Special

MmuINT0051167 @ mm10

Intron Retention

Gene
Description
dynein, axonemal, heavy chain 8 [Source:MGI Symbol;Acc:MGI:107714]
Coordinates
chr17:30761006-30762771:+
Coord C1 exon
chr17:30761006-30761128
Coord A exon
chr17:30761129-30762640
Coord C2 exon
chr17:30762641-30762771
Length
1512 bp
Sequences
Splice sites
5' ss Seq
AAGGTTCTG
5' ss Score
2.04
3' ss Seq
CACTCCTCTTTCAAACACAGATC
3' ss Score
7.27
Exon sequences
Seq C1 exon
GTGCCGTCCTTCGAATTCCTGAGTGAAAAGCTTCAGTTCTACCAGAGGCAATTCAACGAGATCATCCGAGGGACGTCTCTCGACCTGGTGTTTTTTAAAGACGCCATGACTCACCTCGTTAAG
Seq A exon
GTTCTGTTGACTGACTATTTCCTGTGTGCGAGTGCCGTCAAAACTTAGTTCCGTAGGGGAATTACCCTGGGAGCACCCATCCCACCAGGGAGACCAGAGAAGAGCAGCCATGGATGACAGCTAGCTCACTGTTTCTAAAAACTGTGGATCACCGACGCTCATGCGTCCACTAACACAGCAGCACGTGGTTTCCAAGGGCAGGTGGATTTTGGGTCCAGAGCTCTTGGGGTTCTGATTCTGACTGCTCCCCATGCTCTGAGGAAGCTGGAATGGCCTGGGAAGAAATGCCCCTTCTCAGAAGTTTGCTTAATTGCTGTGTGTGCAGGTGTGGGTGGCCAAGCCCGCAGAGGCCAGGGGAGGATGTTGGGTATCCTGCTTTACCACACTCTCTATATCATTTCCTTGACAGGGCCTCTCACTGATACTGGTTCTCTGGAAGCCAGTCTTCTCTGGCGATCCTCCTGTCGTAATGCCAGCAGTGTGTGATCATCTCTGGCTTTTTACATGGGTTCTGGGATTTGAACTCTGGTCCCTTTGATTTCATAGCAAAGATTTTTTTTTTTTTTTTGAGACAGGGTTTCTCTGTGTAGCCCTGGCTGTCCTGGAACTCACTCTGCAGACCAGGCTGGCCTCGAACTCAGAAATCCACCTGCCTCTGCCTCCCAAGTGCCCAGCCACAGCATGGACTCTTGTCTGCTGAGCCATCCCCACAATCCTGACATGGGGATCTTGCTGCCTAGGGATAAAAAGACAAGGTTGAACATGTATACACACACACACACACACACACACACACACACACACAAATGAAATAAATGTTGAATATTATAAATGAAAAATCAGTAATGACACTTGCACATAAACACACAGAAGTTACAAAGCTAAAGAGAATGAAAGCAGATGCAAATATAGGCAGGCAAAGAAGGAACTGAAGAGGCTGCAGCCACAGCTAGCTCAGTAGTTAACAGCACGTGCTCCGCTTTTACAGTAGACCTGAGTTCAGCTCCCAGCACCCATTTTGGGTAGCTCATAACCATCTGTAACTCCAGCTCCTGAGGGTCCAGCGCCCTCTTCTAACCCCCAAGGATACCCCAACACAATGAATGTCTCTCTCTCTCTCTCTCTCTCACACACACACACACACACTCACACACAAATACACTCATACACAAACACACACACACATGCATACACACACACACACACATACTCACACACACACTTATACACACACTCACACACACACACAAACACACACTCATATACAAACACACACACACACATGCATACATACAAACTCACACACACACACACACACACATTGAAAAAATGATTTAAATAAAACATTGTGATACATTCAAACAATAACAAGAACCCAAAATGTAGCATTATAAGGAAAGAGTCTGATGTAGTCTGGAAACACGTGGTCAGACTTTGGACCCGTAAGTGTAAGAATGAATATATAAACATTTGCATCCGTTTTTCCGATAAACACTCCTCTTTCAAACACAG
Seq C2 exon
ATCTCTCGGATCATTCGAACCTCCTGTGGGAACGCATTGCTGGTGGGTGTCGGTGGCTCAGGAAAGCAGAGCCTCTCAAAACTGGCCTCCTTTATTGCTGGGTATCAGATATTTCAGATAACACTAACCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSMUSG00000033826:ENSMUST00000170651:61
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:
PF127802=AAA_8=PU(8.4=56.1)
A:
NA
C2:
PF127802=AAA_8=FE(15.8=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GCCGTCCTTCGAATTCCTGAG
R:
TCTGAAATATCTGATACCCAGCAA
Band lengths:
239-1751
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