Special

RnoINT0134569 @ rn6

Intron Retention

Gene
Description
SH2 domain containing 3C [Source:RGD Symbol;Acc:1307287]
Coordinates
chr3:11787960-11789571:+
Coord C1 exon
chr3:11787960-11788082
Coord A exon
chr3:11788083-11789455
Coord C2 exon
chr3:11789456-11789571
Length
1373 bp
Sequences
Splice sites
5' ss Seq
CTGGTACGT
5' ss Score
9.57
3' ss Seq
CCCTTTGGGCGTCTTTGCAGGTT
3' ss Score
9.67
Exon sequences
Seq C1 exon
TCCCAGCTGATCCCCAAGGAGAACCGGCCTCTGGAGGTGGGCCTGCTGCGCAAAGTCAAGGAGCTGCTGTCGGAGGTGGATGCCCGGACGCTGGCCCGGCATGTCACCAAGGTTGACTGCCTG
Seq A exon
GTACGTGTTAGGAATGCTTAGGGAGGGGACAATACCTTTAACATCTGGCTTTGAGGTCAGGAGTCAAGATGGTGACGGGCTGATTTCAAAATTCCCCAAGTACAATGACGCCAGCAGCCTGAGTTTTGACATCCCAGGTGTCTCAGGCCCCTTTTTCAGATTTATTTATTTTATGTATGTGAGTGCACTGTCGCTGTCTTCAGACAGACACACCAGAAGAGGGTATCAGATCCCATTACAGATGGTTCTGAGCCACCATGTGTTTGCTGGGAATTGAACCCAGGACCTCTGGAAGAGCAGTCAGTGTTCTTAACCACTGAGCCATCCTTCCAGCCCTCCATTTTCTTATTTTAGATTGTTTTGTTAGGGTCTCACTATGTAGCCTTGGCTGGGCTGGAACTAGCTGTGTAGATGAGGCTGGCTGCTATGTAGACCAGGCTGGCCTTGAACTCATAGAGAGCTTCCTGTCTCTGCCTCCCAAGTGCTGGGATTGAAGGCATGAGCCACCACCCCTTGCCAGTCTCCTCCTCCTTCTCATTTCATTTTTGATGTGCACTGGTGTTTCGCCAGCACGTATGCCAGGACTAGAGTTATAGGCAGTTGTGGACCACCATGTAGTTGCTGAGAATCAAACCTCAGTCCTTTTGGAAGAGCAGCCAGTGCTCCTAACCACTGAGCCATCTCTCCAGCCCAATTTTCTTCTTTGGAAAAGTGACATCCAAGGTATTTCTACAGCCTGCAGATGTTGGTTTAGAATGAGAGATGACGTTTTGGGGGTAACTTAAGGAACATCCTGGTTCTAGTCTATATAAAATGAACATCTGGTTGGGGGGGGCATCTTCTCCCTTGACCCCACATTTCCTAGTGGACAACAAGCAAAACATTCCCTGGCCTCAAAACTGTCCCCATGCCAGTGTGAGGCACTGACTCCGCTAAGAATCACAGCTCTTTGCATACCTCGGTTTCTCTGTAGTTTCATATGAACGCTGCCTGCTGAGAAGAGGGAGGAACTGGGTTGCAGGCTCAAGTGTATGAACTTGAGCAAGAGAGTCCGTTCCCTTCCTGGGCTTTGGGTTGGCAATCAGGATAATGACATCCTGGCTCTTAATCTTGAGTAGTTAACATCGCACACACCTATGGGCATCTGATCTTCCTACTCCCCATTTTACAGATGGGGAAACTGAGGCTCACTCAGAAAGGGGGAAATTGCTACGTGTTCACAGAGGAGCTGGGATTCAACCCCCACCCAACCCTACTCCACCCCACCCTCTGAACCCTATAGCCAGGCGACCCTCTTAGATGAAGCTCTGACTCCCAGATGGCTTGGACCAACCCTGACAGGAAATTAATCAGCCCTTTGGGCGTCTTTGCAG
Seq C2 exon
GTTGCTAGGATACTGGGCGTTACCAAGGAGATGCAGACCCTAATGGGAGTCCGCTGGGGCATGGAGCTGCTCACCCTCCCCCATGGCCGGCAGCTAAGACAAGACCTGCTGGAAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000054560:ENSRNOT00000078366:7
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.683 A=NA C2=0.000
Domain overlap (PFAM):

C1:
NO
A:
NA
C2:
PF0061714=RasGEF=FE(22.5=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
TCCCAGCTGATCCCCAAGG
R:
TTTCCAGCAGGTCTTGTCTTAGC
Band lengths:
238-1611
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]