Entry Detail



General Information

Database ID:exR0359297
RNA Name:ACIN1
RNA Type:mRNA
Chromosome:chr14
Starnd:-
Coordinate:
Start Site(bp):23058564End Site(bp):23095614
External Links:ENSG00000100813



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
HNRNPA2B1
chr7
26173057
26201529
-
CD74
chr5
150400041
150412929
-
EEF1G
chr11
62559596
62574086
-
MANEAL
chr1
37793802
37801137
+
CGN
chr1
151510510
151538692
+
LRRC58
chr3
120324509
120349354
-
RGPD5
chr2
109792758
109857705
+
IVNS1ABP
chr1
185296388
185317273
-
TTLL3
chr3
9808086
9855138
+
SDHAF3
chr7
97117698
97181763
+
JAGN1
chr3
9890574
9894349
+
RPL39
chrX
119786504
119791630
-
CFAP20
chr16
58113592
58129381
-
PCDHGA3
chr5
141343829
141512979
+
PCDHGA1
chr5
141330571
141512981
+
ALDH7A1
chr5
126531200
126595362
-
EEF1A1
chr6
73515750
73523797
-
PMF1
chr1
156212993
156240042
+
WWC3
chrX
10015562
10144478
+
RACK1
chr5
181236897
181248096
-
SFXN1
chr5
175477062
175529742
+
TPT1
chr13
45333471
45341370
-
MRPS7
chr17
75261674
75266376
+
RNASEK
chr17
7012417
7014532
+
TRAF7
chr16
2155698
2178129
+
CERK
chr22
46684410
46738252
-
TSC2
chr16
2047967
2089491
+
CNP
chr17
41966763
41977740
+
RPL11
chr1
23691742
23696835
+
PCDHGA10
chr5
141412987
141512979
+
miRNA targets:NA
circRNA targets:NA
lncRNA targets:
lncRNA SymbolChromosomeStart Site(bp)End Site(bp)Strand
AC027682.2
chr16
67542123
67542963
-
AC124068.2
chr15
89335053
89336161
+
AL132780.1
chr14
22929607
22956374
+
AL355075.4
chr14
20343048
20343685
-
AP001496.2
chr18
5232876
5238526
-
AP005263.1
chr18
9102736
9254346
+
BISPR
chr19
17405686
17419324
+
NEAT1
chr11
65422774
65445540
+
XIST
chrX
73820649
73852723
-
Z83843.1
chrX
74209976
74213660
-
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.