Special

MmuINT0050755 @ mm9

Intron Retention

Gene
Description
dynein, axonemal, heavy chain 17 [Source:MGI Symbol;Acc:MGI:1917176]
Coordinates
chr11:117948227-117949604:-
Coord C1 exon
chr11:117949444-117949604
Coord A exon
chr11:117948384-117949443
Coord C2 exon
chr11:117948227-117948383
Length
1060 bp
Sequences
Splice sites
5' ss Seq
TAGGTGGGG
5' ss Score
3.33
3' ss Seq
TCAATCAAGGTCCTCTGTAGGTG
3' ss Score
2.07
Exon sequences
Seq C1 exon
GTGGAGAGTTCGCAGGCCTTCACCTGGCAGTCGCAGCTTCGACACCGCTGGGACGAGGAAAAGAAGCACTGCTTCGCCAACATCTGTGACGCTCAGATCAAATACTCCTACGAGTACCTGGGCAACACACCTCGGCTGGTCATCACCCCACTCACAGATAG
Seq A exon
GTGGGGACCACCTACAGCCCGATGCCCTACCCCCTCCCCCACAGACCCCCCTCCCACTCCACCCCCCACCCTGGCTCTGCAGCTAGAAAAGCCCACGTTCATTTGGTGGGGAGGTCCTGTGTTGTAGAAGTTTGTAATCCTGACCTGGAGTTTCTACCCTGCTTTTGACCATTTAGTTCCCGGATAAAAGACACATATGACCGACCTTTATATTTACAATAAGCCTTAAACAGCACAAGAGCTGGGCAGATACCTACCCTCTATGCTGTTAGAATCTACTTTCCTATGGATAACCCTGAGTTGTTACATAGTAATGTTTCATCTGGGCTGTTCTTAACTCCAATTGGTCAGCCCTCAGGGCCACCTTTTTTATGGTTCACCTAACCCATAGTGGCCTCAGCCGCTGCCGCCTCCTCCTCCTCTTCCTCCTCCTCCCTCCCCCTCCCTCTCCCTCCCTCCTCCTCCTCCTATTCATCTACTCTGACCCCCAAACCTGGAAAACCTAAACCCCACCTATGTCTCTTCTACCCAGCTATTGGCTGTTGGCATCTTTATTTACCAATCAGAAATAACTTGGGGCCAGGTCACAGATCTACATGCAGACTTCAGGTCTTGGGGGCCAGGCAGGAGCCCTGCTTTAGGCTGAGCTCTTGGTCCTTCACTGGCTGTGTCCCCAAGGAGTGGCTTCACCTCCCTGAGGTCTGCAGAACAGGGAGAGAGCTACAGGAGCCCTCATGAGTGTGCAGGGACTGAATCAATTACAAGATAATAAAACCACTCAGCCCAGAGGCTGCCCAAGACACCCTCAGCATGTGTCTGACGAGTCCCCAGAGTCCGTCCCCCAAACCCACAGGAGGGCCATGTCTTGCACCCACCCCTGTCCCTCAGCACAGTGACCACCCCCCCCCACCCACACACACACATGCACACATACACACCAGCTCTGACTTTGGTCTCTGGGCCCAAGTGAGTACAGCGGCCCCACAGTAAGCCGAGCAGAGCACAGTGGGGTGTGGGTCACAGGGTCACAGTGCCCCAGGTCAATCAAGGTCCTCTGTAG
Seq C2 exon
GTGCTACATCACGCTCACGCAGTCCCTCCACCTGATCATGGGCGGAGCCCCTGCAGGCCCTGCTGGCACGGGCAAGACGGAGACAACCAAGGACCTGGGCAGAGCCCTGGGCACCATGGTGTATGTCTTCAACTGCTCAGAGCAGATGGACTACAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSMUSG00000033987-Dnahc17:NM_001167746:35
Average complexity
IR-C
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.028 A=NA C2=0.075
Domain overlap (PFAM):

C1:
PF127742=AAA_6=PU(8.2=35.2)
A:
NA
C2:
PF127742=AAA_6=FE(22.5=100)


Main Inclusion Isoform:


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
GTGGAGAGTTCGCAGGCCTT
R:
CTTGTAGTCCATCTGCTCTGAGC
Band lengths:
318-1378
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Pre-implantation embryo development
  • Muscular differentiation time course
  • Spermatogenesis cell types
  • Reprogramming of fibroblasts to iPSCs
  • Hematopoietic precursors and cell types