Special

RnoINT0048793 @ rn6

Intron Retention

Gene
Description
dynein, axonemal, heavy chain 17 [Source:RGD Symbol;Acc:1563805]
Coordinates
chr10:107101965-107102474:-
Coord C1 exon
chr10:107102383-107102474
Coord A exon
chr10:107102092-107102382
Coord C2 exon
chr10:107101965-107102091
Length
291 bp
Sequences
Splice sites
5' ss Seq
GAGGTGGGT
5' ss Score
7.07
3' ss Seq
CTTCCCCTCCTTCCCCTTAGCTT
3' ss Score
10.47
Exon sequences
Seq C1 exon
GCCCTGATGGAGGATGCTGTGAAAACACCAAACGTGGTGGAAGCCACCAACAAGCCGGGCCTCTACGACAAACTAGAGAGGCTGAAGAAGAG
Seq A exon
GTGGGTCCTCACCCCATCGGTCCAGCTGAGGCGTTGACAGGGCAGGTCATGCGCCACCTGCTGTGCAAAGTCACAGGTTACAGGCTAATAATATTCCATCCCTGAGGTGGATTAGGACACACCCACACACATCCCTGTGTGATCGGAGGTGGTTGGTGGAGGATGGGGACATCTGGAGACCAATTGGGTCTGTGGAGAAAAACTAGATGCCCTCAGTAAGCTTAGAGCATGGACTGGCCAAGAGCCCTACAGAGAAGGACCCACCAGTCCCCTTCCCCTCCTTCCCCTTAG
Seq C2 exon
CTTGGCTGTGTGTGAAAAGGCGTTGGCTGAATATCTGGAGACCAAGAGGCTGGCGTTCCCACGGTTCTACTTCGTCTCCTCCGCTGACCTGCTGGACATTCTCTCCAACGGAAACGATCCCGTGGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000003028:ENSRNOT00000004035:10
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:
PF083938=DHC_N2=FE(7.2=100)
A:
NA
C2:
PF083938=DHC_N2=FE(10.1=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Primers PCR
Suggestions for RT-PCR validation
F:
CCCTGATGGAGGATGCTGTGA
R:
GGGATCGTTTCCGTTGGAGAG
Band lengths:
212-503
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]