Entry Detail



General Information

Database ID:exR0359337
RNA Name:ACTN1
RNA Type:mRNA
Chromosome:chr14
Starnd:-
Coordinate:
Start Site(bp):68874143End Site(bp):68979440
External Links:ENSG00000072110



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
SLCO3A1
chr15
91853708
92172435
+
ATP5F1B
chr12
56638175
56645984
-
MT-CO2
chrMT
7586
8269
+
ZNF865
chr19
55605405
55617269
+
DPM2
chr9
127935099
127938484
-
G3BP1
chr5
151771045
151812785
+
ACTN3
chr11
66546395
66563334
+
VAT1
chr17
43014607
43025123
-
HMGN1
chr21
39342315
39349647
-
SUPT16H
chr14
21351476
21384019
-
PLPP3
chr1
56494761
56645301
-
ERG28
chr14
75649791
75660876
-
PKM
chr15
72199029
72231822
-
SPIN2B
chrX
57118551
57121546
-
NPC2
chr14
74476192
74494177
-
PFKL
chr21
44300051
44327376
+
FYN
chr6
111660332
111873452
-
FARP2
chr2
241356285
241494841
+
TRAF7
chr16
2155698
2178129
+
AC245033.1
chr15
82536788
82573194
-
SEC11A
chr15
84669538
84716460
-
HLA-B
chr6
31269491
31357188
-
DGCR8
chr22
20080232
20111877
+
CHTF8
chr16
69118010
69132578
-
ITFG2
chr12
2812622
2859791
+
POLL
chr10
101578882
101588270
-
POLB
chr8
42338454
42371808
+
ROCK1
chr18
20946906
21111813
-
CNOT1
chr16
58519951
58629885
-
PITPNA
chr17
1517718
1562792
-
miRNA targets:
miRNA SymbolChromosomeStart Site(bp)End Site(bp)Strand
hsa-miR-367-3p
chr4
112647877
112647898
-
circRNA targets:NA
lncRNA targets:
lncRNA SymbolChromosomeStart Site(bp)End Site(bp)Strand
AC245033.4
chr15
82533175
82540008
-
BX284668.5
chr1
16887577
16889706
-
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.