Entry Detail



General Information

Database ID:exR0359274
RNA Name:ACAD10
RNA Type:mRNA
Chromosome:chr12
Starnd:+
Coordinate:
Start Site(bp):111686056End Site(bp):111757107
External Links:ENSG00000111271



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
NDUFA10
chr2
239892450
240025345
-
GPCPD1
chr20
5544439
5611006
-
IPP
chr1
45694324
45750653
-
MRM2
chr7
2234195
2242205
-
SLAMF6
chr1
160485030
160523262
-
MYH9
chr22
36281277
36388067
-
SLC52A2
chr8
144354135
144361272
+
CPT1C
chr19
49690898
49713731
+
PSMD11
chr17
32444379
32483319
+
HMGB2
chr4
173331376
173334432
-
SP110
chr2
230167293
230225729
-
CBX3
chr7
26201162
26213607
+
DNAJC25
chr9
111631334
111654351
+
PTP4A3
chr8
141391995
141432454
+
CMTR1
chr6
37433219
37482827
+
PLXNA1
chr3
126988594
127037392
+
ZBED4
chr22
49853844
49890080
+
ST8SIA1
chr12
22063773
22437041
-
ACTN1
chr14
68874143
68979440
-
UBE2Z
chr17
48908407
48929056
+
GRK2
chr11
67266473
67286556
+
DCTN2
chr12
57530102
57547331
-
FOXM1
chr12
2857681
2877155
-
MT-ND1
chrMT
3307
4262
+
VIPAS39
chr14
77426675
77457952
-
EPM2AIP1
chr3
36985043
36993131
-
ST6GAL1
chr3
186930502
187078553
+
TPGS2
chr18
36777647
36829216
-
AL132780.3
chr14
22946270
22982258
-
FSCN3
chr7
127591409
127602144
+
miRNA targets:NA
circRNA targets:NA
lncRNA targets:NA
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.