Special

RnoINT0010297 @ rn6

Intron Retention

Gene
Description
ATP binding cassette subfamily A member 5 [Source:RGD Symbol;Acc:628661]
Coordinates
chr10:98583461-98584085:-
Coord C1 exon
chr10:98583959-98584085
Coord A exon
chr10:98583579-98583958
Coord C2 exon
chr10:98583461-98583578
Length
380 bp
Sequences
Splice sites
5' ss Seq
GAGGTAACC
5' ss Score
8.55
3' ss Seq
AAAACTTTTTTGCTTATTAGAAA
3' ss Score
5.29
Exon sequences
Seq C1 exon
GGCCCTCTCACAAAAAGCCAAACATAAGAAGTTTCCAGAACCACCCATCAATGAGGATGAAGATGAAGATGTCAAAGCGGAAAGGTTGAAGGTTAAAGAGCTGATGGGTTGCCAGTGTTGTGAGGAG
Seq A exon
GTAACCTGCCCTTGTTACTAAGTCATGTTCAGTGTTGTGAGGAGGTAACCTGCCCTTGTTACTACGTCATTTCAGTGTCGTGAGGAGGTAACCTGCCCTTGTTACTAAGTCATTTCAGTGTCGTGAGGAGGTAACCTGCCCTTGTTACTAAGTCATTTCAGTGTCGTGAGGAGGTAACCTGCCCTTGTTACTAAGTCATGTTCAGCCTCAATGGTAAATCACCAAGGCACTGGAATGAGGAAGAAACACTTTTCCTATGAATGTAAAATTTATATTAGACTGCCCTCTCAGAAGTGAATCAGTTCTTGGCATACATATATGAGATATGAAATGATAGATATCTAATTTGTGACTCTGTTTAAAACTTTTTTGCTTATTAG
Seq C2 exon
AAACCGGCCATTATGGTATACAATTTGCATAAAGAATATGATGACAAGAAAGATTTCCTTCACTCAAGGAAAACAACAAAAGTAGCAACAAAATACGTCTCTTTCTGTGTGAAAAAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000004378:ENSRNOT00000005848:30
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.209 A=NA C2=0.000
Domain overlap (PFAM):

C1:
NO
A:
NA
C2:
PF0000522=ABC_tran=PU(6.8=25.0)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GGCCCTCTCACAAAAAGCCAA
R:
TCACACAGAAAGAGACGTATTTTGT
Band lengths:
239-619
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]