Entry Detail



General Information

Database ID:exR0000486
RNA Name:ALDH3A2
RNA Type:mRNA
Chromosome:chr17
Starnd:+
Coordinate:
Start Site(bp):19648136End Site(bp):19685760
External Links:ENSG00000072210



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
BLM
chr15
90717346
90816166
+
C4orf3
chr4
119296419
119304445
-
KMT2D
chr12
49018975
49059774
-
EIF5A
chr17
7306999
7312463
+
PRSS16
chr6
27247701
27256624
+
NPM1
chr5
171387116
171411137
+
ERGIC3
chr20
35542021
35557634
+
BST2
chr19
17402939
17405630
-
IQGAP1
chr15
90388242
90502239
+
HMGCR
chr5
75336329
75362101
+
MTRNR2L3
chr20
57358447
57359498
-
PEA15
chr1
160205337
160215376
+
BOD1
chr5
173607145
173616659
-
TUBA1A
chr12
49184795
49189080
-
SPCS1
chr3
52704955
52711148
+
DGLUCY
chr14
91060333
91225632
+
GID8
chr20
62938147
62948475
+
ENSA
chr1
150600851
150629612
-
RSL24D1
chr15
55180806
55197049
-
ARPC2
chr2
218217141
218254356
+
ZNF431
chr19
21142024
21196053
+
MFGE8
chr15
88898683
88913381
-
MIF
chr22
23894383
23895227
+
MPC2
chr1
167916675
167937072
-
TNFRSF14
chr1
2555639
2565382
+
SOX8
chr16
981770
986979
+
PDZD8
chr10
117277274
117375440
-
BCR
chr22
23179704
23318037
+
AK2
chr1
33007940
33080996
-
AMACR
chr5
33986165
34008104
-
miRNA targets:
miRNA SymbolChromosomeStart Site(bp)End Site(bp)Strand
hsa-miR-19b-3p
chr13
91351245
91351267
+
hsa-miR-27a-3p
chr19
13836447
13836467
-
hsa-miR-27b-3p
chr9
95085505
95085525
+
hsa-miR-301a-3p
chr17
59151149
59151171
-
hsa-miR-431-5p
chr14
100881026
100881046
+
circRNA targets:NA
lncRNA targets:
lncRNA SymbolChromosomeStart Site(bp)End Site(bp)Strand
SCARNA9
chr11
93721513
93721865
+
SNHG16
chr17
76557764
76565348
+
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.