Special

MmuINT0050627 @ mm10

Intron Retention

Gene
Description
dynein, axonemal, heavy chain 10 [Source:MGI Symbol;Acc:MGI:1860299]
Coordinates
chr5:124817989-124819410:+
Coord C1 exon
chr5:124817989-124818136
Coord A exon
chr5:124818137-124819130
Coord C2 exon
chr5:124819131-124819410
Length
994 bp
Sequences
Splice sites
5' ss Seq
CGGGTGCAG
5' ss Score
-0.19
3' ss Seq
CTCCTGCCTCTCACCTGCAGGTT
3' ss Score
12.46
Exon sequences
Seq C1 exon
GTGGGGCTCCCAGGGCCTTCCCCCCGATGAGCTCTCGGTTCAGAATGGCATCCTTACAACCCGGGCCAGTCGCTTCCCACTCTGCATCGACCCCCAGCAGCAGGCCCTCAACTGGATCAAACGAAAAGAGGAGAAGAATAACCTACGG
Seq A exon
GTGCAGTCCCTCTGCCTAAAGTCCCTGCCCCATCCTGAACTCCACCTGAGGACTGAGCAGCCCCTTCCTCTGCTTAGGGGCTCAGGATGAAGACCATACCTTCTGTCTTTATTTCTCTCTGCTTGGTGGTCCAGGATGCTCCACTGTGTGTGTCTGGGTGGGGAGAAGGAGCTAGTGGAGGAGGGAGGCTAAAGTGGCAGCTTTATTTAGAGGTGACCCACTTAGCAAGTCTCACGCTCACTCAAAGCAGACACGTCTGTGGCTTTTAAAGAGTATGTGCAGAATCCTATAACAGTTAACAGAGTCAGTTTAGAATATTCTTATTAACCCCATCCTTATCCCAACCAAGAACAATGATGTTTCCCTTAGTGGTTGCTGCCCAGCCAGTGGCAACTGCTAATACAGTTTCTGTCTCCATGGCTTTGCCTACTCTTGATATCTCCTATGGATAGAAGCATTTAGTAGTTAATCATTTGTGGTTGGCTTTTTTTATGATGTAGGGGTTCAACGATGTCGTAGCAGGTGTAGGTACTTTGTCCCAACCTCTTTATCTTCTTTATAGCTGTATAGTATTCCTTTGTATGGACATACCACATTTTGTTACTCCAACCTCAGTTGATGAACAGGGTTGTTTCCGTTTTATGGTGCTGCTGTGAACATCTGTATACACACTTCTTTTTCATGCATGTTTGTTGTTGGGGGCGGGGGAGGGTCACGAATGTGTAGTCAGAGGGGAACTTTTCAGAGCTGATTTTCTCCATCTACCCTATGAGTTCAGACTTGCATGGCCTTTACCCACTGAGCCACCTCACCAGCCCTGGTCTGTGTCCACATTCATGGTCCTCCAGGGCACGCTCCAGGAGTGGGATGGTTGGGGCGCCAGCTTTTGTTGAGCTACCAAATTAGTGGTCTCCAGTTTTGTCCTATGCTTGCTTTCCTGGCCCTTGCTTCCCACTTGACCTGGCACACCCCACCTCCTGCCTCTCACCTGCAG
Seq C2 exon
GTTGCTTCCTTCAATGACCCCGACTTCCTGAAGCAGCTCGAGATGTCCATAAAGTATGGGACCCCCTTCCTGTTCCACGACGTGGATGAGTACATCGACCCTGTGATTGACAGCGTCCTGGAGAAGAACATCAAGACCTCCCAAGGCCGCCAGTTCATCATTCTGGGGGACAAGGAGGTTGACTATGACTCGAATTTCCGGCTGTACCTCAATACCAAGCTGGCCAATCCTAGATACTCCCCATCGGTGTTTGGGAAGGCCATGGTCATCAACTATACTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSMUSG00000038011:ENSMUST00000141137:61
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:
PF127812=AAA_9=FE(21.2=100)
A:
NA
C2:
PF127812=AAA_9=FE(40.3=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:
GAGCTCTCGGTTCAGAATGGC
R:
TCTAGGATTGGCCAGCTTGGT
Band lengths:
354-1348
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