MIRT858956 hsa-miR-1287 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:0001605 Function Adrenomedullin receptor activity IBA
GO:0001605 Function Adrenomedullin receptor activity IDA 9620797, 32296767
GO:0001605 Function Adrenomedullin receptor activity IPI 9620797, 10882736, 20074556, 22102369
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
114190 16709 ENSG00000064989
Protein
UniProt ID Q16602
Protein name Calcitonin gene-related peptide type 1 receptor (CGRP type 1 receptor) (Calcitonin receptor-like receptor) (CRLR)
Protein function G protein-coupled receptor which specificity is determined by its interaction with receptor-activity-modifying proteins (RAMPs) (PubMed:32296767, PubMed:33602864, PubMed:8626685). Together with RAMP1, form the receptor complex for calcitonin-gen
PDB 3AQF , 3N7P , 3N7R , 3N7S , 4RWF , 4RWG , 5V6Y , 6D1U , 6E3Y , 6UMG , 6UUN , 6UUS , 6UVA , 6V2E , 6ZHO , 6ZIS , 7KNT , 7KNU , 7P0F , 7P0I , 8AX5 , 8AX6 , 8AX7
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF02793 HRM 62 130 Hormone receptor domain Family
PF00002 7tm_2 138 380 7 transmembrane receptor (Secretin family) Family
Tissue specificity TISSUE SPECIFICITY: Predominantly expressed in the lung and heart. {ECO:0000269|PubMed:8626685}.
Sequence
Sequence length 461
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Neuroactive ligand-receptor interaction
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)
Causal Diseases caused by PATHOGENIC or LIKELY PATHOGENIC variants from ClinVar only
Disease merge term Disease name dbSNP ID References
Lymphatic Malformation Lymphatic malformation 8 rs1574226259 N/A
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
Anxiety Disorder Anxiety N/A N/A GWAS
Carcinoma Basal cell carcinoma N/A N/A GWAS
Coronary artery disease Coronary artery disease N/A N/A GWAS
Coronary Heart Disease Coronary heart disease N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Adenocarcinoma of Lung Associate 34039311, 36032660
Anemia Associate 33413630
Anxiety Disorders Associate 32507125
Arthritis Psoriatic Associate 35806402
Arthritis Rheumatoid Associate 10555038
Carcinoma Hepatocellular Associate 36785674
Carcinoma Renal Cell Associate 23969937
Cell Transformation Neoplastic Associate 14747444
Coronary Artery Disease Associate 38602103
Diabetes Gestational Associate 28666334