Special

RnoINT0010315 @ rn6

Intron Retention

Gene
Description
ATP binding cassette subfamily A member 6 [Source:RGD Symbol;Acc:1308998]
Coordinates
chr10:98520044-98520671:-
Coord C1 exon
chr10:98520561-98520671
Coord A exon
chr10:98520220-98520560
Coord C2 exon
chr10:98520044-98520219
Length
341 bp
Sequences
Splice sites
5' ss Seq
CAGGTAAGC
5' ss Score
9.88
3' ss Seq
TTTTAATTTCTCCTTTTTAGGGT
3' ss Score
12.21
Exon sequences
Seq C1 exon
GCTTGTTCTTCGATGTCTATGAGAGTCAAATCACAGCAGTTCTGGGCCATGGTGGAGCAGGCAAATCTTCATTGCTAAACATCCTCAATGGACTGTCTGTTCCAACTTCAG
Seq A exon
GTAAGCAGAAAGCAACACCTTGCAGACAAGCTCTCTGCTAAGGGAACAAGGGTGGATTCCACAGCTCGATGATTATCTAAAGCTGTTTCCTAGAACTATAGGACTTTGAACGGACTTCCCAGTACCCAGATTTCACAGGACTCACTTGTAGCCCATTGTGTGTTCTCTCAGAGAAAACGGGCTGCATGGTACTTAGGCTAAGAATAGTAGTAGTAGTTTTTAGCCAAGTTGTAATTTTATGTATTTGTGAGTGGATGTCACAGTTTTGTTGAGTGAGATCTCCAAATACAAATGAAATGCCGCCTTGCTAACCTTGAACTATTTTAATTTCTCCTTTTTAG
Seq C2 exon
GGTTAGCCACGGTGTACAATAAAAATCTCTCTGAGATGCAAGACTTGAAGGAAATCAGAAAGATGATTGGTGTTTGTCCTCAACATAATGTGCAATTTGATGCGCTCACTGTGAAGGAGAACCTTACCCTCTTCGCTAATATAAAAGGGATCGTTCCGCAGAGCGTAGCGCAAGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000046890:ENSRNOT00000073149:11
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:
PF0000522=ABC_tran=FE(25.2=100)
A:
NA
C2:
PF0000522=ABC_tran=FE(39.5=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GCTTGTTCTTCGATGTCTATGAGAGT
R:
GGAACGATCCCTTTTATATTAGCGA
Band lengths:
268-609
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]