Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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5332
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Gene name
Gene Name - the full gene name approved by the HGNC.
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Phospholipase C beta 4 |
Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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PLCB4 |
Synonyms (NCBI Gene)
Gene synonyms aliases
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ARCND2, ARCND2A, ARCND2B, PI-PLC |
Disease Acronyms (UniProt)
Disease acronyms from UniProt database
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ARCND2A, ARCND2B |
Chromosome
Chromosome number
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20 |
Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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20p12.3-p12.2 |
Summary
Summary of gene provided in NCBI Entrez Gene.
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The protein encoded by this gene catalyzes the formation of inositol 1,4,5-trisphosphate and diacylglycerol from phosphatidylinositol 4,5-bisphosphate. This reaction uses calcium as a cofactor and plays an important role in the intracellular transduction |
Causal |
Disease term |
Disease name |
dbSNP ID |
References |
Auriculocondylar syndrome |
Auriculo-condylar syndrome, AURICULOCONDYLAR SYNDROME 2, Auriculocondylar syndrome 1, Auriculocondylar syndrome |
rs387907178, rs397514480, rs387907179, rs397514481, rs397514482, rs397514483, rs397514768, rs397514769, rs397514770, rs397514771, rs587777231, rs587777232, rs1553223897 |
22560091, 23315542 |
Developmental delay |
Global developmental delay |
rs28941770, rs199469464, rs281865469, rs143747297, rs398123009, rs587777428, rs786205133, rs606231459, rs797044854, rs797045027, rs864309504, rs878853160, rs886039902, rs886042046, rs886041291, rs886041382, rs1057518991, rs1057518699, rs753254213, rs748294403, rs762552974, rs1135401795, rs1553121073, rs1553122926, rs1364690005, rs1554086554, rs1554210415, rs1554168326, rs1554776342, rs1553873247, rs1567860112, rs779009256, rs1557447255, rs1564568350, rs780011005, rs1597464953, rs1200336864, rs1569513017, rs1587459606, rs1570332505, rs748888652, rs1575155995, rs2087029320, rs1589669105, rs1601769604, rs1184981709, rs749201074 View all (32 more) |
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Macrocephaly |
Macrocephaly |
rs786204854, rs764333096, rs1557739557 |
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Melanoma |
melanoma |
rs121913315, rs121913323, rs137853080, rs137853081, rs121909232, rs121913388, rs104894094, rs104894095, rs104894097, rs104894098, rs104894099, rs104894109, rs137854599, rs11547328, rs104894340, rs398123152, rs587780668, rs587782083, rs587782206, rs587782792, rs180177042, rs121913381, rs730881675, rs730881674, rs730881677, rs730881673, rs1800586, rs768966657, rs587778189, rs786204195, rs121913321, rs45476696, rs864622636, rs864622263, rs869025340, rs876660436, rs876658534, rs876658556, rs878853647, rs878853644, rs878853650, rs886041162, rs121913389, rs1057519852, rs121913384, rs121913387, rs1060501266, rs1060501263, rs1060501262, rs749714198, rs1060501265, rs559848002, rs1064794292, rs1131691187, rs1131691186, rs199907548, rs1554654052, rs1554656411, rs1554656624, rs1554653915, rs1554653956, rs1554656253, rs1554654224, rs754806883, rs1057520039, rs1563889584, rs1563889685, rs1287464120, rs1563888944, rs1563892715, rs1563889847, rs141798398, rs1587332338, rs1587340291, rs11552823, rs561034503, rs138677674, rs1819962958, rs1820531050 View all (64 more) |
21499247 |
Multiple congenital anomalies |
Multiple congenital anomalies |
rs1057517732 |
18314001, 27007857, 23315542, 28328130, 22560091, 16114046 |
Schizophrenia |
Schizophrenia |
rs13447324, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346, rs863223347, rs863223351, rs863223352, rs61734270, rs797045205, rs869312829, rs869312830, rs770913157, rs869312832, rs869312831, rs781720548, rs1262969313 View all (12 more) |
29064472 |
Uveal melanoma |
Uveal melanoma |
rs1559588632 |
27089179 |
|
Unknown |
Disease term |
Disease name |
Evidence |
References |
Source |
Ptosis |
Blepharoptosis, Ptosis |
|
|
ClinVar |
Vein of galen aneurysm |
Vein of Galen aneurysm |
|
|
ClinVar |
Auriculocondylar Syndrome |
auriculocondylar syndrome |
|
|
GenCC |
Metabolic Syndrome |
Metabolic Syndrome |
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|
GWAS |
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Associations from Text Mining |
Disease Name |
Relationship Type |
References |
Adenocarcinoma |
Associate
|
31080817 |
Adenoma Islet Cell |
Associate
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30575306 |
Auriculo condylar syndrome |
Associate
|
22560091, 24268655, 30806792 |
Bone Diseases Developmental |
Associate
|
29122926 |
Breast Neoplasms |
Associate
|
29512753 |
Carcinogenesis |
Associate
|
34905385 |
Carcinoma Hepatocellular |
Associate
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30896816 |
Carcinoma Non Small Cell Lung |
Associate
|
31080817 |
Carcinoma Pancreatic Ductal |
Associate
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35255936 |
Colonic Neoplasms |
Associate
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32420374 |
Colorectal Neoplasms |
Associate
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31729423, 36927770 |
Coronary Aneurysm |
Associate
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26434682 |
Down Syndrome |
Associate
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27293319 |
Endometrial Neoplasms |
Associate
|
22706224 |
Eye Abnormalities |
Associate
|
29122926 |
Gastrointestinal Stromal Tumors |
Associate
|
28212550 |
Hemangioblastoma |
Associate
|
28742274 |
Inflammation |
Associate
|
26434682, 28880852 |
Melanoma |
Associate
|
34905385 |
Mental Disorders |
Associate
|
21494683 |
Metabolic Syndrome |
Associate
|
21494683 |
Mucocutaneous Lymph Node Syndrome |
Associate
|
26434682 |
Mucopolysaccharidoses |
Associate
|
32886284 |
Neoplasms |
Associate
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28212550, 30896816, 31186267, 31729423, 32415113 |
Nevus Blue |
Associate
|
27934878, 28409567 |
Optic Disk Drusen |
Associate
|
39865650 |
Osteoporosis |
Associate
|
34899595 |
Pancreatitis |
Associate
|
21494683 |
Precursor T Cell Lymphoblastic Leukemia Lymphoma |
Associate
|
30575306 |
Prurigo |
Associate
|
37245863 |
Schwartz Cohen Addad Lambert syndrome |
Associate
|
31186267 |
Sleep Initiation and Maintenance Disorders |
Associate
|
21494683 |
Tuberculosis Multidrug Resistant |
Associate
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29512753 |
Uveal melanoma |
Associate
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26683228, 27934878, 29726589, 31186267, 32415113, 33348918, 34905385 |
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