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Gene Symbol |
CALCA |
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Aliases |
CALC1, CGRP, CGRP-I, CGRP1, CT, KC, PCT |
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Entrez Gene ID |
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Gene Name |
Calcitonin related polypeptide alpha |
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Chromosomal Location |
11p15.2 |
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HGNC ID |
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Summary |
This gene encodes the peptide hormones calcitonin, calcitonin gene-related peptide and katacalcin by tissue-specific alternative RNA splicing of the gene transcripts and cleavage of inactive precursor proteins. Calcitonin is involved in calcium regulation and acts to regulate phosphorus metabolism. Calcitonin gene-related peptide functions as a vasodilator and as an antimicrobial peptide while katacalcin is a calcium-lowering peptide. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Aug 2014]
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RefSeq DNA |
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RefSeq mRNA |
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e!Ensembl
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Protein Information |
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Protein Name |
Calcitonin, calcitonin gene-related peptide 1, alpha-type CGRP, calcitonin 1, calcitonin gene-related peptide I, calcitonin/calcitonin-related polypeptide, alpha, katacalcin |
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Function |
CGRP induces vasodilation. It dilates a variety of vessels including the coronary, cerebral and systemic vasculature. Its abundance in the CNS also points toward a neurotransmitter or neuromodulator role. It also elevates platelet cAMP. |
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UniProt |
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PDB |
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Pfam |
Pfam Accession |
Pfam ID |
PF00214 |
Calc_CGRP_IAPP |
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Interactions |
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STRING |
MINT |
IntAct |
ENSP00000310928 |
Q03181 |
Q03181 |
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View interactions
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Associated Diseases
Disease group | Disease Name | References |
Cardiovascular Diseases |
Hypertensive disease |
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Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
Catalepsy |
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Down Syndrome |
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Endocrine System Diseases |
PCOS |
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Musculoskeletal Diseases |
Arthritis |
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Osteoarthrosis Deformans |
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Neoplasms |
Prostate cancer |
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Nervous System Diseases |
Sciatic Neuritis |
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Neuralgia |
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Migraine |
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Trigeminal neuralgia |
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Sick Headaches |
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Neuropathy |
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Nutritional and Metabolic Diseases |
Hypercalcemia |
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Milk-Alkali Syndrome |
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Psychiatric/Brain disorders |
Bipolar Disorder |
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Intellectual Disability |
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Autistic Disorder |
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Obstructive Sleep Apnea |
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Reproductive disorders |
Preeclampsia |
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Respiratory Tract Diseases |
Pulmonary Fibrosis |
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Bronchial hyperreactivity |
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References |
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PubMed ID |
Associated gene/s |
Associated condition |
Genetic Mutation |
Diagnostic Criteria |
Association with PCOS |
Ethnicity |
Conclusion |
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E(2) |
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Related
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The present findings suggest that CGRP may participate in the pathophysiological process of PCOS. |
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