HsaINT0035256 @ hg38
Intron Retention
Gene
ENSG00000108556 | CHRNE
Description
cholinergic receptor nicotinic epsilon subunit [Source:HGNC Symbol;Acc:HGNC:1966]
Coordinates
chr17:4900990-4901625:-
Coord C1 exon
chr17:4901525-4901625
Coord A exon
chr17:4901191-4901524
Coord C2 exon
chr17:4900990-4901190
Length
334 bp
Sequences
Splice sites
5' ss Seq
CTGGTGAAG
5' ss Score
2.39
3' ss Seq
ACCGTGCCCCCGTCCCGCAGAGA
3' ss Score
11.34
Exon sequences
Seq C1 exon
CTCTCAGACGTACAATGCCGAAGAGGTGGAGTTCACTTTTGCCGTAGACAACGACGGCAAGACCATCAACAAGATCGACATCGACACAGAGGCCTATACTG
Seq A exon
GTGAAGCCCCTGCCTGCTCAGAAAAACCCGCTTCTAGACGGGGTCCAGAGAGGGGACTTCCACGGTGGGCTTGCCCCGGACCAACGACACTGGAGGATGACTTCCACAACTGGGTTTAGCTTACCCCTGTCCTGAAATCATTCTCGATTGTTACTCTAGTCCTGCCTTCTGGCTTTCCATACCCTCAACGAGAATGCCCTTTTCTGTCCGTAATTGCCCCCATCCTGACGGCCCATGACCCTGGTGCAGACAGCCGCAGCCTCCTCTTCAGCCCGCTGTCAGCTCGGCGGGCGCCCCGCTCTGACAGCCAGCTGACCGTGCCCCCGTCCCGCAG
Seq C2 exon
AGAACGGCGAGTGGGCCATCGACTTCTGCCCGGGGGTGATCCGCCGCCACCACGGTGGCGCCACCGACGGCCCAGGGGAGACTGACGTCATCTACTCGCTCATCATCCGCCGGAAGCCGCTCTTCTACGTCATTAACATCATCGTGCCCTGTGTGCTCATCTCGGGCCTGGTGCTGCTCGCCTACTTCCTGCCGGCGCAGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000108556:ENST00000293780:6
Average complexity
IR
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:
PF0293118=Neur_chan_LBD=FE(15.7=100)
A:
NA
C2:
PF0293118=Neur_chan_LBD=PD(18.0=57.4),PF0293211=Neur_chan_memb=PU(9.2=30.9)
Main Inclusion Isoform:
NA
Other Inclusion Isoforms:
NA
Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
CTCTCAGACGTACAATGCCGA
R:
GGCAGGAAGTAGGCGAGCAG
Band lengths:
294-628
Functional annotations
There are 0 annotated functions for this event
GENOMIC CONTEXT[edit]
INCLUSION PATTERN[edit]
SPECIAL DATASETS
- Autistic and control brains
- Pre-implantation embryo development