Special

HsaINT0145880 @ hg19

Intron Retention

Gene
Description
sodium channel, voltage-gated, type IV, alpha subunit [Source:HGNC Symbol;Acc:10591]
Coordinates
chr17:62048522-62049210:-
Coord C1 exon
chr17:62049082-62049210
Coord A exon
chr17:62048614-62049081
Coord C2 exon
chr17:62048522-62048613
Length
468 bp
Sequences
Splice sites
5' ss Seq
GGCGTGAGC
5' ss Score
2.44
3' ss Seq
CCCCTCCACCCCCTACCCAGGTA
3' ss Score
8.1
Exon sequences
Seq C1 exon
GTACACCTTCACAGGGATCTACACCTTTGAGTCCCTCATCAAGATACTGGCCCGAGGCTTCTGTGTCGACGACTTCACATTCCTCCGGGACCCCTGGAACTGGCTGGACTTCAGTGTCATCATGATGGC
Seq A exon
GTGAGCAGGGGCCCCAGGACATCCTGAGGCTGGGGTGGGTGAGGGGAGGGGGCCAGGCCTTAAAGAGGGAAGCTGCCTGGGCTGAGGGCTGCAGGGGACATCGGTCAGTTGTGCAGATGGGGAGCTGCACAATTCTAGAAGCTGCCATTCTCAGGGTCTGGCTCAGCACTCTCCTGATGGACTCCTGATAATCACATGAGGCAGCCCTGACCCACAGACCCATGGGTCCTCACCTGCTGGGTGAGCCGGGCTATCTTTGCCATCCCCACTCCCCCAGAGCTCCTGCACTGTCCTTCCCAACCCTTGGGCTCCCAGAGGAGCTTTGGGGGTGTCTGCCCTGCCCCCCAGACCCTGTGGTACCCCCAATTTCTTGGGAATCCTCATCCCAGGCCTGGAGGAGCCCTGATTTCTGTCCTACCACCCACCCCAGGCTCTGACAGTCCCCACCCCCCTCCACCCCCTACCCAG
Seq C2 exon
GTACCTGACAGAGTTTGTGGACTTGGGCAACATCTCAGCCCTGAGGACCTTCCGGGTGCTGCGGGCCCTCAAAACCATCACGGTCATCCCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000007314-SCN4A:NM_000334:4
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(14.9=100)
A:
NA
C2:
PF0052026=Ion_trans=FE(10.8=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
ACCTTCACAGGGATCTACACCT
R:
CTGGGATGACCGTGATGG
Band lengths:
217-685
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