Special

RnoINT0023500 @ rn6

Intron Retention

Gene
ENSRNOG00000013428 | Atp6v0a4
Description
ATPase H+ transporting V0 subunit a4 [Source:RGD Symbol;Acc:1305055]
Coordinates
chr4:65763912-65766952:-
Coord C1 exon
chr4:65766740-65766952
Coord A exon
chr4:65764063-65766739
Coord C2 exon
chr4:65763912-65764062
Length
2677 bp
Sequences
Splice sites
5' ss Seq
ATGGTGAGT
5' ss Score
10.13
3' ss Seq
CATGTCCTTTCTTTCTGCAGGAA
3' ss Score
13.19
Exon sequences
Seq C1 exon
GTCATTACCCAAACAGAGTCTCACCGACAGCGCCTACTGCAGGAAGCAGCTTCCAACTGGCACTCGTGGGTCATCAAAGTACAGAAGATGAAGGCCGTCTACCACGTGCTGAACATGTGCAACATCGACGTCACCCAGCAGTGCATCATTGCTGAGATCTGGTTCCCTGTAGCAGACACTAGACACATTAAGAAGGCCCTGGAGCAAGGCATG
Seq A exon
GTGAGTGGCAGGGGCAGCTATGGATGGGAGGCAAATCACATCTAGTCTCCCCAGCCCCCTGCTTGTCCTTTCTGGGGTTGTGAACGTCACAGGTGGCTTAGTGGTGGGATTATCTCTGTCTGTACCTTCACTACATTAAAAAAAAAGTTGAGACAGTGTTTCACACACTCGTGGTTGGTTTCAAACTCTTTATGTAGCTGAGGATAAACTTGAACTTCTGATTCTAGGCATACATTCCTACACCTGATTTATATAGTGCTGGGGACTGAAGCAGGGTTTAGAGCATGCTAGGCAAGAAGTCGACCCTCTGAGCTATGTCCCCAGCCCTCTACCTTCAATTCTTAATTCGGTGCAAAGGCACAGAAAAGAATCTTTTGTTCTCTAGCAGTTGAAGAACGGGCAGGCACATGTCAAGTGCTTATGTGCCAATTCTCTGTCAGCTGTGGTAACAGGTAGCACACTATGATGATGGATGTTATCACCTTATAGAGGTATAGGCTTGCCAGAGAGGCAAAAACAACCGAGCCCAGGTACTAAGAGCTCAAAGGCACAGATGACTCAGTACACACACACACACACACACACACACACACACACACACACACACACACTGTTTAGTTACTAACCCCTCGTTCATCTGCTACTTGCTCACTGGGCACAGTTGATCCAGAGCCCCCCTGGGTAGACACAGCCCTGTGATAGTAGCTTTCCTAGAAAGAGAGATAGGCAATACACATGTGTCTGGGTACACACTTCCAGGCAGCTGTGAATGGTGGGTGAAGAAAATGAGGGACATCATGGGAGAGGAACTGGTTCTTACTACCTGTTGTCCTCATCAATGAAAGAGTGAGCCCCAGCCCAAAAAATGCCTGGCGCCTGACATTTGGTACTTGATAGGTGAGAATAATTGTAATACTAATACCAGGCAGGAAGGTGCCTCATGTCATGCAAGGCCACATAGGACTTATACTTAGGGCCAGAGTGAACCTACAAGACCACAGTGAACCATATAAGCAGGAATGGTCTCTGTGGTGATGAGAGGATAGGTTGACTTGTTCCTGCTGGAAAATGTGTTATACTTGTTTGGATCATTGCATGGAGTAATAGGATGGTGAACCCCATTGGGTTGGGGACTGGTTGGAGGAAAGCCGGTCTGACTGAGAGGGAACCAGCTGGAGATGGGAAGACTTTTACAAGGCAGGCAGCTAGGCAGGTGGTGCATCTGGTAAGCTTTGAGATACTGGAGACCCTGTCTCAATGTAGAGTCATTCTGTGTCATAAGAAAGTTAAGCTTCCTATGAGACTGGCTAAAGCAGTTTCTTCAGTCCCCTGAAATGACACAGGTATCTTCCCACGCAGGTGTGGAAGGCTTTGTGTGGGTAAGAGGCAGAAGGAAGCTTGAAGGTAGAACAGGTGTTGGATATTGTCATCACCATCAACACAATCCCTTGACAAAAGCCATTGTGTCAGCTGCCATGGGGTGTGCATGGGAAGAAGCAAAGGCTTCACACCTTCCTGTGAAAGAGGTGATTCCCATTCCTCCTTAACAATATGGTGGGAAACCACTCCATCTGCTTTATGACCTGGAGTCAGTTGTTTAACTCTGCGCTGCCTCAGTTTCTTCTCTCTAAAATGGGTCTGTCTTGAGGTGTACCTCGTAACAACATCAGGGGGAATTGAGATGAAACTCTGTAAAGACCTTTGTAGTTGGAAGAGTCCCACTCACAGCACCTCTGACAGTTGCCACGGGGGTGTGGAGTGGTGGGATGGAGAACACAGAGAATTGTGAAGACTTGGGCACCTGGAGAGATGGCTTTTGTAGTCTTGGTTTCCATAAGAAGTGGGTTATGAAGGAGGCAGTGGAGGATTAAGTCAACCTTGCCCAGAAGCCTTGACTCTGAGACTAAGGTGTTTTGACATCACTCTTTAGACTGTAGGAAGCTTTGAAGAACAATGCCTTTGGTTTGTTTTATTCCAGACATGACTGGGCAGAGTGGGTGGGTGGAGAAGTCAGCAGAAAGGCTGAGGCCAGAGGAGATGGTGGGGCCCAACTAGTGTGGTAACCCAGAGAAAAGGAGTCAGGATTCCGGAGAGAGAACTATTGAGCTGGGATGGCAGCCACTGAGTCTGAAGGGGCTGAAATGGCTACAGAACAGGAATCTGGGAAAGTGGAGCCTCTGGGAAAGGAAGGGACAAGGAGGACCTAGCTGGGGCAAGTTGGTGATTCAGCTGTAGGCAGCTGGATTTTCTAGAGCTTTTGGTTCAGGACAACCTACTGGGCAGTTAGAAAAGACGTGCGAGAGAACTTGTGCCACTTTGAAAGGTAAGGATGAATTAGCAAAGTGGCTGAGCTTCTGAAGGAGAAGTGGAGAGGGGGGAGAACAGAGAATCTTCAGCTGAGGGTTGTGGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATGTGTTGGGGTCGGGGGGTAGATGGCCAGAGAACCAGGATGGATGTTGCCTTTCTGATTCTCTCATGTAAGAGATACTAGGTAAGCATTGAGACACATTTCCCTTTCATAGTTCTCTGGAAGGTCAGGAGATGTCCCAAGTTCATGTCCAGATCTGTGTGCCAGCATCCAGCTCTCCTCCATGTGCATTGGTCACATGTCCTTTCTTTCTGCAG
Seq C2 exon
GAACTCAGTGGCTCCTCCATGGTCCCCATCATGACAGAAGTGGAAACTAAAACAGACCCTCCCACCTTCAATAGGACCAATAAATTTACAGCTGGCTTCCAGAACATTGTCGATGCATATGGTGTAGGTAGCTACCGAGAGATAAACCCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000013428:ENSRNOT00000064201:9
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=0.039
Domain overlap (PFAM):

C1:
PF0149614=V_ATPase_I=FE(9.1=100)
A:
NA
C2:
PF0149614=V_ATPase_I=FE(6.5=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:
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]