Special

RnoINT0023446 @ rn6

Intron Retention

Gene
ENSRNOG00000036814 | Atp6v0a1
Description
ATPase H+ transporting V0 subunit a1 [Source:RGD Symbol;Acc:68405]
Coordinates
chr10:88942897-88943558:+
Coord C1 exon
chr10:88942897-88943036
Coord A exon
chr10:88943037-88943400
Coord C2 exon
chr10:88943401-88943558
Length
364 bp
Sequences
Splice sites
5' ss Seq
GAGGTACCC
5' ss Score
7.84
3' ss Seq
ACCTTTCCTCTGGCTCCCAGATG
3' ss Score
9.69
Exon sequences
Seq C1 exon
CTCCGTACACCGTCATCACCTTCCCCTTTCTGTTTGCTGTGATGTTCGGAGATTTTGGGCACGGCATTTTGATGACTCTGTTTGCTGTGTGGATGGTGTTGAGGGAGAGCCGGATCCTCTCCCAGAAGAACGAGAATGAG
Seq A exon
GTACCCTGCACTGGCCTGGGTGGTGTGGTCTCCCCAGCATTCATGATTAAAGTAATGATCAGAAGGCCATGAAGTTACAAAACGGGAATACTAAGTTATATGAATATTGAAGAAGCCATGTGCTGAGCAAGTGATTTATTTTAGCATTTTTCTTATTTCATTGGTAGTTCTGGGGGTGATCCTTGACGTCACTGGGGATAGGCTGGTACTCAGTGAGCTGCTTCTCTGGCCATCCTAGCCTCCTATTTTAGTTGTTAGTTAAAGCTCTCAGGGTGGAGTGGGCTGCTGTGTGGTTGGTATAAGTAACATTATCACCAGGGAAACTGCCACACTTCATTCTCGCAACCTTTCCTCTGGCTCCCAG
Seq C2 exon
ATGTTTAGCATGGTGTTCAGCGGCCGATACATTATCCTTCTGATGGGACTGTTCTCCATCTACACTGGACTCATCTACAATGACTGCTTTTCCAAGTCTCTGAATATCTTTGGGTCATCATGGAGCGTACGGCCAATGTTCACCATAGGGAACTGGAC
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000036814:ENSRNOT00000055238:12
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(5.8=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:
TCCGTACACCGTCATCACCTT
R:
GTCCAGTTCCCTATGGTGAACA
Band lengths:
297-661
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]