Special

RnoINT0133934 @ rn6

Intron Retention

Gene
Description
seizure related 6 homolog like [Source:RGD Symbol;Acc:1563628]
Coordinates
chr12:50197281-50199165:+
Coord C1 exon
chr12:50197281-50197446
Coord A exon
chr12:50197447-50198998
Coord C2 exon
chr12:50198999-50199165
Length
1552 bp
Sequences
Splice sites
5' ss Seq
CAGGTGAGC
5' ss Score
9.6
3' ss Seq
TCTGCCTTTCCTCTACCTAGGAT
3' ss Score
10.74
Exon sequences
Seq C1 exon
CCCCGTGTGGAGGAGCAGTGCACAATGCCACCATCGGCCGAGTTCTGTCCCCCAGTTACCCGGGAAACACCAATGGCAGCCAGCTCTGTGTGTGGACCATCGAGGCTCCAGAGGGCCAGAAGCTTCACTTGCATCTTGAAAGGCTACTGCTGCATGAGAAAGACAG
Seq A exon
GTGAGCTGACTGCACCAACTGCTCCTCCTCAGCATAGAGAGGGTGGAGTGGGTAATCTGGGTGTGGCTGAAGCCCTGGGGAAGTTGATAAAGATCTTATGGCCCTCTGCTTCTGGTCAGTATATTGAGGCACTCTGTGGGAAAGGAGCCTTCCTGAGCCACCTAGGAAGAGAGGGAAGAAGGAGATGGGAAACATACACAAACATACACACCCTCACACATGCCCACACACAGGTACACATGCATTCGCACACACCTGCATGCACACATTCATGGGTGCACACATAGCCCATACATCCACACACAGAGACATGCACACATCCACACATGCATGCATACATACATGCATGCATACACACATACAGACACAATGCACACACACATGCACACATGTACACACTCATACCCTGAATGCACATATTCATGTTTGCACACACCTCCATACATCCACATACCCAGCAATGCATGCACACACATGCATGAACATACACATACAGGCACACATGCATATGCACACACATGCACCCTGCATCACACATTCATGCGTGCACACACACCTCCACACATCCACATACCCAGGGATGCACACACACACACACACACACACACACCTGCATGCACATATTCATGCATGCATGCACACACATGCCTGCATACATACTTACAGACACACATGCACATGCACATACATACACACAGGCATGCATGCATACACCTGCAGGCACACATTCATGCCTGCACACACACACACACACAAACACACACACACACACGCGTGCATGCATGCACACATACATGCCCACATACGCACATATAGGCCCACATGCACATGCACAAACATGCACACACATGCACACACATGCACGCACACACACACACCTGCAGGCACACATTCATGCCTGCACCTCCACATACCCACACACCCACACATCCACCCAAGCATGCATGCACACACACATGCACACATACACACATACAGGCACACACGCACATGCACTCACATGTATGTGCACTCACATGCATGAACACACACACACACACACACATACTGCCTGTGACTTGCTCTCAGGCATCTCTTCCCTGAGTGGAATGAGAAGGTGCATATATTGAGCACCCCTCTGCACAAAGCCATGATTAGGCTCCATGGAGAACAATTACGATACACACAGCACTGTCCTGGGAAGACAGGAGGCAGGGATGGAGAAACTCCCCTGGAAAGAATTAGGCAGGCTGGGTGGCAGACCTCTTCCTGCATCGTGGGACACTGCCTAACTGCACATTGCTGTCCAAGCCCCACCTCTCAGCGCAGAGCCACCCATGACACGGTAACTACTCCTGGTGCCCCTTACTCACCACAACCCACCCTGCACCCCGAGAGACTCAGAACAAGCAGGCGGTTTCCATTTCTGTGAGGGATGAGGAAGACCGAAGGGGCAGGATTTGAGTTCAGAGGGAGATCCCGGTGAGCATCCCACACACACCCTCTCCACTCTGGCCCGGTGTCACCGACCCAGAAAGACATGTCAGTATCCCTCTGCCTTTCCTCTACCTAG
Seq C2 exon
GATGGTTGTCTACAGTGGACGGACAAACACGTCAGCCCTCTTGTACGACTCACTCCGAACAGAGAGCGTGCCCTTCGAGGGCCTGCTGAGCGAGGGTAGCAATATCCGCATCGAGTTCACCTCTGACCAGGGCCAGGCAGCCTCCGCCTTCAACATTCGCTTTGAGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000025612:ENSRNOT00000032193:6
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.098 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF0043115=CUB=PU(49.1=94.6)
A:
NA
C2:
PF0043115=CUB=PD(50.0=94.7)


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:
GTGGAGGAGCAGTGCACAATG
R:
CTCAAAGCGAATGTTGAAGGCG
Band lengths:
326-1878
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]