LOH19CR1
|
|
loss of heterozygosity, 19, chromosomal region 1
|
|
96
|
0.569 |
0.808 |
|
0.100 |
None
|
1.000 |
10
|
0
|
2012 |
2019 |
CDKN2B-AS1
|
|
CDKN2B antisense RNA 1
|
|
213
|
0.491 |
0.769 |
|
0.020 |
None
|
1.000 |
2
|
5
|
2012 |
2013 |
Entrez Id: |
28 |
Gene Symbol: |
ABO |
ABO
|
P16442
|
ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase
|
Enzyme
|
443
|
0.427 |
0.885 |
|
0.020 |
None
|
1.000 |
2
|
1
|
2014 |
2017 |
P2RX5-TAX1BP3
|
|
P2RX5-TAX1BP3 readthrough (NMD candidate)
|
|
91
|
0.588 |
0.769 |
|
0.010 |
None
|
1.000 |
1
|
0
|
2017 |
2017 |
Entrez Id: |
1038 |
Gene Symbol: |
CDR1 |
CDR1
|
P51861
|
cerebellar degeneration related protein 1
|
|
87
|
0.576 |
0.808 |
|
0.010 |
None
|
1.000 |
1
|
0
|
2019 |
2019 |
LOC107987479
|
|
cytochrome P450 2D6
|
|
76
|
0.597 |
0.769 |
|
0.010 |
None
|
1.000 |
1
|
0
|
2008 |
2008 |
Entrez Id: |
114086 |
Gene Symbol: |
DBA2 |
DBA2
|
|
Diamond-Blackfan anemia 2
|
|
74
|
0.599 |
0.731 |
|
0.010 |
None
|
1.000 |
1
|
0
|
2018 |
2018 |
Entrez Id: |
1218 |
Gene Symbol: |
CMD1B |
CMD1B
|
|
cardiomyopathy, dilated 1B (autosomal dominant)
|
|
20
|
0.722 |
0.500 |
|
0.010 |
None
|
1.000 |
1
|
0
|
2019 |
2019 |
Entrez Id: |
1637 |
Gene Symbol: |
DCR |
DCR
|
|
Down syndrome chromosome region
|
|
32
|
0.674 |
0.538 |
|
0.010 |
None
|
1.000 |
1
|
0
|
2017 |
2017 |
EEF1B2P2
|
|
eukaryotic translation elongation factor 1 beta 2 pseudogene 2
|
|
58
|
0.612 |
0.577 |
|
0.010 |
None
|
1.000 |
1
|
0
|
2013 |
2013 |
Entrez Id: |
263 |
Gene Symbol: |
AMD1P2 |
AMD1P2
|
|
adenosylmethionine decarboxylase 1 pseudogene 2
|
|
71
|
0.608 |
0.538 |
|
0.010 |
None
|
1.000 |
1
|
0
|
2019 |
2019 |
Entrez Id: |
2722 |
Gene Symbol: |
GLC1B |
GLC1B
|
|
glaucoma 1, open angle, B (adult-onset)
|
|
5
|
0.839 |
0.038 |
|
0.010 |
None
|
1.000 |
1
|
0
|
1996 |
1996 |
Entrez Id: |
3439 |
Gene Symbol: |
IFNA1 |
IFNA1
|
P01562
|
interferon alpha 1
|
|
662
|
0.371 |
0.923 |
|
0.010 |
None
|
1.000 |
1
|
0
|
2019 |
2019 |
Entrez Id: |
3440 |
Gene Symbol: |
IFNA2 |
IFNA2
|
P01563
|
interferon alpha 2
|
|
355
|
0.442 |
0.885 |
|
0.010 |
None
|
1.000 |
1
|
0
|
2019 |
2019 |
Entrez Id: |
3447 |
Gene Symbol: |
IFNA13 |
IFNA13
|
P01562
|
interferon alpha 13
|
|
646
|
0.374 |
0.923 |
|
0.010 |
None
|
1.000 |
1
|
0
|
2019 |
2019 |
Entrez Id: |
3456 |
Gene Symbol: |
IFNB1 |
IFNB1
|
P01574
|
interferon beta 1
|
|
426
|
0.421 |
0.846 |
|
0.010 |
None
|
1.000 |
1
|
0
|
2018 |
2018 |
Entrez Id: |
378938 |
Gene Symbol: |
MALAT1 |
MALAT1
|
|
metastasis associated lung adenocarcinoma transcript 1
|
|
336
|
0.435 |
0.846 |
|
0.010 |
None
|
1.000 |
1
|
0
|
2017 |
2017 |
Entrez Id: |
406935 |
Gene Symbol: |
MIR143 |
MIR143
|
|
microRNA 143
|
|
267
|
0.462 |
0.885 |
|
0.010 |
None
|
1.000 |
1
|
0
|
2017 |
2017 |
Entrez Id: |
50968 |
Gene Symbol: |
FCMTE1 |
FCMTE1
|
|
familial cortical myoclonic tremor with epilepsy 1
|
|
12
|
0.769 |
0.231 |
|
0.010 |
None
|
1.000 |
1
|
0
|
2017 |
2017 |
Entrez Id: |
5175 |
Gene Symbol: |
PECAM1 |
PECAM1
|
P16284
|
platelet and endothelial cell adhesion molecule 1
|
Cell adhesion
|
396
|
0.426 |
0.846 |
|
0.010 |
None
|
1.000 |
1
|
0
|
2006 |
2006 |
Entrez Id: |
554188 |
Gene Symbol: |
FCMTE2 |
FCMTE2
|
|
familial cortical myoclonic tremor with epilepsy 2
|
|
14
|
0.743 |
0.231 |
|
0.010 |
None
|
1.000 |
1
|
0
|
2017 |
2017 |
Entrez Id: |
5640 |
Gene Symbol: |
PRS |
PRS
|
|
Prieto X-linked mental retardation syndrome
|
|
42
|
0.663 |
0.615 |
|
0.010 |
None
|
< 0.001 |
1
|
0
|
2019 |
2019 |
Entrez Id: |
653108 |
Gene Symbol: |
CXADRP1 |
CXADRP1
|
|
CXADR pseudogene 1
|
|
272
|
0.463 |
0.846 |
|
0.010 |
None
|
1.000 |
1
|
0
|
2019 |
2019 |
Entrez Id: |
907 |
Gene Symbol: |
CCT |
CCT
|
|
cataract, congenital, total
|
|
75
|
0.588 |
0.769 |
|
0.010 |
None
|
< 0.001 |
1
|
0
|
2018 |
2018 |
Entrez Id: |
9366 |
Gene Symbol: |
RAB9BP1 |
RAB9BP1
|
|
RAB9B, member RAS oncogene family pseudogene 1
|
|
1
|
1.000 |
0.038 |
|
0.010 |
None
|
1.000 |
1
|
0
|
2013 |
2013 |