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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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1006
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Gene name
Gene Name - the full gene name approved by the HGNC.
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Cadherin 8 |
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Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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CDH8 |
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Synonyms (NCBI Gene)
Gene synonyms aliases
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Nbla04261 |
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Chromosome
Chromosome number
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16 |
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Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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16q21 |
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Summary
Summary of gene provided in NCBI Entrez Gene.
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This gene encodes a type II classical cadherin from the cadherin superfamily, integral membrane proteins that mediate calcium-dependent cell-cell adhesion. Mature cadherin proteins are composed of a large N-terminal extracellular domain, a single membrane |
| Causal |
| Disease term |
Disease name |
dbSNP ID |
References |
| Parkinson disease |
Parkinson Disease |
rs33939927, rs35801418, rs34805604, rs35870237, rs34995376, rs74315355, rs28940284, rs74315356, rs74315357, rs28940285, rs730880302, rs750664040, rs74315359, rs74315360, rs45539432, rs119451946, rs80356771, rs74500255, rs75822236, rs1141814, rs78973108, rs121908681, rs121908686, rs121908687, rs137853054, rs137853055, rs137853056, rs137853057, rs137853058, rs137853059, rs34424986, rs137853060, rs397518439, rs28938172, rs74315351, rs74315353, rs137853051, rs118192098, rs121918104, rs1589451049, rs104893877, rs104893878, rs188286943, rs387906863, rs387906864, rs774631197, rs199935023, rs397514694, rs398122403, rs398122404, rs398122405, rs104886460, rs409652, rs431905511, rs63751392, rs756677845, rs864309527, rs864309650, rs750014782, rs1554391082, rs864622011, rs869312810, rs869312809, rs869312811, rs369100678, rs879253853, rs869320761, rs747506979, rs879255630, rs886039854, rs191486604, rs781442277, rs1060499619, rs751037529, rs55777503, rs768091663, rs34208370, rs1553122929, rs772786691, rs754809877, rs1555907463, rs1557561340, rs781600849, rs141263564, rs1557901552, rs777160388, rs756783990, rs867929413, rs1237637353, rs1005937012, rs755000580, rs747427602, rs1578089802, rs771586218, rs748142049, rs1582953433, rs746646126, rs771529549, rs121918106 View all (84 more) |
21812969 |
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| Unknown |
| Disease term |
Disease name |
Evidence |
References |
Source |
| Mental depression |
Major Depressive Disorder |
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27622933 |
ClinVar |
| Breast Cancer |
Breast Cancer |
Importantly, breast cancer patients bearing PRC2 LOF mutations displayed significantly worse prognosis compared with PRC2 wild-type patients |
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GWAS, CBGDA |
| Insomnia |
Insomnia |
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GWAS |
| Oligodendroglioma |
Oligodendroglioma |
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GWAS |
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| Associations from Text Mining |
| Disease Name |
Relationship Type |
References |
| Autism Spectrum Disorder |
Associate
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23879678 |
| Autistic Disorder |
Associate
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20972252, 23575222 |
| Carcinoma Squamous Cell |
Associate
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28177435 |
| Cysts |
Associate
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21389276 |
| Learning Disabilities |
Associate
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20972252 |
| Neoplasms |
Inhibit
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27651839 |
| Pemphigus |
Associate
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23505434 |
| Polycystic Kidney Autosomal Dominant |
Associate
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21389276 |
| Pterygium |
Associate
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40033254 |
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