Special

MmuINT0050682 @ mm9

Intron Retention

Gene
Description
dynein, axonemal, heavy chain 11 [Source:MGI Symbol;Acc:MGI:1100864]
Coordinates
chr12:119274863-119277264:-
Coord C1 exon
chr12:119277137-119277264
Coord A exon
chr12:119275012-119277136
Coord C2 exon
chr12:119274863-119275011
Length
2125 bp
Sequences
Splice sites
5' ss Seq
AAGGTGAAA
5' ss Score
4.51
3' ss Seq
CCACATGCTGCTCATTGTAGGTG
3' ss Score
7.2
Exon sequences
Seq C1 exon
GTCTCTTCTCATCCATTCTGAGAGAGCAGGCAAATCTCACACATGATGGGCCAACCTGGATAGTCCTGGATGGGGATATTGACCCCCTGTGGATCGAGTCCCTGAACACAGTGATGGATGATAACAAG
Seq A exon
GTGAAAGACACTGTAGTGCCTCTCCTTGGCGCTATATCCGGGGGCTGTTCAGCTGCTGATATCCACAATCTCCTGTCTCCTCAATGCACTATTTCATATGTAGTCACTGTTTTGATGAGTGATATTTTCTTCATAGTTAAACAAATGATGGTTGGGGGGTGGGGGGTGGGGGAGAGGGCTGGAGAGATGACTCAACACCAACTGCTCTTCCAGAAGTCCTTAGTTCAATTCCCAGCAACCACATTGTGCCTCACAACCATCTATAATGAGATTTGATGTACTCTTCTAGTGTGTGTCTGAAGACAGCTGCAGTGTACTCATATAAATAAAAATAAATAAATCTTTTTTAAAATTTGGGGAATGTTTCCCTTATCTCTGAATTGAATCACCATTCATAAAATTTAGGCACATAGATAAGAATTCAATTTATGTGCCTTATTGTTTTCTAAGAGGCAGGTATTAAATTGCTATATCTTATGTGGTCTGATTAAATATTGATATTGAGACAACAAAAGAATGAGTTTGTACCATGTGATCACTGATGAAACCTGGCAATGCAAATTAAGTTGTTCCTATGGCTACAGATTGTGTTTAAATGCTTTGCCAAGCATGCCATGTGATTGTCCTGGGAACAGCAGAGACAAGAGGTCCCGTGTCATACCAAAAAGGCAATCCGAGACCTGTTGTTGGAGCAGGGTAAGAGTTCAGGAGCCAATACTACTCCTAGGTAGCATCAGTAGCCACTGCTTTCTGAATGAAGACAATGCTTCTCAGAAAACAGAGGTTGGAGCCTACATACATGTATGAGAGAGGACAGGACACTGGCTAACTGCAGTGGTGCACATTCTTAGTTGTGGAATACAGGTCTTTTTTTTTTTTTTTTAAGATGTCAAAGGTGTTATTTACTTTTTAAAAAAAATTTATTAGATATTTTCTTCATTTACATTTCAAATGCTATCCCAAAAGTCCCCTATACCGCCCCCTGCCCTGCTCCTCTACCCACTTCTTGGCCCTGGCATTCCCCTGTACTGGGGCATATAAAGTTTGCTAGACCAAGGGGCCTCTCTTCCCAATGATGGCCAACTAGGCCATCTTCTGCTACATATGCAGCTAGAAACACGAGCTCTGGGGGTACTGGTTAGTTCATATTGTTGTTCCACCTATAGGGTTGCAGACCCCTTCAGCTCCTTGGGTACTTTCTCTAGCTCCTCCATTGGGGGCCCTGTGTTCCATCCTATAGATGACTGTGAGCATCCATTTCTATTTTTACCAGGCACTGGCAAAGCCTCACAGAAGACAGCTATATCAGGGTCCTTTCAGCAAAATCTTGCTGACATATACAATAGTGTCTGGGTTTGGTGGCTGATTATGGGATGGACCCCCAGGTGGGGCAGTCTCTGGATGGTCCATCCTTTCGTGTTAGCTCCAAACTTTGTCTCTGCAACTCCTTCCATGGATATTTTATTTCCTATTCTAGGGAGAAATGAAGTATCCACACGTTGGTCTTCCTTCTTGATTTTCTTGTGTCTTGGAAATTGTATCTTGGGTATTCTAGGTTTCTGGGCTAATATCCACTTATCAGTGAGTGCATATCAAGTGACTTCTTTTGTGATTGGGTTACCTCACTCAGAATGATATCCTCCAGATACATTCATTTGCCCAAGCATTTCATAAATTCGTTGTTTTTAATAGCTGAGTAGTACTCCATTGTGTAAATGTACCACATTTTCTGTATCCATTCCTCTGTTGAGGGACATCTGGGTTCTTTCCAGCTTCTGGCTATTATAAATAGGGATGCTATGGGCACAGTGGAGCATGTGTCCTTATTACCAGTTGGAATTCAGGTTTTATGGTAGTCCACTTACATTTGGGCTAGTAATAGTTCCTATGGCTACTGGAGGCCTGGCCCTCATGAATCTGTAAGGCAATTTTATTCCCTAAGGATTCAGCCAGAGTGCCTCCACATGGGCTCAGATATGAATTCAGGTGAGTCTACCTGTGGCTGTCCTAGTCACGATGGGCATCACTAGTAGGAGCATCATTCATTGTGATGGTCTGTTTGATGTACTGGCTCCTGGTGGTAGCACTCCTCTGGTAACCACCAACCACATGCTGCTCATTGTAG
Seq C2 exon
GTGCTGACCCTGGCCAGCAATGAACGAGTGGCCCTCAAACCTTCCATGAGGCTTCTATTCGAGACCCATCACCTGCGGACAGCCACACCAGCCACGGTCTCCAGAGCTGGCATTTTGTATGTGAACCCGCAGGATCTGGGCTGGAATCC
VastDB Features
Vast-tools module Information
Secondary ID
ENSMUSG00000018581-Dnahc11:NM_010060:41
Average complexity
IR-S
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:
PF077289=AAA_5=FE(30.7=100)
A:
NA
C2:
PF077289=AAA_5=PD(25.5=70.0)


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:
No suggested primer sequences
R:
No suggested primer sequences
Band lengths:
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