Special

MmuINT0139803 @ mm10

Intron Retention

Gene
Description
sodium channel, voltage-gated, type VIII, alpha [Source:MGI Symbol;Acc:MGI:103169]
Coordinates
chr15:100971520-100972960:+
Coord C1 exon
chr15:100971520-100971661
Coord A exon
chr15:100971662-100972753
Coord C2 exon
chr15:100972754-100972960
Length
1092 bp
Sequences
Splice sites
5' ss Seq
CTGGTGAGT
5' ss Score
10.1
3' ss Seq
ACGTGGCCTTCCTCTTTCAGACC
3' ss Score
11.57
Exon sequences
Seq C1 exon
GCAATGCCCAGAGGGGTTCCAGTGCATGAAAGCAGGAAGAAATCCCAACTACGGCTACACCAGCTTCGACACCTTCAGCTGGGCCTTCCTGGCACTGTTCCGCCTCATGACTCAGGACTACTGGGAGAACTTATACCAGCTG
Seq A exon
GTGAGTACACTGGGGTATGGCAAGCTGGGGACTTTCTGTGCGACACACCCATACTGCAGACATTAAGTATGATCTGGGAACGGCGTTTCTCGATCCCTCGGGATGGATGAATTCAGCCAGCTCTTAGCCCAGTTTCTTGACTGTTTAGTCAGCTGTGGAAGCTGACACCCCGACCGCCTCAGAGCGCCTGCTTCCTCTCAGGTTGCTCTCCGCAGTGTGCATCTTCTTTTGGACTTCTGCTGTCAGCACGTTTGTTTAAGAAACAGCAAACACTTGTTTGTGCAGGGCCCCTTCCTAGGTGCTTAAATGATGGGGTCTCTCTCCAGAGGACCTTGAAGTATGACTTATCAATATTTTTAGAGCCATACTGCATTTGGTCTTGTTCAGGTGTGTGGTCCCCATTCCAAGATGACTTCATTGTCTTGTAACTCACAAGTCATAATGAGGGAACTGGTGGCGCTGATTTGCTAACCTTAGAAGTCCTGACAAGCCACTGCATTTGTCTCTGGCTGATGATGCTGGTTGGTTAGAGGACAGAAAATAACTCTCCCTCTGCAAAAAGGAGCCTCTTTAAGAGAAGCTTCAGTTTCCAATCCCCAAGTCAGTCCTTACTGTTGAGCATAACAGACACAAAATCCCACTAAGTGCTTGCTGACTGAAAGACTCAAGATGAGCCAGGCCTGTGGTGTAGGTTAAGATCCCCGTGCTCAGGAGACGGGGGTGGGGGAGGGGGTATGGGGGTGTGGGGTGGGGGGGGTGGGGGGTGGGGGTGGAAGGAGGTAGGAAGGTCACTGGGGAGTTTGAAACCAGTCTGATTTACATAGCAAGCTCCATGCCAGCCAGGGCTACATTGCAAGACCTTTTCTAAAACAGACAGGCAGACAGAATATTTTTCTGTGAAAGCAAAATACAAGGAGACATTCTTCTACAATGGAAGTGAGAGATAAGCAATAGGAAGACATTTGACCACTGGGATATGGAGTGGGAGCAAGGTACCATGCAAGGAAACTCTGAGCCCCCCCCCCCCCAAGCCGGCATCAGTCCCTGCTGAGGAACCCGGCTCACACTGAGAACGTGGCCTTCCTCTTTCAG
Seq C2 exon
ACCTTACGAGCGGCTGGGAAAACGTACATGATCTTCTTTGTCTTGGTGATCTTCGTGGGTTCTTTCTATTTGGTGAACTTGATCTTGGCTGTGGTGGCCATGGCTTACGAAGAGCAGAACCAGGCAACACTGGAGGAGGCAGAGCAGAAAGAGGCAGAGTTCAAGGCGATGCTGGAGCAGCTCAAGAAGCAGCAGGAGGAGGCGCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSMUSG00000023033:ENSMUST00000108909:9
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=0.072
Domain overlap (PFAM):

C1:
PF0052026=Ion_trans=FE(18.7=100),PF057587=Ycf1=FE(16.2=100)
A:
NA
C2:
PF0052026=Ion_trans=PD(12.4=44.9),PF057587=Ycf1=FE(23.4=100),PF0043013=ATP-synt_B=PU(72.1=89.9),PF0310514=SPX=PU(20.3=58.0)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
CCAGAGGGGTTCCAGTGCAT
R:
CTGCGCCTCCTCCTGCTG
Band lengths:
342-1434
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Pre-implantation embryo development
  • 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