Entry Detail



General Information

Database ID:exR0012414
RNA Name:RPS5
RNA Type:mRNA
Chromosome:chr19
Starnd:+
Coordinate:
Start Site(bp):58386400End Site(bp):58394806
External Links:ENSG00000083845



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
AGFG2
chr7
100539203
100568220
+
AL358113.1
chr9
69035747
69255187
+
AKAP1
chr17
57085092
57121346
+
ACO2
chr22
41469117
41528989
+
AL022238.4
chr22
40346529
40410054
+
AC004832.3
chr22
30409255
30428990
+
AC007192.1
chr19
18153158
18178117
+
AC139530.2
chr17
81703371
81720539
+
AC010422.3
chr19
12643831
12648397
-
AC092073.1
chr19
34396315
34409364
+
AC040162.1
chr16
67929614
67936017
-
ABRACL
chr6
139028745
139043302
+
ACTN4
chr19
38647649
38731589
+
AHDC1
chr1
27534035
27604431
-
AHCYL1
chr1
109984765
110023742
+
AHCY
chr20
34280268
34311802
-
ACTR1B
chr2
97655939
97664044
-
ACTB
chr7
5527148
5563784
-
ALDOA
chr16
30064164
30070457
+
AK2
chr1
33007940
33080996
-
AC008763.3
chr19
7678501
7682854
+
AC002985.1
chr19
18907013
18934397
-
AC011462.1
chr19
41350853
41425001
+
ABHD10
chr3
111979010
111993368
+
AC018523.2
chr11
14493783
14520344
-
AC104452.1
chr3
49416777
49429314
-
AHSA1
chr14
77457870
77469472
+
ABCC1
chr16
15949577
16143074
+
ADSL
chr22
40346500
40390463
+
AACS
chr12
125065434
125143333
+
miRNA targets:
miRNA SymbolChromosomeStart Site(bp)End Site(bp)Strand
hsa-miR-1244
chr2
231713368
231713393
+
circRNA targets:NA
lncRNA targets:
lncRNA SymbolChromosomeStart Site(bp)End Site(bp)Strand
AC026362.1
chr12
122975320
122982907
+
AC091564.7
chr11
6610883
6616594
-
AC121761.1
chr12
75483454
75489820
-
AD000090.1
chr19
35557956
35581954
+
AL121832.3
chr20
62402236
62405935
-
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.