Entry Detail



General Information

Database ID:exR0006399
RNA Name:HMGA1
RNA Type:mRNA
Chromosome:chr6
Starnd:+
Coordinate:
Start Site(bp):34236873End Site(bp):34246231
External Links:ENSG00000137309



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
ACTR2
chr2
65227753
65271253
+
ADNP
chr20
50888916
50931437
-
AKR7A2
chr1
19303965
19312146
-
ADH5
chr4
99070978
99088801
-
ADM
chr11
10305073
10307397
+
AC008982.1
chr19
38817471
38840178
-
ADGRL1
chr19
14147743
14206187
-
AGPAT1
chr6
32168212
32178096
-
ADGRA3
chr4
22345071
22516066
-
AGFG2
chr7
100539203
100568220
+
ACLY
chr17
41866917
41930542
-
AJUBA
chr14
22971177
22982551
-
AK4
chr1
65147549
65232145
+
AAMP
chr2
218264123
218270257
-
AC009133.6
chr16
29812261
29820092
+
AHCYL2
chr7
129225023
129430211
+
AC068547.1
chr2
151802651
151973949
-
AC015813.2
chr17
57989038
58007246
-
AKAP13
chr15
85380571
85749358
+
AFTPH
chr2
64524305
64593005
+
AK5
chr1
77282019
77559966
+
ADRM1
chr20
62302093
62308862
+
ACER3
chr11
76860867
77026797
+
AL121594.1
chr14
35122549
35317474
+
ACTA1
chr1
229431245
229434098
-
AHCY
chr20
34280268
34311802
-
ABRACL
chr6
139028745
139043302
+
ADARB1
chr21
45073853
45226560
+
AL136454.1
chr1
192716132
192716653
+
ACAD10
chr12
111686056
111757107
+
miRNA targets:
miRNA SymbolChromosomeStart Site(bp)End Site(bp)Strand
hsa-let-7a-5p
chr9
94175962
94175983
+
hsa-let-7d-5p
chr9
94178841
94178862
+
hsa-let-7e-5p
chr19
51692793
51692814
+
hsa-miR-21-5p
chr17
59841273
59841294
+
hsa-miR-138-5p
chr16
56858527
56858549
+
hsa-miR-423-5p
chr17
30117095
30117117
+
hsa-miR-1321
chrX
85835832
85835849
+
hsa-miR-3654
chr7
133034860
133034878
-
hsa-miR-6835-3p
chr6
34240714
34240736
+
circRNA targets:NA
lncRNA targets:
lncRNA SymbolChromosomeStart Site(bp)End Site(bp)Strand
AC007952.4
chr17
19112000
19112636
-
AC010331.1
chr19
47607873
47608454
-
AC016876.2
chr17
7581964
7584086
-
AC019205.1
chr6
73263212
73301789
+
AC020663.1
chr16
4730115
4752565
-
AC020928.2
chr19
36773712
36775908
-
AC025271.4
chr15
57553955
57555680
+
AC079781.5
chr7
97851688
97972985
-
AC104971.1
chr18
58670009
58671877
-
AC126365.1
chr17
20788071
20789584
+
AC132217.1
chr11
2129121
2129964
-
AD000090.1
chr19
35557956
35581954
+
AL022311.1
chr22
37876148
37895563
+
AL117378.1
chr6
131901963
131920565
+
AL132780.1
chr14
22929607
22956374
+
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.