exRNAdisease

Entry Detail

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General Information

Database ID: exR0022451 RNA Name: FTL RNA Type: mRNA Chromosome: chr19 Starnd: + Coordinate: Start Site(bp): 48965309 End Site(bp): 48966879 External Links: ENSG00000087086

Disease Information

Disease Name: Trisomy 18 Syndrome Disease Category: Congenital, Hereditary, and Neonatal Diseases and Abnormalities MeSH ID: D000073842 Type: Diseases Category/Congenital, Hereditary, and Neonatal Diseases and Abnormalities Alias: Trisomy 18 Syndromes//Trisomy E Syndrome//Complete Trisomy 18 Syndrome//Edwards Syndrome//Trisomy 18//Mosaic Trisomy 18 Syndrome

Expression Detail

GEO ID: GSE25634 Description: Expression profiles of amniotic fluid from human fetuses with Trisomy 18 and euploid controls Experimental Design: Disease vs Control Case Disease Type: Trisomy 18 Syndrome Case Disease SubType: NA Case Sample: Trisomy 18 Syndrome Control Sample: Normal Number of Case: 5 Number of Control: 6 Number of Samples: 11

Regulatory Relationship

mRNA targets: Gene Symbol Chromosome Start Site(bp) End Site(bp) Strand AC027644.4 chr7 66628958 66811189 + AC093525.2 chr16 2496032 2520218 + AAGAB chr15 67200667 67255195 - AL136454.1 chr1 192716132 192716653 + AC004922.1 chr7 99325879 99394653 + AGPAT2 chr9 136673143 136687457 - AC018523.2 chr11 14493783 14520344 - AKIRIN2 chr6 87674860 87702233 - AC008763.3 chr19 7678501 7682854 + AK4 chr1 65147549 65232145 + ACLY chr17 41866917 41930542 - AC138969.1 chr16 16317444 16350590 + ADPRH chr3 119579268 119589945 + AC004997.1 chr22 30285238 30299482 - AC069503.2 chr12 121888809 121921470 + AKAP8L chr19 15380050 15419141 - ACTR3 chr2 113890063 113962596 + AC005258.1 chr19 2269525 2341172 + ALDH3A2 chr17 19648136 19685760 + AIP chr11 67483026 67491103 + AIF1L chr9 131096476 131123152 + AIFM2 chr10 70098223 70132934 - ACBD6 chr1 180269653 180502954 - ACTB chr7 5527148 5563784 - ACTR8 chr3 53867066 53882152 - ABHD8 chr19 17292131 17310236 - AC105052.3 chr7 102637049 102671641 - ACP1 chr2 264140 278283 + ADGRA3 chr4 22345071 22516066 - ADD3 chr10 109996368 110135565 + miRNA targets: miRNA Symbol Chromosome Start Site(bp) End Site(bp) Strand hsa-miR-155-5p chr21 25573983 25574006 + hsa-miR-639 chr19 14529603 14529625 + hsa-miR-4426 chr1 192716333 192716349 + circRNA targets: NA lncRNA targets: lncRNA Symbol Chromosome Start Site(bp) End Site(bp) Strand AC002467.1 chr7 107739999 107744581 - AC004687.1 chr17 58330884 58332508 - AC005696.1 chr17 2712309 2712833 + AC006504.5 chr19 27793431 27984984 + AC007114.1 chr17 57071814 57085024 - AC007952.4 chr17 19112000 19112636 - AC009908.1 chr8 124996985 124998198 - AC010327.5 chr19 55216660 55221616 + AC016876.2 chr17 7581964 7584086 - AC021078.1 chr5 149494314 149504670 - AC026362.1 chr12 122975320 122982907 + AC079174.2 chr12 106250759 106252786 + AC118553.1 chr1 99968383 99969864 - AD000090.1 chr19 35557956 35581954 + AL022157.1 chrX 57121662 57127243 + AL022311.1 chr22 37876148 37895563 + AL033527.3 chr1 39788976 39790171 + AL137230.2 chr14 89628921 89642671 - Display:

Experiment Detail

GEO ID: GSE25634 Sample Source: Amniotic Fluid Source Fraction: Supernatant Platform: GPL570 Method: Microarray Num of detected RNA Type: 1 Num of detected RNAs of this Type: 17063 Sample treatment protocol: NA RNA Extract protocol: RNA was extracted from 10 mL amniotic fluid supernatant with 30 mL TRIzol LS Reagent (Invitrogen, Carlsbad, CA) and 8 mL chloroform. RNA library preparation protocol: biotin Samples were labeled using the FL-Ovation™ cDNA Biotin Module V2 (NuGEN, San Carlos, CA).

Reference

PMID: NA Title: NA Author: NA Journal: NA Description: NA