Entry Detail



General Information

Database ID:exR0361415
RNA Name:CKB
RNA Type:mRNA
Chromosome:chr14
Starnd:-
Coordinate:
Start Site(bp):103519667End Site(bp):103522833
External Links:ENSG00000166165



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
AHNAK
chr11
62433542
62556235
-
AL513165.2
chr9
37512547
37592469
-
AC093525.2
chr16
2496032
2520218
+
AC068580.4
chr11
1734821
1763954
-
AL669918.1
chr6
32813767
32838822
-
AC116366.3
chr5
132410832
132646079
+
ACADVL
chr17
7217125
7225266
+
AHCY
chr20
34280268
34311802
-
AL136295.1
chr14
24189157
24213473
-
AHSA1
chr14
77457870
77469472
+
AATF
chr17
36948954
37056871
+
AC069503.2
chr12
121888809
121921470
+
ADD1
chr4
2843857
2930076
+
ALDH9A1
chr1
165662216
165698863
-
AKAP8L
chr19
15380050
15419141
-
AFF1
chr4
86935002
87141054
+
AL121845.3
chr20
63708864
63739103
+
ACACA
chr17
37084992
37406836
-
AGO2
chr8
140520156
140635633
-
ALDOA
chr16
30064164
30070457
+
ACOT7
chr1
6264269
6394391
-
AC010132.3
chr7
42909273
42932174
-
AC011448.1
chr19
19516227
19536076
+
AIF1L
chr9
131096476
131123152
+
AKR1B1
chr7
134442356
134459284
-
AGAP1
chr2
235494043
236131800
+
AL360181.3
chr10
133380017
133420271
+
ACTB
chr7
5527148
5563784
-
AC010323.1
chr19
8308283
8321379
-
ACTG1
chr17
81509971
81523847
-
miRNA targets:NA
circRNA targets:NA
lncRNA targets:
lncRNA SymbolChromosomeStart Site(bp)End Site(bp)Strand
AC010729.1
chr2
5726253
5730355
+
AC016876.2
chr17
7581964
7584086
-
AC023509.1
chr12
53441741
53467528
+
AC026471.1
chr16
31456711
31459736
-
AC093827.4
chr4
86924630
86936202
-
AC108134.2
chr16
3156736
3157483
-
AL049795.2
chr1
32170733
32176568
+
AL133367.1
chr14
103525010
103529072
-
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.