Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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808
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Gene name
Gene Name - the full gene name approved by the HGNC.
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Calmodulin 3 |
Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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CALM3 |
Synonyms (NCBI Gene)
Gene synonyms aliases
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CALM, CAM1, CAM2, CAMB, CPVT6, CaM, CaMIII, HEL-S-72, LQT16, PHKD, PHKD3 |
Disease Acronyms (UniProt)
Disease acronyms from UniProt database
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CPVT6, LQT16 |
Chromosome
Chromosome number
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19 |
Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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19q13.32 |
Summary
Summary of gene provided in NCBI Entrez Gene.
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This gene encodes a member of a family of proteins that binds calcium and functions as a enzymatic co-factor. Activity of this protein is important in the regulation of the cell cycle and cytokinesis. Multiple alternatively spliced transcript variants hav |
Causal |
Disease term |
Disease name |
dbSNP ID |
References |
Catecholaminergic polymorphic ventricular tachycardia |
VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1 (disorder), Catecholaminergic polymorphic ventricular tachycardia |
rs121918597, rs121918598, rs121918599, rs121918600, rs121918601, rs121918602, rs121918603, rs121918604, rs121918605, rs121434549, rs786205106, rs121434550, rs267607276, rs267607277, rs397507555, rs397507556, rs397516508, rs397516539, rs397516643, rs768049331, rs397515458, rs397515459, rs730880187, rs730880201, rs1553191909, rs139228801, rs786205791, rs786205799, rs794728706, rs794728708, rs190140598, rs794728721, rs794728740, rs794728746, rs794728753, rs794728754, rs794728756, rs794728704, rs794728777, rs794728779, rs794728782, rs794728783, rs794728785, rs771994461, rs794728786, rs794728787, rs794728803, rs794728804, rs794728810, rs794728811, rs794728832, rs763955301, rs1085307100, rs876657635, rs886037908, rs886037907, rs1057517699, rs773204795, rs1060502164, rs1060500142, rs1060500156, rs1060500150, rs1060500137, rs1060502114, rs1060502116, rs1064796516, rs1085307997, rs776874142, rs1436844070, rs1553322494, rs1553197939, rs1553343100, rs752256846, rs865784613, rs1553454821, rs1553426678, rs1415931588, rs1553263875, rs794728802, rs1553339086, rs1554258777, rs756636650, rs905985075, rs1401116572, rs1553339084, rs1553531703, rs1554251609, rs1558405887, rs1558698334, rs1558393802, rs1558405816, rs397516510, rs1558481148, rs1558424746, rs1558103974, rs1558381851, rs1558405653, rs1468290898, rs1573911397, rs1471576368, rs375598471, rs1342435908, rs1573300872, rs1209752961, rs1573887621, rs1226397753, rs1573911593, rs1573935244, rs765238394, rs1185619003, rs1573997412, rs775663612, rs958406908, rs754834466, rs749547712, rs1682400034, rs1658967336, rs545032318, rs1695315646, rs1663792524 View all (105 more) |
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Ventricular tachycardia |
Tachycardia, Ventricular |
rs137853228, rs397517025, rs199473373, rs727504432, rs1450434935, rs1592847299 |
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Unknown |
Disease term |
Disease name |
Evidence |
References |
Source |
Long QT Syndrome |
long QT syndrome 16, familial long QT syndrome, long QT syndrome |
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GenCC |
Catecholaminergic Polymorphic Ventricular Tachycardia |
catecholaminergic polymorphic ventricular tachycardia |
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GenCC |
Inflammatory Bowel Disease |
Inflammatory Bowel Disease |
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|
GWAS |
Ulcerative colitis |
Ulcerative colitis |
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|
GWAS |
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Associations from Text Mining |
Disease Name |
Relationship Type |
References |
Alzheimer Disease |
Associate
|
11113632 |
Anthropophobia |
Associate
|
34831335 |
Arrhythmias Cardiac |
Associate
|
23040497, 31170290, 31454269, 32012279, 33211795, 36273583, 37528649 |
Arrhythmogenic Right Ventricular Dysplasia |
Associate
|
27927985, 31454269 |
Atrioventricular Block |
Associate
|
27374306 |
Bradycardia |
Associate
|
27374306 |
Breast Neoplasms |
Associate
|
27129269, 31987794 |
Brugada Syndrome |
Associate
|
19171938 |
Candidiasis Invasive |
Stimulate
|
16603614 |
Carcinoma Hepatocellular |
Associate
|
35724265 |
Channelopathies |
Associate
|
35543671, 37622577 |
Colorectal Neoplasms |
Associate
|
36037145 |
Death |
Associate
|
21546767, 24076290, 26196381, 33200177 |
Death Sudden |
Associate
|
31170290 |
Death Sudden Cardiac |
Associate
|
25036739, 26196381, 27100291, 33200177 |
Electric Injuries |
Associate
|
27100291 |
Fetal Death |
Associate
|
31454269 |
Fractures Malunited |
Associate
|
22009783 |
Fused Teeth |
Associate
|
22009847 |
Glioblastoma |
Associate
|
30816530 |
Glioma |
Associate
|
30816530 |
Heart Arrest |
Associate
|
24917665, 27100291, 27374306, 33200177, 37380439 |
Heart Diseases |
Associate
|
37380439 |
Hemorrhoids |
Associate
|
37932969 |
Hyperaldosteronism |
Associate
|
24403568 |
Inflammatory Bowel Diseases |
Associate
|
19520742 |
Influenza Human |
Associate
|
29059211 |
Intervertebral disc disease |
Associate
|
28583914 |
Leukemia |
Associate
|
37932969 |
Leukemia Myelogenous Chronic BCR ABL Positive |
Associate
|
10681720 |
Long QT Syndrome |
Associate
|
24917665, 26309258, 27374306, 27765793, 31170290, 31454269, 33200177, 35543671, 36273583, 36496072, 37380439 |
Long QT syndrome type 3 |
Associate
|
19265034 |
Lumbar Stenosis Familial |
Associate
|
22009783 |
Melanoma |
Associate
|
1469290 |
Neurofibromatosis Noonan syndrome |
Associate
|
37380439 |
Oculodentodigital Dysplasia |
Associate
|
33080786 |
Osteoarthritis |
Associate
|
18940010, 33563308 |
Paroxysmal ventricular fibrillation |
Associate
|
24076290, 25036739, 31170290, 33200177 |
Polycystic Kidney Autosomal Dominant |
Associate
|
22952279 |
Polymorphic catecholergic ventricular tachycardia |
Associate
|
23040497, 24917665, 26309258, 27100291, 31170290, 32317284, 34557911, 34888671, 37380439 |
Sudden Unexpected Death in Epilepsy |
Associate
|
35543671 |
Syncope |
Associate
|
37380439 |
Tachycardia Ventricular |
Associate
|
32317284, 33200177 |
Thoracic Diseases |
Associate
|
22009783, 22009847 |
Ventricular Fibrillation |
Associate
|
27374306 |
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