Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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4645
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Gene name
Gene Name - the full gene name approved by the HGNC.
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Myosin VB |
Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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MYO5B |
Synonyms (NCBI Gene)
Gene synonyms aliases
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DIAR2, MVID1, PFIC10 |
Disease Acronyms (UniProt)
Disease acronyms from UniProt database
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DIAR2, PFIC10 |
Chromosome
Chromosome number
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18 |
Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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18q21.1 |
Summary
Summary of gene provided in NCBI Entrez Gene.
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The protein encoded by this gene, together with other proteins, may be involved in plasma membrane recycling. Mutations in this gene are associated with microvillous inclusion disease. [provided by RefSeq, Sep 2009] |
Causal |
Disease term |
Disease name |
dbSNP ID |
References |
Cholestasis |
Cholestasis |
rs121909103, rs751511532, rs376368459, rs762702807, rs1578490102, rs1578499691, rs1578504946, rs1317656688, rs199791850, rs1452792080, rs1578491039 |
18724368 |
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) |
|
Intrahepatic cholestasis |
Cholestasis, progressive familial intrahepatic 1, MYO5B-related progressive familial intrahepatic cholestasis, Progressive familial intrahepatic cholestasis type 1 |
rs121918299, rs80338722, rs80338725, rs80338719, rs80338723, rs80338726, rs72549401, rs11568372, rs1553469602, rs387907317, rs387906354, rs752919965, rs72549397, rs111033609, rs121909099, rs387906381, rs121909100, rs121909101, rs121909104, rs121909105, rs387906526, rs121918440, rs387906527, rs72552778, rs387906529, rs121918443, rs72552780, rs80338724, rs80338715, rs80338727, rs80338729, rs80338716, rs80338717, rs398122839, rs515726137, rs587777519, rs587777520, rs587777521, rs879255644, rs113090017, rs864321695, rs776869985, rs864321697, rs80338720, rs746155190, rs879255504, rs886041948, rs886042562, rs769910565, rs758069019, rs886043807, rs72549402, rs72549395, rs188824058, rs763782349, rs375315619, rs754287486, rs1057518679, rs1060499649, rs1060499579, rs1554660803, rs1554407511, rs774824767, rs771690686, rs752992432, rs1553466082, rs72549396, rs772294884, rs764513998, rs1202682161, rs759202962, rs1562774655, rs1562831765, rs1562945221, rs917981474, rs1558927163, rs765889649, rs1562976061, rs72549399, rs1459273753, rs377160065, rs1559183717, rs760750012, rs1051861187, rs1558898789, rs928915940, rs752757689, rs1584678508, rs764581483, rs1574453508, rs751511532, rs1182781290, rs376368459, rs762702807, rs1578499691, rs199791850, rs1452792080, rs1458423947, rs1584747270, rs1584750653, rs1599066459, rs1599069873, rs1599166106, rs1574462504, rs1593114820, rs1057524081, rs1588081022, rs777460754, rs1251192873, rs1588117076, rs748671901, rs139314808, rs749009273, rs1588080674, rs1588080680, rs1588127136, rs1588135086, rs757693457, rs1574445178, rs768922690, rs1584422832, rs1584433525, rs1312396424, rs1792048079, rs774411820, rs575729461 View all (111 more) |
27532546 |
Myopia |
Myopia |
rs387907109, rs146936371, rs587776903, rs786205127, rs398122836, rs199624584, rs587777625, rs786205216, rs758872875, rs764211125, rs1135402746, rs765658563, rs1555941129, rs1555941116, rs199923805, rs782555528, rs1554862601, rs1586620121, rs1387950081, rs2051026773, rs1422332023 View all (6 more) |
27182965 |
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) |
23561489 |
|
Unknown |
Disease term |
Disease name |
Evidence |
References |
Source |
Intrahepatic Cholestasis |
progressive familial intrahepatic cholestasis type 1 |
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|
GenCC |
Hypertension |
Hypertension |
|
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GWAS |
Multiple Sclerosis |
Multiple Sclerosis |
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GWAS |
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Associations from Text Mining |
Disease Name |
Relationship Type |
References |
Atrophy |
Associate
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24413175 |
Autoimmune enteropathy |
Associate
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35421597 |
Bipolar Disorder |
Associate
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18317468, 21480485 |
Cholestasis |
Associate
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28027573, 31750554, 35129155, 36705120, 39182182, 40225142 |
Cholestasis Intrahepatic |
Associate
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35129155, 35421597 |
Cholestasis progressive familial intrahepatic 1 |
Associate
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31750554, 39182182 |
Colorectal Neoplasms |
Inhibit
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29024942 |
Cytomegalovirus Infections |
Associate
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34815247 |
Death |
Associate
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27229121 |
Diarrhea |
Associate
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21199752, 21206382, 29218485, 34503561, 35421597 |
Diarrhea 3 Secretory Sodium Congenital |
Associate
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21199752 |
Disease |
Associate
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26823605 |
Dysentery |
Associate
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31596022 |
Dyslexia |
Associate
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24373531 |
Endometrial Neoplasms |
Stimulate
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36662766 |
Epilepsy |
Associate
|
27878761 |
Genetic Diseases Inborn |
Associate
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35421597 |
Glutathionuria |
Associate
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28027573 |
Hypercalciuria Absorptive 1 |
Associate
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26526116 |
Immune Dysregulation Polyendocrinopathy Enteropathy X Linked Syndrome |
Associate
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33864888 |
Insulin Resistance |
Associate
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30678306 |
Intrahepatic Cholestasis of Pregnancy |
Associate
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36705120, 40225142 |
Jaundice |
Associate
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35129155, 39182182 |
Liver Diseases |
Associate
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39182182 |
Malabsorption Syndromes |
Associate
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24413175 |
Microvillus inclusion disease |
Associate
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21199752, 21206382, 23608388, 24138727, 24413175, 24892806, 25258405, 26526116, 26553929, 27229121, 28027573, 29218485, 34503561, 34815247, 35129155, 35421597, 36705120, 37643022, 39182182 View all (4 more) |
Neoplasm Metastasis |
Inhibit
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29024942 |
Neoplasms |
Associate
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32511227, 36522691, 37686244 |
Neuroblastoma |
Associate
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32511227 |
Olfaction Disorders |
Associate
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27878761 |
Pancreatic Neoplasms |
Associate
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36522691 |
Paraganglioma |
Associate
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32511227 |
Pediatric acute onset neuropsychiatric syndrome |
Associate
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27878761 |
Pheochromocytoma |
Associate
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32511227 |
Pruritus |
Associate
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35129155 |
Rare Diseases |
Associate
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35421597 |
Secretory Diarrhea Myopathy and Deafness |
Associate
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24892806 |
Shared Paranoid Disorder |
Associate
|
35421597 |
Stomach Neoplasms |
Associate
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35814566 |
Tooth Loss |
Associate
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27229121 |
Vipoma |
Associate
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28027573 |
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