Special

HsaINT0145779 @ hg19

Intron Retention

Gene
Description
sodium channel, voltage-gated, type I, alpha subunit [Source:HGNC Symbol;Acc:10585]
Coordinates
chr2:166866229-166868792:-
Coord C1 exon
chr2:166868619-166868792
Coord A exon
chr2:166866352-166868618
Coord C2 exon
chr2:166866229-166866351
Length
2267 bp
Sequences
Splice sites
5' ss Seq
GATGTAGGT
5' ss Score
4.9
3' ss Seq
TATTATTTTTGTGTGTGCAGGTT
3' ss Score
9.29
Exon sequences
Seq C1 exon
GCATTTGAAGATATATATATTGATCAGCGAAAGACGATTAAGACGATGTTGGAATATGCTGACAAGGTTTTCACTTACATTTTCATTCTGGAAATGCTTCTAAAATGGGTGGCATATGGCTATCAAACATATTTCACCAATGCCTGGTGTTGGCTGGACTTCTTAATTGTTGAT
Seq A exon
GTAGGTATCGTTCATATTTTTGTCTCTGTTCAAGGTAGCTTGTCTTATTTATATTCAAATTCTACAATAGTGAGTCTCAGACCACTATGTTATGTTGACAGACTATAATAACCACTAAACGCATATATGCAATGAGAGTGTCATTTCTGGAAGACAAGGGCTAATTTAATTCTGATTTAAAATAACATTGGGGGATGGAATCTATGGTAGTTCTCTAGTTATCTGAGAAAGCTAAAGAAAAAACAACACATCAGCAGTTTGTAGGGAAAGTAGTGAAACAGGGAACTTAAAAGGTATGTTGCTTAAATCCTTTATGTTGTGAGTCAGACAGACTCAAGTTTGTATCCCAGGACCATCACTTGTTGATTTTGTGCCACTGAGTTAGTTTCTTGGCCCCAAACTCTTGACCCCCAACTTGTACAGTATTAAAGGCACTCAATAAAAACAGTGATGCTGTTGGGTGCTACAGTCATTTAAAAAAATTCTATTTGATCTACTCAAACTTTTTAAAGAGTAGATTTAAATAGTAGATTATATGGATTATGACTTCATTATAGGAAGTAAGGTATGTAGAGTGTAGGGAAAGAGAAGTCTACTTTATTCAGCAGTGAAAGTTTTCCTAGAATGTAAACTAGATTTACGGCAAGCCCAAACAGCCCTTTATAGAATTTGTATCCCCAATGATTAATACTGCATTTACTGAAAACAAGTGACTGACTTCAAGATGTGTTAAAGTTAAGCATCATGTTTTCTATTATCAACTTGGCAAAATTTCAGCTTTAGAAAGCTACAGCAAAACTATCCTGATTTCATATTGAGTAGTTTTACCCCAAAAAGATACTAACCCAGCAAGACTATGAGGGTTTCTTGTGGAAAGTGTTTCTTGAGCTAAGAATCATGAATGCATTATATTTCCTTGACCCTGAACAAAGGCAAAACTAAGCTATTTAAAAAACTTAACAATGTTACTGTGAAATGAGCCAATTGAGAGAAATCTCAAAGGAAGAATTGCTTTATCACATCAATAAGGGAGAAAGTTTGTAATATTGAGGTTTCAAGCATTAGAAGTTACATTATGTTTCAATTTCAGAATTGTTTACACTATAATTTAAATCTAAATGTAATTTAACCCTTTAAAACTTCCTGAGGTTTTTTTTCTATTATGTTTATTACACATCAGCTTTTTCATGAAAGTTTTTTAGTGTCATTTTTGAAACATTTTAAGAAAATAATTTTATAGAAAATTTTGTAGTTTGTAACAATAATATCTTTATTTTCAATGTTCTGTTTTAATTCTTTAATGAAGATCAGTATAGCACTCTATAAAAGGACTAATTACAGCACATCTCAAATAATGTAAGAAGTATATTAAATATGATACAATTAATACATTTTAAAAAAGAAAAGTTTACAAAAATAGTGTGCAGTATATGCGGAATTCTCCAATACTAGCATCTTTCTAACCAAATAAGTTATAATCTTCCTTGAATACAAAGTTTTAGTAAATTCCTTATTTAGAGAATTAGATACGTAAGATTTTTCCTTTAGTCATGTATATTACCTACAAATGAATACAAATGAAGTAAATTTATTGCTGTGTGTATTTGGTAAATATTCATTGATTGGCCCTTTGGGGCCAGATATCATGGCAGAAGCCATAAATTAGTATAAAAAATTTTGAGGAAGTTTTGTAATGGAATTTCTTTCTAAGTTACTTATGTAAAAATAAACAAGTGAAAATGCAAGGTATTACCAAGACAAAATATCACCTTCAAAACTGATGTAGTTCATTAATTTCTGAGAATACCAATTATGATTAGTTGAATATACTGATGCACAGTAGAAACTTCCTGCTTTTTTTAGTACAACAGCAGTTTTTGTATTTTATAACTAGCTACAAGAAAAGCCTTAAATTCAACAGCAACTTAATAAAATAAAGGAAGAATAGCCAATGAATTTTTTTCCACCTTGATTTCTTCTTTTATTTTACTAATTTTTACTTTGCTTTTTTTTTCTATTTATTCAGTTGATAAATTATATGACATTTAAGGATTTTTTTTCAACTAGCTTTTAATTAATGTCCTAAAAATTACATCCTTTACATCAAACTGAAATTATTTCTTTAATTTTTTAAAGGTTTACTGAAAATGTCTGAACATTTATCCTCTGAATAATTATAAGCAAAAATTATACTTGTTGTATTATATAGCAACTACACATTGAATGATGATTCTGTTTATTAATTGTTATTATTTTTGTGTGTGCAG
Seq C2 exon
GTTTCATTGGTCAGTTTAACAGCAAATGCCTTGGGTTACTCAGAACTTGGAGCCATCAAATCTCTCAGGACACTAAGAGCTCTGAGACCTCTAAGAGCCTTATCTCGATTTGAAGGGATGAGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000144285-SCN1A:NM_001165963:19
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=PU(17.0=67.2)
A:
NA
C2:
PF0052026=Ion_trans=FE(17.5=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
No suggested primer sequences
R:
No suggested primer sequences
Band lengths:
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