Entry Detail



General Information

Database ID:exR0369140
RNA Name:RPS5
RNA Type:mRNA
Chromosome:chr19
Starnd:+
Coordinate:
Start Site(bp):58386400End Site(bp):58394806
External Links:ENSG00000083845



Disease Information

Disease Name:Amyotrophic Lateral Sclerosis
Disease Category:Nervous System Diseases
MeSH ID:D000690
Type:Diseases Category/Nervous System Diseases
Alias:Sclerosis, Amyotrophic Lateral//Gehrig's Disease//Gehrig Disease//Gehrigs Disease//Charcot Disease//Motor Neuron Disease, Amyotrophic Lateral Sclerosis//Lou Gehrig's Disease//Lou-Gehrigs Disease//Disease, Lou-Gehrigs//ALS - Amyotrophic Lateral Sclerosis//ALS Amyotrophic Lateral Sclerosis//Lou Gehrig Disease//Amyotrophic Lateral Sclerosis, Guam Form//Amyotrophic Lateral Sclerosis-Parkinsonism-Dementia Complex 1//Amyotrophic Lateral Sclerosis Parkinsonism Dementia Complex 1//Guam Form of Amyotrophic Lateral Sclerosis//Guam Disease//Disease, Guam//Amyotrophic Lateral Sclerosis, Parkinsonism-Dementia Complex of Guam//Amyotrophic Lateral Sclerosis, Parkinsonism Dementia Complex of Guam//Amyotrophic Lateral Sclerosis With Dementia//Dementia With Amyotrophic Lateral Sclerosis



Expression Detail

GEO ID:GSE121519
Description:Identification of biomarkers for amyotrophic lateral sclerosis by comprehensive analysis of exosomal mRNAs in human cerebrospinal fluid.
Experimental Design:Disease vs Control
Case Disease Type:Amyotrophic Lateral Sclerosis
Case Disease SubType:NA
Case Sample:Amyotrophic Lateral Sclerosis
Control Sample:Healthy
Number of Case:4
Number of Control:4
Number of Samples:8





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:GSE121519
Sample Source:Cerebrospinal Fluid
Source Fraction:Exosome
Platform:GPL18573
Method:NGS
Num of detected RNA Type:2
Num of detected RNAs of this Type:17787
Sample treatment protocol:Up to 1 mL of human CSF was centrifuged at 2,000×g for 5 min and 10, 000×g for 20 min for supernatant.
RNA Extract protocol:Supernatant from final centrifugation was applied to exoRNeasy spin column and RNA was extracted.
RNA library preparation protocol:Whole cDNA amplification was performed with SMART-seq v4 Ultra Low Input RNA Kit. Illumina library was constructed with Nextera XT DNA Library Prep Kit.



Reference

PMID:30630471
Title:Identification of biomarkers for amyotrophic lateral sclerosis by comprehensive analysis of exosomal mRNAs in human cerebrospinal fluid
Author:Otake K, Kamiguchi H, Hirozane Y
Journal:BMC Med Genomics. 2019 Jan 10;12(1):7.
Description:The main purpose of this study is to established the methodology of comprehensive analysis of exosomal mRNAs in CSF by a highly sensitive next-generation sequencing.