Special

RnoINT0023476 @ rn6

Intron Retention

Gene
ENSRNOG00000052704 | Atp6v0a2
Description
ATPase H+ transporting V0 subunit a2 [Source:RGD Symbol;Acc:621006]
Coordinates
chr12:37388668-37390235:-
Coord C1 exon
chr12:37390098-37390235
Coord A exon
chr12:37388757-37390097
Coord C2 exon
chr12:37388668-37388756
Length
1341 bp
Sequences
Splice sites
5' ss Seq
GAGGTACGT
5' ss Score
10.2
3' ss Seq
CTGCTTCTGTGTCTTTCCAGTTT
3' ss Score
10.96
Exon sequences
Seq C1 exon
GAGCAGCTGCAGAAGCTCGAGGTGGAGCTCAGAGAAGTCACCAAGAACAAGGAGAAGCTGAGGAAGAACCTGCTGGAGCTGGTGGAGTATACCCACATGCTGAGGGTCACCAAGACCTTCCTTAAACGGAACGTGGAG
Seq A exon
GTACGTGTCCGCAGGAGAAGCATACCTGCAGGGCCCGCCACTGCTGCCTGTGTGGTTTGTCAGTTCATTTACATGGGTTGCCTTTCTGTTTAGTCTCGGCTCAGCCTTGTGTAGCCTGGCTGGCCCTGCAATCTCTGTGCAACCTGTGCCTCTGCTTCCCCAGTCCTGGAGTTAAAGCCGCCTCTGCCACACTTGGCCAGCACCCTGCTGACTGAGCTGAGCTCTCACTGGTAGCCCAGGCTGTCCTTGGAACTGGAGTGAGTGCTGGGATTATAGGCGGGAGCCTCCGTGCTTGGCATAGATGTGTATTTGCTTCGTGTGTTTTAAGTGGTCTGCCTCAGCCTCTGCTTCGCTTCCTGTGCTGCTGCTTTTAGCAGGGACACTATTTCCCACCGTGAAGTTTACAGTTGAGAAAAAGATGGTTTGGTTTGTCTTTAATTTTTTGAAAACTGTGTTTTCATGTTTTTATTACATGTGTAGTGGTGTTTTCCCTGCATATATACCCATACACTACACATGTGCGTTATAGAGGATTGTGAGCTGCCGTGTGACTGCTGGGAGTCGAACCAGGTCCTCTGGAAGAGCAGTCAGCATTCCTAACCCCTCTTTCCATCCTCTGGTGTATTTCATTATTTTGTGTGTATGGGTGTTTTGCCTACATCCATGTCTGTGGACCAAGTATGTGCAGTGCCCACAGGGCCACAAGAGGGCATCTGGTACCATGAAACCGGAGTTAACAGTTAATGAACAGCGAGCCATGTGGGCTGGGAATTGAATCCGGAAACTCTGAGAGAGCAGCAGGTGCTCTTAACCACTAGGCTATCTCTCCAGCCCCAAGCCCAATATTTTGTGGTTATGGGGAAAAAAAATCTTTGTTTTTCTAAAAGGCCGTGAATAGGGAGCATGAAGAACCCCCTCATGAGAGAAGACTGGTTCATGCTGGTGCCATGCAGGCTCGGTGGGCTGAGGGTGTTTGTGTGGATCCAGCATCACCGTGTGCTCCAAGCGCTGCATCCCAGTCAGGGCCTGCAGCACACTGAGCTGCGCATAGGATAGAGCCCGCCCGTCCCTTCCGAGGTTCCTCTCACTTGCTGTAGTAGTGACCCTAGACACGGTCTTTGTCTCCTGAGCTGAGGTGCAGCCTCACTTAGAACCGCTCTCCTCTGAGTGTCTCCAGCCGTTCGTCCACCTGTCAGGTTTGGCAGTGTGGCTTTCCTTGTGGCAGTTTACCTGTCATGGTTGTCGTCTGTTCCTGGGTGTGCAGTACCTCTGTGCGCTTGTCTGGAAGCTGGTTGTGAGGGAGGAGCCTGTTAACACGTGCCTGCTTCTGTGTCTTTCCAG
Seq C2 exon
TTTGAGCCAACTTACGAAGAGTTCCCCGCCTTAGAGAGCGACTCTCTGTTGGACTACAGCTGCATGCAGCGGCTGGGCGCCAAGCTGGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000052704:ENSRNOT00000083401:4
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(13.4=100)
A:
NA
C2:
PF0149614=V_ATPase_I=FE(3.5=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:
CTGCAGAAGCTCGAGGTGGAG
R:
CTGCATGCAGCTGTAGTCCAA
Band lengths:
201-1542
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]