Special

RnoINT0133924 @ rn6

Intron Retention

Gene
Description
seizure related 6 homolog like [Source:RGD Symbol;Acc:1563628]
Coordinates
chr12:50222916-50225966:+
Coord C1 exon
chr12:50222916-50223110
Coord A exon
chr12:50223111-50225774
Coord C2 exon
chr12:50225775-50225966
Length
2664 bp
Sequences
Splice sites
5' ss Seq
AGAGTAAGT
5' ss Score
9.35
3' ss Seq
ATGTGTTCTTCTCTTGGCAGTTA
3' ss Score
9.63
Exon sequences
Seq C1 exon
AGGTGTCACGGAACGACTCCTGCTCAGACTTGCCTGAAATTCAGAACGGCTGGAAAACCACTTCCCACACGGAGCTGGTCAGGGGAGCCCGGATCACATACCAGTGCGACCCTGGCTACGACATCGTGGGGAGTGACACCCTCACCTGCCAGTGGGACCTCAGCTGGAGCAGCGACCCCCCGTTTTGTGAAAAGA
Seq A exon
GTAAGTCAGCTTTCTTCTCCCTAAGTTGTTGAGTAGAAAAAGCCACCCCCAAGGGCACATGCCACATGGTGTCAACCACATGTTTAAGGTAGGAGCTGGCTTCCTCTCTTGAATATTGGAACCCTGGTTTCTGGTGCCTACAACCTAGTGGAAACGTGAATAAATAAAGTGCATGGGGTGGAGGGTGACAGGGGCAGTGGGGGCTGTAGTAAATGATAGTGTGTCCAGCCTGTGTGGAAGCCATGTTGACTCTTCAAAGCCAAACCCATCCTGCTCCAACTTTACCTCCCTCCTAGGCAACTAGCTTCCTTCCTGCTGACTTTAGGATGCTGCCCCAGGAGTACAGGGCCAGCCATGAGTAGTGGCTATGCTCTTCGTCCTGAAAGGGGGATAAGAAAGGGAGTGCTGCTGGCTTCTCCCTGGTGTCCTACAACAAGGGAAGGAGCTGAGCCTGCAAGCCGCTGGCCTCTCCTCCCAGCATCGAAGTCCCAACCCCAACCCTGTTGCAGGGGATGTCAGGGTGATAGTCTGATATTCCTGTTTCTCATGATCAGAATCAGAACAGCTCAATAATGACATATGTCGGCAGAGGATGAGGGGGATGGGAAGGGATAGGGCAGGAACTGGGCCATGTAAGAAAAAAGACAGCAACCGGGCAACACAGGGAACTCTACTGAAGAGCTGCAGTCAGTCACATGTGCACACACACACACACACACACACACACGAGAACAGGTGTGGAGCCTGCAGCACCTGGCACACTCAGACAGACACAGGCAGGCAGGTAGGTGGGTGAATGGATGGATGGACAGATGGATGAATGGATAGATGGATGGACAGATAGGCAGATGGGTTGATAGGTACAGATGGGCCAGGTCTGTGACATTTCCTGTGTGAGTATTTCTCTGTATCCATGTATAGATGTACACCTATATCTGTGTGTGTGTGTGTGTGTGCGTGCATATGTGCATGTGTGTGGAATAACCCTGGACATGGATATATATGCAGATAAAATGGAGTTGTAGACCATATGTTTAATATACAATGTGTATGATATATACATATACATTATACATATACATACACATGAGGTAAGTAACACAACTGTATGTGGCATATAATATGTCTCTCTATATCTACATAAAACTATATCTAGATGGATGGGTAGACAGACAGATGGACAGATACAGACAGATAGGTACATAGGTGGCTACATGAATAGACAGATAGATAGGACCGACGGATGGGTGGCTAGACAGACAGACAGCTTCAGGTAGAAATAACTGCAAATAGATACTGCATGTGAAGGGATGAGCAAGAAGGGATCCGTGTGAAAGGATGCGTGTGAAGGGATGTGTGTGAAGGGATCTGTGTGAAGGGATGCATGTAAAGGGATGAGCGAGAAGGGATGCGTGTGAAGGGATGCGTGTGAAGGGATGCGTGTGAAGGGATCTGTGTGAAGGGATGTATGTGAAGGGATGCGTGTGAAGGGATGCGTGTGAAGGGATGCATGTGAAGGGATGTATGAGAAAGGATGCGTGTGAAGGGATGCATGTGAAGGGATACGTGTGAAGGGATGCGTGTGAAGGGATGCGTGTGAAGGGATGCGTGTGAAGGGATGTGTGTGAAGGGATGCGTGTGAAGGGATGTGTGTGAAGGGATGCATGTGAAGGGATGTATGAGAAAGGATGCGTGTGAAGGGATGTGTGTGAAGGGATCCGTGTGAAGGGATTCATGAGCATCAACTGTCCATGGCGGCTCTGACTAGGATGGTGGACACTGTTCACATCACTCAGGTGTTCACTTCCTTCCTTTTTAATTAGTTTACTGTTTCCCTTTTATCTGTATTGATTTTTTAATTAAACTGTAATTGATGCTTGTTTTCTAGTGTCAGGCATCACAGAGAGAAGAGGGGCAACCCTCACTCGGTTCCCTCCACTCTGGACATTGTTCAGAATTTCATGGAATGGAAGCTCAAACTGAGCTGTCCCCTTTCCACCATGCTCCCCACCTGTGCTCCCCCTCTTCCATGCTCCCACCATGCTCACCCTCCTCACAGTGCCCCCACCCATGCTCACCCTCCTCACAGAGCTCCCCACCCAGGCTCACCCTCCTTACAGTGTTCCCCACCCATGCTCACCCTCCTCACAGAGCTCCCCACCCATGCTCACCCTCCTCACAGAGCTCCCCACCCATGCTCACCCTCCTTACAGAGCTCCCCACCCATGCTCACCCTCCTCACAGTGCTTTCTGCCCATGCTTACCCTCCTCACAGAGCTCCCCACCCAGGCTCACCCTTCTCACAGAGCTCCCCACCCATGCTCACCCTCCTCACTGTGCCCCCACCCATGCTCACCCTCCTCACTGTGCCCCACACCCATGCTCACCCTCCTCACTGTGCCCCCACCCATGCTCACCCTCCTCAGTGATGATGTATACTATAGCAGTAGGTTCAAGACCTAGTGGAAAATCCTGGGACACATTCAGGAATAGCATTCTGGGTCTCTTCCCGCCTGTCCTGTTCTCCAACCACTTCTTTGTATCTGCGTGCTGTGTCCTCAAAGGGCCAAGGGCTGACTTGGGAAGCTTTCACAGGAGAAGATCCTCCTGTAAACCTTGGTGACCTGTGCATCACTGTGTGTCCATGTGTTCTTCTCTTGGCAG
Seq C2 exon
TTATGTACTGTACTGACCCCGGGGAGGTAGAGCACTCCACCCGCCTCATCTCAGACCCTGTGCTGCTAGTGGGCACCACCATCCAGTACACCTGTAGCCCTGGGTTTGTGCTTGAAGGGAGCTCTCTTCTCACCTGCTACAGCCGCGAGACAGGAACTCCCATCTGGACGTCTCGCCTGCCCCACTGTGTCT
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000025612:ENSRNOT00000032193:11
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:
PF0008415=Sushi=WD(100=84.8)
A:
NA
C2:
PF0008415=Sushi=WD(100=92.3)


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:
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]