Entry Detail



General Information

Database ID:exR0359259
RNA Name:ABL2
RNA Type:mRNA
Chromosome:chr1
Starnd:-
Coordinate:
Start Site(bp):179099330End Site(bp):179229684
External Links:ENSG00000143322



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
FBXL19
chr16
30923055
30948783
+
AC010422.3
chr19
12643831
12648397
-
SRPK2
chr7
105110704
105399308
-
KIAA0753
chr17
6578147
6640711
-
WDR74
chr11
62832342
62841809
-
RPL11
chr1
23691742
23696835
+
DNAH1
chr3
52316319
52400491
+
APBB3
chr5
140558268
140564781
-
HECTD4
chr12
112160188
112382439
-
RPS3
chr11
75399515
75422280
+
ARPP19
chr15
52547045
52569883
-
INPPL1
chr11
72223701
72239147
+
LRWD1
chr7
102464956
102473168
+
KPNA5
chr6
116681187
116741867
+
RPL12
chr9
127447674
127451406
-
KMT2D
chr12
49018975
49059774
-
UGDH
chr4
39498755
39528311
-
ZC4H2
chrX
64915802
65034713
-
PTMA
chr2
231706895
231713541
+
PDPN
chr1
13583465
13617957
+
CHCHD10
chr22
23765834
23768443
-
FUCA2
chr6
143494812
143511720
-
TEAD3
chr6
35473597
35497079
-
HNRNPM
chr19
8444767
8489114
+
ABL1
chr9
130713016
130887675
+
GLUL
chr1
182381704
182392206
-
UBR4
chr1
19074510
19210266
-
SSR2
chr1
156009048
156020951
-
RPL13A
chr19
49487554
49492308
+
IMP4
chr2
130342877
130347967
+
miRNA targets:
miRNA SymbolChromosomeStart Site(bp)End Site(bp)Strand
hsa-miR-154-5p
chr14
101059769
101059790
+
hsa-miR-188-5p
chrX
50003517
50003537
+
hsa-miR-339-5p
chr7
1022990
1023012
-
hsa-miR-625-5p
chr14
65471116
65471136
+
hsa-miR-425-5p
chr3
49020199
49020221
-
hsa-miR-532-3p
chrX
50003204
50003225
+
hsa-miR-1224-5p
chr3
184241405
184241423
+
circRNA targets:NA
lncRNA targets:
lncRNA SymbolChromosomeStart Site(bp)End Site(bp)Strand
HIPK1-AS1
chr1
113924000
113929495
-
XIST
chrX
73820649
73852723
-
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.