HsaINT0152366 @ hg19
Intron Retention
Gene
ENSG00000136856 | SLC2A8
Description
solute carrier family 2 (facilitated glucose transporter), member 8 [Source:HGNC Symbol;Acc:13812]
Coordinates
chr9:130160184-130162285:+
Coord C1 exon
chr9:130160184-130160390
Coord A exon
chr9:130160391-130162185
Coord C2 exon
chr9:130162186-130162285
Length
1795 bp
Sequences
Splice sites
5' ss Seq
CCGGTGAGT
5' ss Score
10.9
3' ss Seq
CCTCATCTGATTGCTGGCAGGTC
3' ss Score
7.14
Exon sequences
Seq C1 exon
GCTGTCGTGACCCTGGGTGCCGCGGCGGGGGGAGTGCTGGGCGGCTGGCTGGTGGACCGCGCCGGGCGCAAGCTGAGCCTCTTGCTGTGCTCCGTGCCCTTCGTGGCCGGCTTTGCCGTCATCACCGCGGCCCAGGACGTGTGGATGCTGCTGGGGGGCCGCCTCCTCACCGGCCTGGCCTGCGGTGTTGCCTCCCTAGTGGCCCCG
Seq A exon
GTGAGTGTCCCGTCTCTCGAGTGTCCTGTCTCGCGGCCTGAGACCGAGGGGGAGTGGGACAAACCGCTCCCCAGGCCTGGGGGCGCGGCTCCCCCTGGCGGGACCTTCTGGGTGCCAGGCTTGAAGTCCCTGCGTTATCTCGCGGTCCCTCCCGTCGACCCTGGGAAGGATCCTACTGTTCTCTCCATTTTACACTGAGGTCATGACATGCAGTCTCGGAAAGGTGAAGTCCTTTGCCCAGGCGAGGTCCACAGCTAGTCAGAGGGGAAGCAGTTGCAGGAACCCAGGGTTGTCCCACTTAGCCGTGCCCCTCTTTTGCTCTGCAAACCTGCGGATGATCCACAGGAGCCCACTCCCTACATTTTGGTTTTCATCCCTGGCTTCGGGTCAATGACTGCAATTAGCAGGAAGTTCCTGTCCTGATTTCTCTTGGGGCAAAGGCTGCTGGCCTCTGTGTTCCCCTTCCCTTCTCACAGGCCAGCCCCTCTGGCTTCCCCATCTTCCCCCTTTCCCCCTCCTGACCCAGGCTGCCCACTTGGGAGCCCCGAACATCTGGGTCAAATCCTGGTTCTGCCACTAACCTGAGCAGAGTGCCTCCCTGGGCCTCAGTTTCCTTCTCTGGAAAACAGGGATTATGGCATTAGCCCCTGAGGTAGTGGTCAGGATTCAGTGGGACTTTGGATAGACAGCCCCTGGCATGGCTTGTAGAGGACTGGATCCTGACAGCTTGGTGACCCATGAACTGCCCCCAGCCATGGGCTTGGACAATATCTCCCCCAAGTGAGGTTGAAAGCAGCCACTCAGGCCCCTCCCTGGGTGCTCATTTCACCAACGTTTGCTAACCGGCAGCAGCAGCTGGACCAGAAGAGGGTGGGGAAGAAGCTGGGCCTTTTATGTCTTTGGTTTTTTTAACTGGGCAGAAACACACCTGTGTTAGGGGCCTAAGCTATGGAATAACCTTAGATGCATGGGTGAGGGCCTGGTGGCCTGTGGGCCCAGGAGGGAGCTAGTGGCAGCCACTGGTAGTGACCGAGGCAGAGAGTTCGTGCTTCTAGTCCAAGGCCACCACTCAAAGCGTGGGCCCTGGGCTAGGATCCTGGGTGGGCGTCACGTGGAGCTGGTTAACAAGGTGGAATCTTTCGCCTGTCCAGACCTACTGCATCGGAATCTATGATTTATCCAGGGTGTCTGTGCACATTAAACGAAGGCTTGAGAAGCTCTGTGCCCACCGCCTCTCGTCATCATATGCAGCCCTCTCCGTTACCCTTAATCCCCTTTAAACACCTGCCACAGATCTTTCAGTGGTGGGGACCTGGGGATGGCTCTGCTCACCTAGGCAGGTTCCACTAAGGGGCTTCAGGGCCTGCCGTAACCCCCTGCAAGGACTTTCCTCAGCTCTGAATGGCTGAGACCTTTCCATTTTAAGAACTCTTGGAGCCTGAGTAAAGCCTCATCTTTTTTTTTTTTTTTTTAATTTTTATTTAAAAATTTCGGAGTTTCGCTCTTGTTGCCCAGGCTGGAGTGCAATGGTGGGATCTTGGCTCACCGCAACCTCCACCTCCAGGGTTCAAGTGATTCTCCTCCCTCAACCTCCTGAGTAGCTGGGATTACAGATGTGTGCCACTAGGCCCAGCTAATTTTGTATTTTTAGTAGAGATGGGGTTTCTCCCTGTTGGTCAGGCCAGTCTCAAACTCCCAACCTCTGGTGATCTGCCCGCCTCGGCCTCCCAGAGTGCTGGGATTGCAGGCATGAGCCACTGCGCCCAGCCATAAATCCTCATCTGATTGCTGGCAG
Seq C2 exon
GTCTACATCTCCGAAATCGCCTACCCAGCAGTCCGGGGGTTGCTCGGCTCCTGTGTGCAGCTAATGGTCGTCGTCGGCATCCTCCTGGCCTACCTGGCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000136856-SLC2A8:NM_014580:3
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact
ORF disruption upon sequence inclusion
No structure available
Features
Disorder rate (Iupred):
C1=0.000 A=NA C2=0.000
Domain overlap (PFAM):
C1:
PF0008319=Sugar_tr=FE(20.6=100)
A:
NA
C2:
PF0008319=Sugar_tr=FE(12.4=100),PF100274=DUF2269=PU(39.7=91.2)
Main Inclusion Isoform:
NA
Other Inclusion Isoforms:
NA
Associated events
Conservation
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
GCTGTCGTGACCCTGGGT
R:
CCAGGTAGGCCAGGAGGATG
Band lengths:
304-2099
Functional annotations
There are 0 annotated functions for this event
GENOMIC CONTEXT[edit]
INCLUSION PATTERN[edit]
SPECIAL DATASETS
- Autistic and control brains
Other AS DBs:
FasterDB (Includes CLIP-seq data)
AS-ALPS (AS-induced ALteration of Protein Structure, links to PINs)
APPRIS (Selection of principal isoform)
DEU primates (Only for human)