Special

HsaINT0145957 @ hg19

Intron Retention

Gene
Description
sodium channel, voltage gated, type VIII, alpha subunit [Source:HGNC Symbol;Acc:10596]
Coordinates
chr12:52180326-52182532:+
Coord C1 exon
chr12:52180326-52180610
Coord A exon
chr12:52180611-52182478
Coord C2 exon
chr12:52182479-52182532
Length
1868 bp
Sequences
Splice sites
5' ss Seq
GTAGTAAGT
5' ss Score
8.01
3' ss Seq
TGACTGACTCTGTTTGCCAGGCA
3' ss Score
6.51
Exon sequences
Seq C1 exon
GTGGTGGTGAATGCCTTGGTGGGCGCCATCCCCTCCATCATGAATGTGCTGCTGGTGTGTCTCATCTTCTGGCTGATTTTCAGCATCATGGGAGTTAACTTGTTTGCGGGAAAGTACCACTACTGCTTTAATGAGACTTCTGAAATCCGATTTGAAATTGAAGATGTCAACAATAAAACTGAATGTGAAAAGCTTATGGAGGGGAACAATACAGAGATCAGATGGAAGAACGTGAAGATCAACTTTGACAATGTTGGGGCAGGATACCTGGCCCTTCTTCAAGTA
Seq A exon
GTAAGTAGTGTTTTTGTTTTTGTTTTTTCAGTTCTGTGAAATTCAGGCAGCTAGCACAAATCCCATTTGGCTTCTTCTCAACCCTACTTCTAGAATCAGGATTATTCTCAATAAGTCCAAGAAAACAGTATTGTTCCCCAAACCAGTTTCAGAGAGATACCTTTCCTGAGTATTCTCTGACTTCTACAAGATCTCACTCAAAGGAAATCTCTCATTGTGCTCAGGAACAGAGCTGTGCCCAGCAACAAATAAAGATTCCTGCAGTGTAATAAAGTGGCAGAGAGATCATCTTCCCTTCCCGGTCAGAGAGTGCAGTTAAGGGCAAAAAAAATCAAGATAAGCACATAGACAAAAAAGTAATGGCAATTGTGATGGAGCAAAATAATAGTACATACTCACCACACTCCAGTTAACTTAGGAAAAAACCATGGCAGTGCCTTGGTGCCACACTCACCTCAGCTCCACCCCAGAGAAAGGTATCAGATTAATGTATCACAGTAAGGAAGGATTTAACTATCTAGATAATTTTCTTTTGCCTAATTTCATTCTTTCGTGCTTAGTTTTCACTGCCTCTCTCACCAGTGTTTCAGAATGTGTGACAAGACAACATAATGCAGTGAAAGCTCGTAGGCTTTGAAATTAGACTGTTATAGATTTGAACATACTCTGATACTTACTGGATATGTAACTTTGGACAAATTATTCAGCCTCTCTGATTCTCTGTTTCTTCATCTATTAAATATAGATAATGACACTTTGCATGGTTGTTAAGAGGATTTGTGATTTTTAAAAATTTCTTAGCACAATTCCCAGCATATAACCATGCTTAATTAATGAAAATTGCTATTAAGTATTTTTGTTACTATATTTCCATGCCTATATCATACAGTTCTTGGGAGACTAACTGCAATAACAGATGAAGCTCTCAACCTAACCTTACATATAGTAAGCACTCACTGTCAACTCATAGTAGAAGGCAAAGTTCATGGAATGAACTGTAGTTTTTCCTACCCCAAAGCTTTTTTGCTGTTGTATCCCAGTTCAAAAAATTGGACCCACAAATTGAATCCGCATTGGAGCATCTCCAGAAAACCAGTGCACATCCACAAGCCAGTCAAACATGGTAGTCACAGAGTCCCTGCCATATGCAAGATGCTGTGCTTGACAGTACAGTACTAGGGCCCTCAGATGAATAAAGACCTTCCTGTGCCCTGAAAAAACCTTAGAATCTGGTTGAGTACATAAAACACGGTGAATAGTACATGGATTATCCATATTTGTTTCCAAAATCAGTCTAGATATAGTAGACTGAAGGAGTAGAATTGGGAAGGGACTGTCAAGGATAAAGCTGGTATTGCTACTACATAGGCTATACATGTGTATATTAGTAAAGGGTAAGTCTGATCTTGTTTTTCTGTTAAATCCAACTATGAGTTTTTCCAACCCCCATCGCTTAACACCTTTTTTTTTTTTTTTTTTTTTGCTTACCACCTTTTTAAAAAATGATTCCTCAGTGGAATGGAATGCTAAGTTCCAAGCATTTTCAGTAGATTCCTGCCATTCACTCATAAAAGTTTTCCCTAACTTTAGGCAGGCTTCTCAGGCCCATGTTTTTGAGTCCTTTCGTAAAGCCTTAATCCCATTACCATTTTCAACATGTTTATTTGCCAAACTTTGTTGTTATTTTCAGGAACAAAGCCCTCCTGGGACCTGTAGTAACAAACAGAAAATTCTGTGTCCAAGGGAGGCTGCACCCAAACCCCTGTTCTGTGTTCTCACTGAACCTAAGCCTGGCCTTTGGGACCCCTGCCTAGACTCCCATCCACTCCCTTTATAGGCACCGTCTAATGACTGACTCTGTTTGCCAG
Seq C2 exon
GCAACCTTCAAAGGCTGGATGGACATCATGTATGCAGCTGTAGATTCCCGGAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000196876-SCN8A:NM_014191:22
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(62.3=100)
A:
NA
C2:
PF0052026=Ion_trans=FE(11.3=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:
GTGGTGGTGAATGCCTTGGTG
R:
CTTCCGGGAATCTACAGCTGC
Band lengths:
339-2207
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