Entrez Id: |
3342 |
Gene Symbol: |
HTC2 |
HTC2
|
|
hypertrichosis 2 (generalized, congenital)
|
|
511
|
0.392 |
0.808 |
|
0.100 |
None
|
1.000 |
60
|
0
|
2003 |
2019 |
Entrez Id: |
2481 |
Gene Symbol: |
FRAXE |
FRAXE
|
|
fragile site, folic acid type, rare, fra(X)(q28) E
|
|
50
|
0.636 |
0.462 |
|
0.100 |
None
|
0.974 |
39
|
0
|
1993 |
2014 |
Entrez Id: |
2477 |
Gene Symbol: |
FRAXA |
FRAXA
|
|
fragile site, folic acid type, rare, fra(X)(q27.3) A (macroorchidism, mental retardation)
|
|
50
|
0.641 |
0.462 |
|
0.100 |
None
|
0.879 |
33
|
0
|
1992 |
2009 |
Entrez Id: |
100528024 |
Gene Symbol: |
DEL11P13 |
DEL11P13
|
|
Wilms tumor, aniridia, genitourinary anomalies and mental retardation syndrome
|
|
24
|
0.716 |
0.538 |
|
0.100 |
None
|
1.000 |
10
|
0
|
1989 |
2011 |
Entrez Id: |
106478973 |
Gene Symbol: |
FMR1-IT1 |
FMR1-IT1
|
|
FMR1 intronic transcript 1
|
|
29
|
0.716 |
0.385 |
|
0.090 |
None
|
1.000 |
9
|
0
|
1992 |
2008 |
Entrez Id: |
406928 |
Gene Symbol: |
MIR137 |
MIR137
|
|
microRNA 137
|
|
171
|
0.513 |
0.846 |
|
0.050 |
None
|
1.000 |
5
|
0
|
2011 |
2018 |
Entrez Id: |
7503 |
Gene Symbol: |
XIST |
XIST
|
|
X inactive specific transcript
|
|
146
|
0.522 |
0.808 |
|
0.040 |
None
|
0.500 |
4
|
0
|
2000 |
2004 |
Entrez Id: |
8422 |
Gene Symbol: |
MEHMO |
MEHMO
|
|
mental retardation, epileptic seizures, hypogonadism and -genitalism, microcephaly and obesity syndrome
|
|
7
|
0.890 |
0.269 |
|
0.040 |
None
|
1.000 |
4
|
0
|
1998 |
2018 |
Entrez Id: |
1637 |
Gene Symbol: |
DCR |
DCR
|
|
Down syndrome chromosome region
|
|
32
|
0.674 |
0.538 |
|
0.030 |
None
|
1.000 |
3
|
0
|
1993 |
1994 |
Entrez Id: |
4412 |
Gene Symbol: |
MRX49 |
MRX49
|
|
mental retardation, X-linked 49
|
|
7
|
0.821 |
0.385 |
|
0.030 |
None
|
1.000 |
3
|
0
|
1999 |
2008 |
Entrez Id: |
7502 |
Gene Symbol: |
XIC |
XIC
|
|
X chromosome inactivation center
|
|
9
|
0.821 |
0.462 |
|
0.030 |
None
|
0.667 |
3
|
0
|
1992 |
1997 |
Entrez Id: |
2448 |
Gene Symbol: |
FRA12A |
FRA12A
|
|
fragile site, folic acid type, rare, fra(12)(q13.1)
|
|
2
|
1.000 |
0.192 |
|
0.020 |
None
|
1.000 |
2
|
0
|
2007 |
2009 |
Entrez Id: |
261 |
Gene Symbol: |
AMCN |
AMCN
|
|
arthrogryposis multiplex congenita, neurogenic
|
|
42
|
0.682 |
0.615 |
|
0.020 |
None
|
1.000 |
2
|
0
|
2019 |
2019 |
Entrez Id: |
100009675 |
Gene Symbol: |
MRT4 |
MRT4
|
|
mental retardation, non-syndromic, autosomal recessive, 4
|
|
1
|
|
|
|
0.010 |
None
|
1.000 |
1
|
0
|
2011 |
2011 |
Entrez Id: |
100038247 |
Gene Symbol: |
PTLS |
PTLS
|
|
Potocki-Lupski syndrome
|
|
17
|
0.780 |
0.308 |
|
0.010 |
None
|
1.000 |
1
|
0
|
2014 |
2014 |
LOC101928437
|
|
uncharacterized LOC101928437
|
|
1
|
|
|
|
0.010 |
None
|
1.000 |
1
|
0
|
2015 |
2015 |
LINC00237
|
|
long intergenic non-protein coding RNA 237
|
|
4
|
0.931 |
0.385 |
|
0.010 |
None
|
1.000 |
1
|
0
|
2012 |
2012 |
RN7SL263P
|
|
RNA, 7SL, cytoplasmic 263, pseudogene
|
|
189
|
0.496 |
0.808 |
|
0.010 |
None
|
1.000 |
1
|
0
|
2019 |
2019 |
Entrez Id: |
115482693 |
Gene Symbol: |
H3P8 |
H3P8
|
|
H3 histone pseudogene 8
|
|
116
|
0.544 |
0.808 |
|
0.010 |
None
|
1.000 |
1
|
0
|
1998 |
1998 |
Entrez Id: |
1218 |
Gene Symbol: |
CMD1B |
CMD1B
|
|
cardiomyopathy, dilated 1B (autosomal dominant)
|
|
20
|
0.722 |
0.500 |
|
0.010 |
None
|
1.000 |
1
|
0
|
2003 |
2003 |
Entrez Id: |
140821 |
Gene Symbol: |
RSS |
RSS
|
|
Russell Silver syndrome
|
|
103
|
0.578 |
0.692 |
|
0.010 |
None
|
1.000 |
1
|
0
|
2017 |
2017 |
DNAJB1P1
|
|
DnaJ heat shock protein family (Hsp40) member B1 pseudogene 1
|
|
51
|
0.650 |
0.654 |
|
0.010 |
None
|
1.000 |
1
|
0
|
2019 |
2019 |
Entrez Id: |
2373 |
Gene Symbol: |
FRA2A |
FRA2A
|
|
fragile site, folic acid type, rare, fra(2)(q11.2)
|
|
1
|
|
|
|
0.010 |
None
|
1.000 |
1
|
0
|
2014 |
2014 |
Entrez Id: |
2667 |
Gene Symbol: |
GDI2P1 |
GDI2P1
|
|
GDP dissociation inhibitor 2 pseudogene 1
|
|
3
|
0.931 |
0.192 |
|
0.010 |
None
|
1.000 |
1
|
0
|
1998 |
1998 |
Entrez Id: |
266790 |
Gene Symbol: |
HCA1 |
HCA1
|
|
Hypercalciuria, absorptive, 1
|
|
50
|
0.633 |
0.654 |
|
0.010 |
None
|
1.000 |
1
|
0
|
2016 |
2016 |