Special

RnoINT0023469 @ rn6

Intron Retention

Gene
ENSRNOG00000052704 | Atp6v0a2
Description
ATPase H+ transporting V0 subunit a2 [Source:RGD Symbol;Acc:621006]
Coordinates
chr12:37372183-37374054:-
Coord C1 exon
chr12:37373844-37374054
Coord A exon
chr12:37372303-37373843
Coord C2 exon
chr12:37372183-37372302
Length
1541 bp
Sequences
Splice sites
5' ss Seq
CAGGTGAGT
5' ss Score
10.67
3' ss Seq
CTTTCTCCCGGCACCCACAGGCA
3' ss Score
8.87
Exon sequences
Seq C1 exon
GCACTTCAGGAAGAAGTTCAACATCTACCTGGTCTCGGTCCCCGAGATCCTGTTTATGCTCTGCATCTTTGGGTACCTGATTTTCATGATCATCTACAAGTGGCTGGCGTACTCGGCAGAGACCTCCAGAGAGGCCCCCAGCATCCTCATCGAGTTCATTAACATGTTCCTGTTCCCGTCCAGTGAGACACACGGCCTCTACCCGGGGCAG
Seq A exon
GTGAGTGCCTCTGCCTGGTGACCACCCTGCACTCAGCAGTCTCCCATAGCCTGGGAAGAAGGAAGAGGCCAAACTCGGGAGTGAGGGAGCGTCCTGTTCTGTTCTGTTTCTCCTTTTGCAGTGTTCTCAGGCTATCATCATCTGGGGGCAGACTTCATTTAGATTTTTTTTTCCCTCAAGTTTTGCAAGACAGGGTTTCTCTGTGTCACCCTGGCTGTCCCAGACCTCACTCTGTAGACCAGGCTGACCTCAAACTCAGGTCCTCCTGAGTGCTGGGATTAAAGACGTGCACCCCCATCGGCGCCCAGCTTACATATCGTCCTTGCTCCGGGTCCCTGATACTCTCCGTATGGTTCTAATATCTTAGTGTGTGACGCCAGTGCAAGCCCCGACCTAAAATGTGTACGTTGTTACCTGTGTCTACAGGCCCGAGGTCAGCTTGGACGTCATCCCTCGGGTGTCATCCACCTGTCCTTTTTGTTGGTGTGTGTGGTATGCGGTATGTGTGTGTGGTGTGTGTATGTGGTGTGGGGTGTGTGTGTGTGGTGTGGGGTATGTGGTGTGTGTGTGTGTGGTGTGGGGTATGTGGGGTGTGTGTGTGTGTGTGGTGTGGGGTATGTGGTGTGTGTGTGTGTGTGTGGTGTGCATGTGGTGTGGGGTGCGTGTATGTGGTGTGGTGTGTGTGTGTGTGTGTGTGTGTATGGTGTGTGTGTGTGGTGTGCATGTGGTGTGGTGTGTGTGTGTGTGTGTGGTGTGCATGTGGTGTGGGGTGCGTGTATGTGGTGTGGTGTGGTGTGTGTGTGTGTGTGTGTGTGTGTGGTGTGCATGTGGTGTGGGGTGCATGTATGTGGTGTGGTGTGTGTGTGTGGTGTGCATGTGGTGTGGTGTGTGTGTGTGTGTGTGTGTGTGGTGTGCATGTGGTGTGGGGTGCATGTATGTGGTGTGGTGTGCATGTGGTGTGGTGTGTGTGTGTGTTTGTGTGTGTGTGGTGNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNAGGCTTTGAAAGTGAGCTCTAGGATCTGACTCAGCTGGACCGAGTCATTTCCCCAAGCCTCCACTTAGAGTTTTTATAATGGTTTTTACTGCTACAATTGTGAGTCAGAAGTGCAGAGGGTGAGCCGGCCCCTGGCCCAGAGTTGCTCAATCCCCGCCCCCAGGCTGCTTCACATCCCATGGCGGAGCCACCTTTCATCTCCGTGGACTTCTTTCTCCCGGCACCCACAG
Seq C2 exon
GCACACGTCCAGAAGGTGTTGTTGGCTCTCACCGTGCTGGCTGTCCCTGTGCTCTTCTTGGGAAAGCCGCTCTTTCTGCTGTGGCTGCACAATGGGCGCAGTTGCTTCGGCGTGAGCCGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000052704:ENSRNOT00000083401:15
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:
PF0149614=V_ATPase_I=FE(15.8=100)
A:
NA
C2:
PF0149614=V_ATPase_I=FE(4.8=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:
GGAAGAAGTTCAACATCTACCTGGT
R:
GCTCACGCCGAAGCAACT
Band lengths:
320-1861
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]