Entry Detail



General Information

Database ID:exR0006577
RNA Name:HSP90AB1
RNA Type:mRNA
Chromosome:chr6
Starnd:+
Coordinate:
Start Site(bp):44246166End Site(bp):44253888
External Links:ENSG00000096384



Disease Information

Disease Name:Down Syndrome
Disease Category:Congenital, Hereditary, and Neonatal Diseases and Abnormalities
MeSH ID:D004314
Type:Diseases Category/Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Alias:Syndrome, Down//Mongolism//47,XY,+21//Trisomy G//47,XX,+21//Down's Syndrome//Downs Syndrome//Syndrome, Down's//Trisomy 21//Trisomy 21, Mitotic Nondisjunction//Down Syndrome, Partial Trisomy 21//Partial Trisomy 21 Down Syndrome//Trisomy 21, Meiotic Nondisjunction



Expression Detail

GEO ID:GSE16176
Description:Expression profiles of amniotic fluid from human fetuses with Down syndrome and euploid controls
Experimental Design:Disease vs Control
Case Disease Type:Down Syndrome
Case Disease SubType:NA
Case Sample:Down Syndrome
Control Sample:Normal
Number of Case:7
Number of Control:7
Number of Samples:14





Regulatory Relationship

mRNA targets:
Gene SymbolChromosomeStart Site(bp)End Site(bp)Strand
AGBL5
chr2
27042364
27070622
+
ADAM10
chr15
58588809
58749791
-
AC022384.1
chr3
10249372
10285796
+
AC008982.1
chr19
38817471
38840178
-
AKIRIN2
chr6
87674860
87702233
-
AHCYL2
chr7
129225023
129430211
+
AC068946.1
chr2
219075329
219170827
-
AC007192.1
chr19
18153158
18178117
+
ALDH4A1
chr1
18871430
18902724
-
AKAP1
chr17
57085092
57121346
+
ALDOA
chr16
30064164
30070457
+
AC135050.2
chr16
31083439
31094956
-
ABCB6
chr2
219209772
219218994
-
AGPAT5
chr8
6708642
6761503
+
ABHD14A-ACY1
chr3
51974706
51989183
+
ADPRM
chr17
10697594
10711558
+
AK4
chr1
65147549
65232145
+
ABRACL
chr6
139028745
139043302
+
AGO3
chr1
35930718
36072500
+
ACIN1
chr14
23058564
23095614
-
AC005726.1
chr17
28455752
28614185
-
AL358075.4
chr1
46043661
46176488
-
AKT1
chr14
104769349
104795751
-
ADCY2
chr5
7396138
7830081
+
AKR1B1
chr7
134442356
134459284
-
ABL1
chr9
130713016
130887675
+
AJAP1
chr1
4654609
4792534
+
ADAM23
chr2
206443532
206621127
+
AARS2
chr6
44298731
44313347
-
AKAP8L
chr19
15380050
15419141
-
miRNA targets:
miRNA SymbolChromosomeStart Site(bp)End Site(bp)Strand
hsa-miR-320a-3p
chr8
22244975
22244996
-
hsa-miR-485-5p
chr14
101055427
101055448
+
hsa-miR-4485-3p
chr11
10508277
10508296
-
circRNA targets:NA
lncRNA targets:
lncRNA SymbolChromosomeStart Site(bp)End Site(bp)Strand
AC009133.5
chr16
29808679
29812227
+
AC010642.2
chr19
58309727
58327248
-
AC016026.1
chr22
17787652
17811497
-
AC016876.2
chr17
7581964
7584086
-
AC021078.1
chr5
149494314
149504670
-
AC023509.1
chr12
53441741
53467528
+
AC024940.6
chr12
31280422
31280895
-
AC026362.1
chr12
122975320
122982907
+
AC026464.2
chr16
69463844
69466264
+
AC064802.1
chr8
114282067
114295839
+
AC079781.5
chr7
97851688
97972985
-
AC091820.1
chr5
167296234
167303372
-
AC092143.3
chr16
89906157
89918233
+
AC097478.1
chr4
89743792
89744305
+
AC104109.2
chr5
134226410
134227827
+
AC109460.3
chr16
28974804
28990775
+
AC132217.1
chr11
2129121
2129964
-
AC245014.3
chr1
145281116
145281462
+
AD000090.1
chr19
35557956
35581954
+
AL022311.1
chr22
37876148
37895563
+
AL121749.1
chr10
35604485
35608153
-
Display:



Experiment Detail

GEO ID:GSE16176
Sample Source:Amniotic Fluid
Source Fraction:Supernatant
Platform:GPL570
Method:Microarray
Num of detected RNA Type:1
Num of detected RNAs of this Type:17063
Sample treatment protocol:NA
RNA Extract protocol:RNA was extracted from 10 mL AF with 30 mL TRIzol LS Reagent (Invitrogen, Carlsbad, CA) and 8 mL chloroform. After RNA extraction, RNA was purified and DNA was removed using the RNeasy® Maxi Kit, including the DNase step according to the manufacturer's protocol (QIAGEN, Valencia, CA). RNA was precipitated using 3M NaOAc and 100% ethanol, and 80% ethanol was added after 4 hours incubation at -20 °C. cDNA, synthesized from extracted RNA, was amplified and purified using the WT-Ovation™ Pico RNA Amplification System (NuGEN, San Carlos, CA) and the DNA Clean & Concentrator™-25 (Zymo Research, Orange, CA).
RNA library preparation protocol:biotin Samples were labeled using the FL-Ovation™ cDNA Biotin Module V2 (NuGEN, San Carlos, CA).



Reference

PMID:19474297
Title:Functional genomic analysis of amniotic fluid cell-free mRNA suggests that oxidative stress is significant in Down syndrome fetuses
Author:Slonim DK, Koide K, Johnson KL, Tantravahi U, Cowan JM, Jarrah Z, Bianchi DW
Journal:Proc Natl Acad Sci U S A. 2009 Jun 9;106(23):9425-9.
Description:To characterize the differences between second trimester Down syndrome (DS) and euploid fetuses, we used Affymetrix microarrays to compare gene expression in uncultured amniotic fluid supernatant samples.