Special

RnoINT0122922 @ rn6

Intron Retention

Gene
Description
RT1 class II, locus Db2 [Source:RGD Symbol;Acc:1595922]
Coordinates
chr20:4116941-4118506:+
Coord C1 exon
chr20:4116941-4117207
Coord A exon
chr20:4117208-4118224
Coord C2 exon
chr20:4118225-4118506
Length
1017 bp
Sequences
Splice sites
5' ss Seq
AAGGTAAGC
5' ss Score
10.22
3' ss Seq
CACCTCTTTTTCTACTCTAGCTA
3' ss Score
8.65
Exon sequences
Seq C1 exon
CACGTTTTCTGGAGCAGTTGAAGGCTGAGTGTCACTACGTCAAGGGGAGGGAGCATGTGTGGAGCGTGACCAGATTCATCTATAACCAGGAAGAGTTTGCCCGCTTTGACAGTGTCTTTGGGAAGTTCCTGGCAGTGACTGAGCTGGGGCGGCCCATAGCTGAGTACTTGAACACCCAGAAGGACATGCTGGACAATTACCGTGCCTCTGTGGACAGGTGCAGAAATAACTATGACCTGGTTGATATCTTCATGTCGAACTTAAAAG
Seq A exon
GTAAGCATTAGATGGGAAGTAGATGAGTTAAGAGGTGTGTGTGTGTGTGTGTGTGTGCGCATCTGTGTGTGTATGTGTGTGCGTATGCATCTGTGCGTGCATCTCTGTGTGTGTGCATCTGTGTGTGTGCATTTGTGTGTGTGTGCATTTGTGTGTGTGTGCATTTGTGTGTATATGTTGTGTGCATTTGTGTGTGTGCATTTGTGTGTATATGTTGTGTGCATTTGTGTGTATATGTGTGTGTATATGTGTGTGTGTGCATCTGTGTGTGTGTATGTGTGTGTATGCATCTGTGTGTGTATGTGTGTATGCATCCGTGTGTGTGTGCATCTGTGTGTGTGCATCTGTGTATGTGAGCATTTGTGTGTGTGCATGTGTGTTTGTGTGTGTGTGTGTGTGTGTGTACGCATATCTATGTATGTATCTAGGGGGTGGGGGGAGGAGAACGCTGTGTCAATGTATGTATCTGGGGCTGGGGGAAGCACTGTGTCACGTGTGTAGAAATCAGAGGACAGCTTACCAGAGTCATTCTCTCTATCCATCATGTGGTCCCGAGAACTGAATTCAGATCATCGGTCTTGGAAGCAAGCACTTTTATCTGCTGAGCCATCTCCCTAGCCCTTACTGTAATGACTTTTTAACTTTTGCTGGCCTTGGGACCCCTGAGAATCACCGCTCTCTGCTCCTGCTTCCTAGGGTAGATCCATTCCTGAGCTGTTCTGTGGTGTGTGTGCTCTGAAGTTCTGTATTCCCAATCTAGTGAACACGCACTGCTTTCAGGCATGTTTTCAAACTGAAAATATTTCAGCTCAATAATGGATTATTAGTATTTGCTAAATAAATAAATCCTTACAGGTTTTTTTTAAGATCCATTGAGCCCTGGTGTCAGGATTAACTTGGGGGACAGGTTTAGAAGCTCTGCAAGATCTTCAGCCGGGGTGGATGGAGGCAGTCAGGTAGGCACAGGAAGGACAGCTCCACCCTCATGATTTCTTCTCACCTCTTTTTCTACTCTAG
Seq C2 exon
CTAAACCCAAGGTGACCGTGTACCCTTCAAAGACGCAGCCCCTGGAATACCACAACCTCCTGGTCTGCTCTGTGAGTGACTTCTACCCTGGCACCATTGAAATCAGATGGTTCCGGAATGGTGAGGAGGAAAAGACTGGAGTCGTGTCCACCGACCTGATCTCTAATGGAGACTGGACCTACCAGACCCTGGTGATGCTGGAGACGGTTCCTCAGGGTGGAGAGGTTTACACCTGCCAGGTGGAGCATCCCAGCCTGACCAGCCCTGTCAGAGTGGAGTGGA
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000030431:ENSRNOT00000042571:2
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=0.030
Domain overlap (PFAM):

C1:
PF0096914=MHC_II_beta=WD(100=82.2)
A:
NA
C2:
PF0765410=C1-set=WD(100=87.4)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Primers PCR
Suggestions for RT-PCR validation
F:
CTGGAGCAGTTGAAGGCTGAG
R:
ATGGTGCCAGGGTAGAAGTCA
Band lengths:
356-1373
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]