HsaINT0145788 @ hg19
Intron Retention
Gene
ENSG00000144285 | SCN1A
Description
sodium channel, voltage-gated, type I, alpha subunit [Source:HGNC Symbol;Acc:10585]
Coordinates
chr2:166909362-166911276:-
Coord C1 exon
chr2:166911148-166911276
Coord A exon
chr2:166909454-166911147
Coord C2 exon
chr2:166909362-166909453
Length
1694 bp
Sequences
Splice sites
5' ss Seq
TGCGTAAGT
5' ss Score
9.73
3' ss Seq
GTGTGAACTCCCTATTACAGGTA
3' ss Score
8.7
Exon sequences
Seq C1 exon
ATACACCTTCACAGGAATATATACTTTTGAATCACTTATAAAAATTATTGCAAGGGGATTCTGTTTAGAAGATTTTACTTTCCTTCGGGATCCATGGAACTGGCTCGATTTCACTGTCATTACATTTGC
Seq A exon
GTAAGTGCCTTTTTTGAAACTTTAAGAGAGAACATAGTTTGGTTTTCCATCAGTGCTTATGCTTTTAAGAATAGGTTTGCTTTACCTGTAGAATATTTTGGTGTGATTTATACATTCAAACTCTGGATTTCAATTTAGCACAACAAAGGTCTAAGTGGAATTTCACTATAGCATGAAGGCTTTGCAGTAGTTGAAAACTACAATTTTCACACGTAGCATCAGTCAGAAAATTTCACATATGCCACTCTTCCACACACACATGCACAAACACACACACATATGAACACACACAATCTAATGTCAAAACACAAGCATATTTGTAATACATCTGTGAAAATAACTTTAAAAATTACAGCCACAAAACAGTTCTATTGGCTACACAAATTTGCAATGACCTTGCTGATATTACACACAGCTTCTTTTATTGGTTTGGTAAAATAATTGAAAGTAAGTATCTACTAGCATCAAAACGATCTGACAAATCAAACTAAGAGAAGAAAGAAGATACTTGAAATATTATGTTTTTAATATATTAAATTACTGATTTCTAAGACCTGTAGAGGAATACATTCTCTCTGCCTCTTTCTGTTTCTCTCCTGACCCCTTTTCTTTCTTCTTTTCTTCTTTCCTTTTATGGCTCTCTTCATCTCTTTAGTCTGAACATAAACTTCCTTATCCTTATCTCCTATTCATATCCACTCAGTAATATGCACAGTTTATGCACCCCAATGCTTTTTTTTCTAGTGGCAAACTTCCTCAGGAAGAGACCCAGAAAAATAATAGAAAACCATTCCAGACTAAGTGAAAGTAGAGTGTAGAAGGAGGCAGCCCAACAACACTTACCCTCATCCTTCCTTCAGGAGCTGATTTTTTGGCCTCTAACAGTTGTGATGTAGTGGATAGGAGCAGGAGAGGTGGCACTGATACACTCAGGACTCCGAATGTCTGGTCTTAATTTCCTATCTGATCAGGATGAGCCAATTCTTTGCTAGGCTCTCTGGTCACAGCTCAAAAGAAGGCCTACAGGACTTCTATTTCTTAAGAACAAAATGGCAGTAACAATAGGCGCAGCATTGGACCCTCATCAAGTATTGTTCTTAATTTGCTTAACTTTTATTTAAAAGTTACACTAGGAAAATCTTATCTCATATATAAAAGCAGTAAGGCAAACTGCCTTTTCATGCCTAAATTTCTGTTGGGTGATTTCATATATTTTTTTCTAACTAAAACCCTAAACCATAGCCAAGATTTACTTTCTTTTTACAAGTTACACATGATGTTGGTTGCATTGCTTTCCAGAGTGACAACAAGGGTGTCTACTTTATGAAGTTTACATTTAGCTAATGGCCTTAAATTATGTGAACAAAGATTAATGATGGAATCTAATTCCTGATTTACCACTTATAATATTTATCATTTAAAATCACCAAGAAGGTCTTTATAAAAGACCCATGCAAGTAATATAAATCCTGCTAAAATCTTGAATAATTCTGATTTAATTCTACAGGTTTGTAACAGAATTTGTAAACCTAGGCAATTTTTCAGCTCTTCGCACTTTCAGAGTCTTGAGAGCTTTGAAAACTATTTCGGTAATTCCAGGTAAGAAGTGATTAGAGTAAAGGATAGGCTCTTTGTACCTACAGCTTTTTCTTTGTGTCCTGTTTTTGTGTTTGTGTGTGAACTCCCTATTACAG
Seq C2 exon
GTACGTCACAGAGTTTGTGGACCTGGGCAATGTCTCGGCATTGAGAACATTCAGAGTTCTCCGAGCATTGAAGACGATTTCAGTCATTCCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000144285-SCN1A:NM_001165963:4
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:
PF0052026=Ion_trans=FE(16.1=100)
A:
NA
C2:
PF0052026=Ion_trans=FE(11.6=100)
Main Inclusion Isoform:
NA
Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
AAAAATTATTGCAAGGGGATTCTGT
R:
CTGGAATGACTGAAATCGTCTTCA
Band lengths:
182-1876
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
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)