RnoINT0023450 @ rn6
Intron Retention
Gene
ENSRNOG00000036814 | Atp6v0a1
Description
ATPase H+ transporting V0 subunit a1 [Source:RGD Symbol;Acc:68405]
Coordinates
chr10:88947613-88948478:+
Coord C1 exon
chr10:88947613-88947829
Coord A exon
chr10:88947830-88948370
Coord C2 exon
chr10:88948371-88948478
Length
541 bp
Sequences
Splice sites
5' ss Seq
CAGGTACGT
5' ss Score
10.65
3' ss Seq
TTGTTGTCTCTTATTTGCAGAAA
3' ss Score
10.32
Exon sequences
Seq C1 exon
CTATTTCAAGAAGCCCCTGAACATCTACTTTGGCTTTATTCCCGAGATAATCTTCATGTCCTCGCTGTTTGGCTACCTGGTCATCCTCATCTTTTACAAGTGGACAGCCTACGATGCCCACTCGTCTAGAAATGCCCCGAGCCTCCTGATCCATTTCATAAACATGTTCCTCTTCTCCTACCCAGAGTCTGGTAACGCAATGCTGTACTCTGGACAG
Seq A exon
GTACGTCAGCTCGAGGAGGGGCGTTGTAGGTGGCTACCCAGGTCACATGTAACTCTGATCTGAACAAAGCCTAGAAACGTTGTTCTGTAATACCTGGCTTTCAGTTTGTACCGTCATATAGTATGAACTAAGTAGTACCGTAGAGTCAAACCACTCCCTATACTGCCTAGCTCGGGGGTTCAGTAACGACTCCATGCTATAGAGGTAGAACTTGTAGGGCTAAGGAGTTGTAGTCCCTGAGTACAGGCCTGTACTCACAAGGCTGCGGTGGGAGAGGCCAGAGATCTAGGCAAGCCTAGTGACTTCCAAGCCAGGGTGAGTTACATAGTAAGATCCTGTCTCAAACAACTAGATGAGTAAAGGGAGCACAATGTAGATCTGCCACTTAATGGGATAGTTACTGGTTTTGTCATGGCCTCCTCATTATTTAGAGAACACAGATAATAGTCAGAGGCCAACAAAAACATATTGTTTGGGGGAAACGTGCTGCTGTTGGAAACAGTCTGTTTGGCTAGTGGATTTTGTTGTCTCTTATTTGCAG
Seq C2 exon
AAAGGAATTCAGTGTTTCCTCATAGTGGTGGCAATGCTCTGTGTCCCCTGGATGCTGCTGTTTAAGCCGTTGATCCTTCGCCATCAGTACCTGAGGAAGAAGCATTTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000036814:ENSRNOT00000055238:16
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(9.0=100)
A:
NA
C2:
PF0149614=V_ATPase_I=FE(4.4=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:
TCAAGAAGCCCCTGAACATCT
R:
CAAATGCTTCTTCCTCAGGTACT
Band lengths:
320-861
Functional annotations
There are 0 annotated functions for this event
GENOMIC CONTEXT[edit]
INCLUSION PATTERN[edit]