Special

HsaINT0145966 @ hg38

Intron Retention

Gene
Description
sodium voltage-gated channel alpha subunit 8 [Source:HGNC Symbol;Acc:HGNC:10596]
Coordinates
chr12:51699570-51701207:+
Coord C1 exon
chr12:51699570-51699791
Coord A exon
chr12:51699792-51701143
Coord C2 exon
chr12:51701144-51701207
Length
1352 bp
Sequences
Splice sites
5' ss Seq
AAAGTAGGT
5' ss Score
6.84
3' ss Seq
GCCTCTTCAAACTTTTCTAGCAA
3' ss Score
6.88
Exon sequences
Seq C1 exon
GCCTGAAGACAATTGTGGGTGCCCTGATTCAGTCTGTGAAGAAACTGTCAGATGTGATGATCCTGACAGTGTTCTGCCTGAGTGTTTTTGCCTTGATCGGACTGCAGCTGTTCATGGGGAACCTTCGAAACAAGTGTGTTGTGTGGCCCATAAACTTCAACGAGAGCTATCTTGAAAATGGCACCAAAGGCTTTGATTGGGAAGAGTATATCAACAATAAAA
Seq A exon
GTAGGTGGCCTCTTCTCTGCAAGAGGAATAGGAAAAGTCTATTCCTAGTTCACATGGTCAGAAGCTACCACAGGGCTTAAAAAAGTAGTTGGAGGCCGGGCGCGGTGGCTCACTCCTATAATCCTAGCACTTTGGGAGGCTGAGGCAGGTGGATCACCTGAGATTGGGAGTTTGAGACCAGCCTGACCAACATGGAGAAACCCTCTCTCTACTAAAAATACAAAATTAGCCAGGCGTGGTGGCACATGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATTGCTTGAACCCGGGAGGCGGAGGTTGCGGTGAGCCAAGATCACGCCATTGTACTCCAGCCTGGGTGGGCAACAAGAACAAAACTCCATCTCAAAAAAAAAAACAAAAAAAAAAAGAGGTAGTTGGAGCTGGAAAGGAATGGCAGTGCTACTAGAACTAGCCTTGTAAAATTATTCCTTTCCTCGACGTAGGATTGTGTTCAGAAGCTCTCAAACATCAGCCCTCTCTCTCCCTTTTTCGCATGTACCCCTAAACTTTTGCTTTGAAATTCAGGCTTAGAAGCTTGATAAAAATTATTTTTTTCCCTAGCTGAGTTACTTGGGATATTTACACATTTAGTCCAGAATGTATCTATGGAACTCAAATTTTCTTAATACTACTAAGACTATTGCAGTCGATCTAGTCTAGGGAATCAGGTGATCTTTAAGGCACTATTCAATCCTATTACAGTTGAGTAGTTTTAATCATTTTATTTGAGGAACCAAAGGAAAATTTGATGTAGTGATACTTCTTTAGACTCATGAAAAAAGTTAGAGATGTCACTATTAGTCATTCCTGAGAAAATAAAGTCAGTTTAGTAACCATAAGAAAGTGTTGCAAAGGAGATTTCGGGGACATATGCTGGAAAGGAAAACATGCCTTGTAATTTAAAATAGGACCTAGTATCTAGTGACCAATGAGCTCTAAAATATCTTTGATAAAGACACGTTGTAAGGATAGAAGAATAGAGTGGTATAAAGGGGTGTACAACTCAGAAAACTTACTTTTAGGTCCCTTTGATTCAAGTACCAGAATCTGGCATATAGATTTGAAGTATGAATGGAAGTTGGGTGTCTGTGAAAACTATATTGCATCAAGAACTTTGGGATAGCACTTTTAATTTGTAAATATATATAAGAAAATCATTAATAGGAAAGAATTCTTATCAGCTGTCACAGCTGTTGGAAAAGATTTATGAGCTAAAGTCAATAACTTTCTGCTGGGGCTAGTTAGGAACAGTGTAACCTTATTCTCTCATTCACTTAAATCTGCCTGTTCATTTCCTGCCTCTTCAAACTTTTCTAG
Seq C2 exon
CAAATTTCTACACAGTTCCTGGCATGCTGGAACCTTTACTCTGTGGGAACAGTTCTGATGCTGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000196876:ENST00000354534:7
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:
PF0052026=Ion_trans=FE(29.5=100)
A:
NA
C2:
PF0052026=Ion_trans=FE(8.4=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
GCCTGAAGACAATTGTGGGTG
R:
CCAGCATCAGAACTGTTCCCA
Band lengths:
286-1638
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