Special

RnoINT0048830 @ rn6

Intron Retention

Gene
Description
dynein, axonemal, heavy chain 17 [Source:RGD Symbol;Acc:1563805]
Coordinates
chr10:107060768-107061314:-
Coord C1 exon
chr10:107061107-107061314
Coord A exon
chr10:107060884-107061106
Coord C2 exon
chr10:107060768-107060883
Length
223 bp
Sequences
Splice sites
5' ss Seq
GCTGTAAGT
5' ss Score
8.56
3' ss Seq
GCTCCAACTTGATTTTTCAGGAA
3' ss Score
8.58
Exon sequences
Seq C1 exon
GCCGTATCAAGGCAACCCCACATTTGACCCTGAGTTCATTCGCTCCAAGTCCACAGCTGCCGCGGGCCTGTGCTCCTGGTGCATCAACATCGTGCGCTTCTATGAGGTCTACTGCGATGTGGCGCCCAAAAGGCAAGCCCTGGAGGAGGCCAATGCAGAGCTGGCTGAAGCACAGGACAAACTGTCCCGGATCAAAAACAAGATTGCT
Seq A exon
GTAAGTGCTCGCCAACCAGGAGGCCCTGTGAGACGCCACTCCCCGCCAATCGATGTTTCTGCTTAAAACACCCTGGCACAGCCCGAGGTCACCGATTAGTAAATGATATGAACAGGAAGGCACCATAGAGCAAGCCAGGGGGGATTATGGGTTGGGGAAATGCAGGGCCTTGAGGCCCTGAGCTTCTAGGAGCTGGGAAAATCGCTCCAACTTGATTTTTCAG
Seq C2 exon
GAACTCAATGCCAACCTGAACAACCTCACCTCCGCGTTTGAGAAAGCAACAGCTGAGAAAATCAAGTGTCAGCAGGAGGCGGATGCCACCAACAGGGTGATCTCATTGGCTAACAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000003028:ENSRNOT00000004035:44
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:
PF127772=MT=FE(20.1=100),PF041569=IncA=PU(38.6=55.7)
A:
NA
C2:
PF127772=MT=FE(11.0=100),PF041569=IncA=FE(37.6=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:
GACCCTGAGTTCATTCGCTCC
R:
AGCCAATGAGATCACCCTGTTG
Band lengths:
294-517
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]