Special

RnoINT0010261 @ rn6

Intron Retention

Gene
Description
ATP binding cassette subfamily A member 4 [Source:RGD Symbol;Acc:1309445]
Coordinates
chr2:225767897-225768523:+
Coord C1 exon
chr2:225767897-225767959
Coord A exon
chr2:225767960-225768416
Coord C2 exon
chr2:225768417-225768523
Length
457 bp
Sequences
Splice sites
5' ss Seq
GAGGTGGGT
5' ss Score
7.07
3' ss Seq
TATTCTCTGTTTTCTCCTAGTGC
3' ss Score
8.82
Exon sequences
Seq C1 exon
GTTTACTCAGGCTCCTCCAGTCCAGCAGTAGATCGGTTATGTGTCGGCGTCCACCCTGGGGAG
Seq A exon
GTGGGTACCATACCAACGGACATGAAATAGCTCTCGAGAAGAATCAGCCCTCTACCACGAATCTTCTCCCTCTAAGCAGAGCTGGACAGTAAAAGTCTAACGAAAGTCAAACTTTCTACTAGATATGGCAGCAGGTGGCATTAAATTTACTTTTTTTATTTTATACAATATGCCCAAAATATAATTTCGATGTGTAATTAATATAAAATATTACTGAGATATTTTTCTTTTGTTTTGGTTCTTGTTCTAAGTCATCAAAGCCAGCGTGTTACACAGTTAGTGCCCATGTCGGTTAGGATTAGATATGTTTTGTGTTGGTACCCACACATGACCAATAATCTCAGTAATGGCAGAGGCAGGTCTAAGATGATTCTCCTAGCTCTCACACTGGCCTGGAGTCTGGCAATGAAGATGTCCTTCGTCACTAGAGCAACTCCTATTCTCTGTTTTCTCCTAG
Seq C2 exon
TGCTTTGGCCTCCTGGGAGTGAATGGTGCAGGCAAAACCACCACATTCAAGATGCTCACTGGGGACACCACAGTGACATCAGGGGATGCTACCATAGCAGGCAAGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000012892:ENSRNOT00000017878:42
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:
PF0000522=ABC_tran=PU(7.6=52.4)
A:
NA
C2:
PF0000522=ABC_tran=FE(24.1=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
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]