Entry Detail



General Information

Database ID:exR0359537
RNA Name:AKAP10
RNA Type:mRNA
Chromosome:chr17
Starnd:-
Coordinate:
Start Site(bp):19904302End Site(bp):19978343
External Links:ENSG00000108599



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
TCERG1
chr5
146447311
146511961
+
EFNB2
chr13
106489745
106535662
-
MCFD2
chr2
46901870
46941855
-
ZNF850
chr19
36714383
36772825
-
ATP5MC2
chr12
53632726
53677408
-
PTPRF
chr1
43525187
43623666
+
NSMF
chr9
137447573
137459334
-
GUF1
chr4
44678420
44700928
+
AMPD2
chr1
109616104
109632053
+
MTG2
chr20
62183029
62203568
+
AASDHPPT
chr11
106075501
106098699
+
PROM1
chr4
15963076
16084378
-
RPL27
chr17
42998273
43002959
+
MICALL1
chr22
37905657
37942822
+
ZNF24
chr18
35332227
35345482
-
CSNK1E
chr22
38290691
38318084
-
ICMT
chr1
6221193
6235972
-
ZFAND3
chr6
37819727
38154624
+
SBNO2
chr19
1107637
1174268
-
OGT
chrX
71533104
71575892
+
FOXK2
chr17
82519713
82644662
+
CANX
chr5
179678628
179731641
+
VMP1
chr17
59707192
59842255
+
CREBL2
chr12
12611827
12645108
+
GIGYF2
chr2
232697299
232860575
+
TNFSF9
chr19
6531026
6535924
+
SOBP
chr6
107490106
107661306
+
AP2A2
chr11
924894
1012245
+
SLC35F2
chr11
107790991
107928293
-
AP002990.1
chr11
62559603
62591531
-
miRNA targets:
miRNA SymbolChromosomeStart Site(bp)End Site(bp)Strand
hsa-miR-130a-3p
chr11
57641252
57641273
+
hsa-miR-130b-3p
chr22
21653354
21653375
+
hsa-miR-454-3p
chr17
59137787
59137809
-
circRNA targets:NA
lncRNA targets:
lncRNA SymbolChromosomeStart Site(bp)End Site(bp)Strand
AC079949.1
chr12
127142029
127146532
-
AL645608.1
chr1
1011997
1013193
-
TMEM147-AS1
chr19
35540738
35546029
-
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.