RnoINT0023471 @ rn6
Intron Retention
Gene
ENSRNOG00000052704 | Atp6v0a2
Description
ATPase H+ transporting V0 subunit a2 [Source:RGD Symbol;Acc:621006]
Coordinates
chr12:37370867-37371738:-
Coord C1 exon
chr12:37371619-37371738
Coord A exon
chr12:37370985-37371618
Coord C2 exon
chr12:37370867-37370984
Length
634 bp
Sequences
Splice sites
5' ss Seq
GAGGTGAGC
5' ss Score
8.7
3' ss Seq
TGCTGTCTGTTGTCCCTCAGTTT
3' ss Score
9.22
Exon sequences
Seq C1 exon
AGCGGCTACACGCTCGTGAGGAAGGACAGCGAGGAAGAGGTGTCTCTCCTAGGCAGCCAGGACATAGAGGAGGGGAACAACCGCATGGAAGAGGGCTGCCGAGAAATGACCTGTGAGGAG
Seq A exon
GTGAGCTCTGAGCTGATAGGACGGGCGGGCGAGGGAGGAAGCTTTTCATTGGCTGCTTAATTCGGACTAGCTAGACTTCTGTGGTTGCCTGATGATCATTACATAACAGAGCTGCCATTCAGGATGTTCATAGAGCAAAGAAAGCGGTGAAGCACCACCAGGGTCCACAGGGCACCTATGGCGGGGAAATGTCCATTTGGATTCTGTGTAATTCCAGAGGCTGGCTCAGATGTCATTGAGATCACTAACCATGTGGCCCTCGTGGCAGTTGGGGTTCCGGGCTGGTGTTTGGCTTAAAGAAAGGAAACTGAACCTTGAGAAAAGTTGGGGAGATGGGTTGGGGAGCATCATAGCCCTACTGAGAGCAGGACTTACACCGTGGATCTGCTGGGGTTTTTTTGTTTTTGTTTTTTTTTTGTTTTTGTTTTTGTTTTTTTCTTTTTCTTTTTTTCGGAGCTGGGGACTGAACCCAGGGCCTTGCGGTTTGCTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCAACCCTGGATCTGCTGTTTTTAGTTCCCAGCATGCTCTGCCCTGAGGCCAGCCAGGGATTCATGATGGAGCAGGTGTGTGCTATGGTGTCTAATGCTGTCTGTTGTCCCTCAG
Seq C2 exon
TTTAACTTCGGGGAGATCCTGATGACTCAGGCCATCCACTCCATCGAGTACTGCCTTGGCTGCATCTCCAACACTGCGTCCTACCTGAGGCTTTGGGCTCTCAGCCTGGCACACGCAC
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000052704:ENSRNOT00000083401:17
Average complexity
IR
Mappability confidence:
NA
Protein Impact
ORF disruption upon sequence inclusion
No structure available
Features
Disorder rate (Iupred):
C1=0.044 A=NA C2=0.000
Domain overlap (PFAM):
C1:
PF0149614=V_ATPase_I=FE(4.8=100)
A:
NA
C2:
PF0149614=V_ATPase_I=FE(4.8=100)
Main Inclusion Isoform:
NA
Other Inclusion Isoforms:
NA
Associated events
Conservation
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
CTCGTGAGGAAGGACAGCGAG
R:
GTGTGCCAGGCTGAGAGC
Band lengths:
222-856
Functional annotations
There are 0 annotated functions for this event
GENOMIC CONTEXT[edit]
INCLUSION PATTERN[edit]