Entry Detail



General Information

Database ID:exR0012329
RNA Name:RPL18A
RNA Type:mRNA
Chromosome:chr19
Starnd:+
Coordinate:
Start Site(bp):17859910End Site(bp):17864153
External Links:ENSG00000105640



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
AL928654.3
chr14
105487199
105492267
+
ALDOA
chr16
30064164
30070457
+
AC073508.2
chr17
40627356
40665141
-
ADGRV1
chr5
90529344
91164437
+
ACAA2
chr18
49782164
49813953
-
AKT1
chr14
104769349
104795751
-
AGPAT5
chr8
6708642
6761503
+
ADD1
chr4
2843857
2930076
+
ABCC10
chr6
43427366
43450427
+
ACTB
chr7
5527148
5563784
-
AC010422.3
chr19
12643831
12648397
-
ABHD5
chr3
43690108
43734371
+
ADAM10
chr15
58588809
58749791
-
ACTN4
chr19
38647649
38731589
+
AASS
chr7
122073549
122144255
-
AGO2
chr8
140520156
140635633
-
AC008982.1
chr19
38817471
38840178
-
ACSF3
chr16
89088375
89164121
+
AHCY
chr20
34280268
34311802
-
ACLY
chr17
41866917
41930542
-
AL359922.1
chr9
21802636
22029594
+
AC104109.3
chr5
134167170
134226071
-
AL358113.1
chr9
69035747
69255187
+
ADAMTS10
chr19
8580240
8610735
-
AC093525.2
chr16
2496032
2520218
+
AC004922.1
chr7
99325879
99394653
+
ABRAXAS2
chr10
124801819
124836667
+
ACADVL
chr17
7217125
7225266
+
AL022318.4
chr22
39014363
39033276
+
AC093525.1
chr16
2513965
2527955
+
miRNA targets:NA
circRNA targets:NA
lncRNA targets:
lncRNA SymbolChromosomeStart Site(bp)End Site(bp)Strand
AC245297.2
chr1
149264252
149264816
+
AD000090.1
chr19
35557956
35581954
+
AL021154.1
chr1
23549139
23550915
-
AL117378.1
chr6
131901963
131920565
+
AL137782.1
chr13
75549773
75807120
+
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.