Special

RnoINT0023487 @ rn6

Intron Retention

Gene
ENSRNOG00000013428 | Atp6v0a4
Description
ATPase H+ transporting V0 subunit a4 [Source:RGD Symbol;Acc:1305055]
Coordinates
chr4:65747126-65750801:-
Coord C1 exon
chr4:65750683-65750801
Coord A exon
chr4:65747343-65750682
Coord C2 exon
chr4:65747126-65747342
Length
3340 bp
Sequences
Splice sites
5' ss Seq
CATGTGAGT
5' ss Score
7.83
3' ss Seq
CCTGTGTTTTCCACCCCCAGCTA
3' ss Score
9.2
Exon sequences
Seq C1 exon
ATTTGGAACCTGGCTTCAAACAAACTCACATTTTTAAACTCCTACAAGATGAAGATGTCGGTCATCCTGGGAATCGTTCATATGATCTTCGGTGTTATCCTCAGCCTCTTCAATCACAT
Seq A exon
GTGAGTTTCCTCTTTAAAAAATATTTTAAATCATGTGTCTGTGTGCATGTGCGTTTGGGTGTGGGTATGGGCATGTGAACACAGGCTCATGGACCCCCTGAAGCTGGAGTCACTGGCGATTGTGAGGTGCCTAGCGCAGTTCTGGGAACCAAACTTGGGTCCTTTACAAGGGCAGAAGGACTGATGAGCCATCTTCTACCTCTGTGTGAACGTCTCTATTGACCCTCTGCTTGCTCATCTAATGGCACCGATGAGGAAGACGACAGAGCTACCAGTGAGCCTCTGTATGGCAGGTGCTTCCTGTGGGTCTTGGCTTGAGCTGAGTTGAGATAGGCTGGTTGGCCAGAATCAGGAGCACCTTTGTGTCTGCCATGTATGTAGTCTCTCAAAGTAAATGTGTGCTTTTCACCCGAAAAATATCCTGGGGTTCAGCAGGGGCCCAGGGAGCACCTTGTGTTCCTTCTACCTGAAAGGCAAGGTTGATAAACTATAGAGCTCATTTTCCACCTAATATATCAGGGAGGAATTGTATGAATTCTGGCCAAGGTGCTCCCAATCCTGAATCATCCTGGATGTTCTTTCTCCCAGCTGGTGGCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCCTCTCCTCTCCTCTCCTCTCCTCTCCTCTCCTCTCCCTCTCCTCCTCACTCTCATCTGTTCATCTCTGCAGGTACCAGACAAATCGAACTTGCTGCCTAGGAGAAAGGGGGGCATTGGCTCACAGAAATGAGGGAGAGCTTGAATCAGTCAGTTTAGCTCCTAGTGAATGTGATCATAGGCTCAGTGCCTGACAGTGTGAGCTTATCATGCTAAACACAATAGAATGGGGGATGTGGTTCAGCTGATGCAGTGTCTGCCTGGTGTGCATAAAGCCAGGTTCAGCCTCCAACACTGCAAAACGGAATTGCACATGCAGCACTTGGGTTCCCAGAAATTCAAGGTTTAGCTACATAGCATGTTTAAGGCCAGCCTGGGCTATGGGAGATCCTGTCTTAAAAAAACAAAACAAAACAAAAAAACCCAAGGAAGTAAAGGAAGGAGAGGAAAAGGAAGATATATGACAAGACTGGGTCAGGTTACAGGAAAAAGAACAATTCCAGCTTCAATGGCTTAAGACCATGAAGCATTCATTGCAGAAGGGACCACATGGGCGCCACACCTGTTCTCCTCATACAAAGGGACTCAGAAGATGGGTGGCCACTTCCTGGAGCCCTGCAGGTGAGTTTTAAAGCTTCCCACGCAAGGTCACAGGTGCCATTTCTGGTCCCATTTTGTTGGCAAGAACCAGTTCCAGGGTGAGTGTAACTGAGAGGCCATGGATGTAGTTCTACTTGGAAGATCAAGGATGTGGAGCCCCGAGGGAAGTCTGTGAGTGAGAAGCTAAAGATCTGTGGGGAAGGTGCTTTCCAGCTGGACGTCCATTGGCCTCCTAATAGACATTGGGGACTTTTCTCTCTCTAGAGCTCCTCCCCTCTTAGCCTGGATGGGCTGTGTCTTACAGCACAAGGTCCTGACCTTTCTATTACTCTATCTTGGCCTTGTGTCTTGAAAGAATTTATAGAATTTCAGGATCGTAAAATACTCTCCTCTTTTCTTGAGGTATTAGGAACTGCACGCAGGGCTCACACAGGCTAGGTGTCTTGGGCACTGTTCTATTGCTATGATGAGACACTGACCATGGCAACTTCTGTAACAGAAACTGTTTAACTTGAGGCTTCCTTAGAGTTTCGGAGGGTTAGTCCATTATCAGCATAATGGGAAGCATGGCAGCTGGCAGGTAGGCATGGAGCCGGAGTAGTAGCTGAGAGCTTTACATCCTGACACACACACACACACACGCACACACACACACACAGACACATAGAAACAGACACATAGACACACACACACACATAGACACACAGACACATAGACACACACACACAGACACATAGACGTATACACACAGACACAGACATACACACACACACAGACATACACACAGAGACACACACACAGACATACACGGGCACACAGAGACACACATAGAGACACAGACACACACAGACACACAGGCACATACACACACAGACACACAGATGCACATACACACTCAGACACATAGACACAGAGAGAAAGACAGAGAGACACAGAGAGACACAGAGAGACACAGACAGAGAGATAGACAGGAGACCTAATACCACACCTTCTCCAACAAGGCCACACCTATTTCAATAAGGCCACACCTTCTAATCCTTCTCAAACAGTCCACCAACTGGAGACTAAGTAGGCAAATGCATGAACCCATGGGAGCCGTGCTCATCCAAACCACCACACTAGGCAACGGTTCTGCTCCTGAGCTATAGAACAGTCACAGCCCTCCTGCTTTAAAGGTGGGGTCTCACGGAGTGCAGACTGGTCTTGAACTTGGTATATATCGAAGGATGGCCCGGATTCCCAGGTCCTCCGGCTTCTACTTCCCACGTTCTGGGATGATAGAAATCATGATGCCTGGTTTTATTTTTTCACTCCTTTAGTTCTGAGACAAGCTCTCATTAAGTTGTGGAGGCTGCCCTGTGACTCACTGTGTGGCCCAGGGAGTGCTAGAACATGATTCAGATCCAGCTTTTAGTGTTTCTTTTCAATCCAATCATGAAAAAGTGAGAACCACTAAGTTGTGTGTGTGTGTATGTGTGTGTGTGTGTGAGAGAGACAGAGACAGAGAGAGAGAGAGAGACAGAGAGAAACACAGAGAGAGATGTGCGTGTGTGTGTGTGGTGGGGGGAGGGTACCAGAAAATGAAGCCATGGCACTGACGTTAATCCACCTGATGTGACTGCTGGGAATCCAACTTGGGTCCTCTCTGGAAGAGCAGTAAGTAGTCTTGATCACTAAGCCACCTCTCCAGCCTCAGAATCAGTCTTAGTTTCCAGGCTCCGTCTAGCCCATGGGCTGTAGACTGGGAGACCCTGCCTCAGCACATGCACAGGAGAAAGCTTCCAAATGTCTTGTTATTGCTTCATTTCACCTTCAAATAGGACTTAGGAGTGAAGTCTTCATGAGAAGCTGTGGCCAGATCACTGGATGGTACCCTTCTAGACCTAGGTTCCCCAAATCTGTGCCAAAGCACCCCCCCATGTTGCTTTTTTTCTCTCTCCTTTTCTTTCCATGCACATTTGTGTTTGCCAGGGGAGTACAGCTGTGTGCCGTCAGGTGCTCAAGAAGGAAATGAGCACCGTGTGCTCTAGGGGGCGCTCTTAAGCGCCAACGTTCTGTTAATGCTCCATCTTGTCTTACCTGTGTTTTCCACCCCCAG
Seq C2 exon
CTACTTCAGACGAACCCTCAACATCATTCTGCAGTTCATCCCCGAGATGATTTTTATGCTGAGTCTGTTTGGATACCTGGTTTTCATGATCATTTTCAAGTGGTGTCAATATGATGCCCACACATCCCAGAAGGCACCCAGCATCCTCATCCACTTCATCGGCATGTTTCTGTTTGACTACGATGACTCGTCCAACGCACCCCTGTACGGCCATCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000013428:ENSRNOT00000064201:14
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(5.1=100)
A:
NA
C2:
PF0149614=V_ATPase_I=FE(9.4=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:
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]