Special

MmuINT1030762 @ mm10

Intron Retention

Gene
Description
sodium channel, voltage-gated, type V, alpha [Source:MGI Symbol;Acc:MGI:98251]
Coordinates
chr9:119515903-119517791:-
Coord C1 exon
chr9:119517348-119517791
Coord A exon
chr9:119516065-119517347
Coord C2 exon
chr9:119515903-119516064
Length
1283 bp
Sequences
Splice sites
5' ss Seq
CAGGTCAGC
5' ss Score
7.16
3' ss Seq
TGCTCATGGGGTCTTTTCAGCAG
3' ss Score
4.56
Exon sequences
Seq C1 exon
GTCCTGAATCTCTTCTTGGCCTTGCTGCTCAGCTCCTTCAGCGCAGACAACCTCACAGCCCCTGACGAGGATGGGGAGATGAACAACCTCCAGCTGGCCCTGGCTCGCATCCAAAGGGGCCTTCGCTTTGTCAAGCGGACCACCTGGGACTTCTGCTGCGGGCTCCTGCGGCGGCGACCTAAGAAGCCCGCGGCTCTTGCCACCCACAGCCAGCTGCCCAGCTGTATCGCCGCTCCCAGGTCCCCACCACCCCCAGAGGTGGAGAAGGCGCCCCCAGCCCGCAAGGAAACACGGTTCGAGGAAGACAAGCGGCCGGGCCAGGGCACCCCTGGGGATACCGAGCCTGTGTGTGTTCCCATCGCAGTGGCTGAGTCAGACACTGATGACCAGGAAGAGGATGAGGAGAACAGCCTTGGCACGGAGGAGGAAGAGTCCAGCAAACAG
Seq A exon
GTCAGCCATCTCCCCACCCGTCCTGACGGGACAGCCACCTGCTTGTATGGAGTCCAGAGAGCAGCTCCTAGCCTCACCCAGACTACCTCAGCAATGACACGGGGAGAGAGGAAGCCCCACGGCAGCTGGCCCCTCAGAAGGTGCCAACTCCAGCTTGTCCGTTTATGCCGTTAGTTAGTATTCATCCCTGGCTGACCTTACAGCCAGGGAACATGAGGCATAGCTCAGTATTCTTGATGAATACTTCCACCCCCACCCCCAGCTCTGCACATTGTCCAGCACCAGGACCAGCAGAGACAGATGTCCGGGAGAGAGAGGGCTACAGTTTGGTGTCCTTGCCACCCTCTCCTCCCCTCCTCCCATGACTGAGGCTAATTCTGAGATTTAAAAATAAGTATCCCTGAGATGGAGGTGTCGGAGACACCACTATCTTATCTCTCAACCTGTTACTTTTAACACTTAGGACCAGGGTCTGGCTAAGGCAGGGTGTCTGTCCCTCAGGTTTCCCTTGACCTGAGCTGGGCTCCGTATAGCTCCTGAGGTCCCTCGGTCAGGCGTAACCAGGTCCCCTCCATGTTGGTGGCCCTTCCTGACTGCTTCCTTAGCTAGCAGTAGCTGGGCCCAGCTCCGGGGTTCTGCTTTCTCCTGCCTCAGTTGGCCTTGTTGTAGGGGCGGTTGAGGGAGGGAGGGCTGGGATTATAGGACCACAGCTTCCGGTGTCTCCTGCACAGGAGATGAGAATTGGTTTCTGGCTGTTCCTTCTCTTCCTCGTCCCCTGGGACCAGAACAAACATGCCTGTGCACTTGTGCGGGTGCACGTGTGTGCATGAGTATGCTTGAGCGTGAGCGTGGGCGTGTGTGTGCTCGTGTGTGTGTGTGTGTTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGAATCGGTCCAGGCTAACTGCAGTATCTTCAGACTTTGAGAAGTCAGAGCATCCTCCTGAGGAGAGTTGATAGCAATCATAAGATGGGTATCGAGGGCCAGCTGCTCCCTTTCAGGGAGTCTTAAATATGCTGAGCTTTGGCTACGGGTCCTTTGCCCATACTTACCAGGAACCTCTCACTTACTGACCCAAGTCAGCAGAGGATGGGACCTTTAGTAGGTGGAGGTTCATGAAGAGGCCAGGAAGCAGTGGGCAGGGGCTGCAGCCCACAAGACTAGGGCCCTGGAGACCCCCTGCCCGGGTGTCTGGGCTCTGCTCATGGGGTCTTTTCAG
Seq C2 exon
CAGGAATCCCAAGTTGTGTCTGGTGGCCACGAGCCCCCCCAGGAGCCCAGGGCCTGGAGCCAGGTGTCAGAGACCACATCCTCTGAAGCCGAGGCCAGTACGTCTCAGGCAGACTGGCAGCAAGAGCGGGAAGCGGAGCCCCGGGCCCCGGGGTGCGGTGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSMUSG00000032511:ENSMUST00000117911:17
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.538 A=NA C2=1.000
Domain overlap (PFAM):

C1:
PF0052026=Ion_trans=PD(4.2=5.4),PF065128=Na_trans_assoc=PU(47.0=83.8)
A:
NA
C2:
PF065128=Na_trans_assoc=FE(20.1=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
CTTTGTCAAGCGGACCACCTG
R:
CCACCAGACACAACTTGGGAT
Band lengths:
345-1628
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Ribosome-engaged transcriptomes of neuronal types
  • Neural differentiation time course
  • Muscular differentiation time course
  • Spermatogenesis cell types
  • Reprogramming of fibroblasts to iPSCs
  • Hematopoietic precursors and cell types