Special

RnoINT0132883 @ rn6

Intron Retention

Gene
Description
semaphorin 3F [Source:RGD Symbol;Acc:1308514]
Coordinates
chr8:116443167-116443809:-
Coord C1 exon
chr8:116443721-116443809
Coord A exon
chr8:116443209-116443720
Coord C2 exon
chr8:116443167-116443208
Length
512 bp
Sequences
Splice sites
5' ss Seq
AAGGTAGGT
5' ss Score
10.29
3' ss Seq
TGACCCCTGCTTTCTTCTAGGAG
3' ss Score
10.33
Exon sequences
Seq C1 exon
ACCGCGGGACAGTGCAGAAGGTCATCGTGCTGCCCAAGGATGATCAGGAGGTGGAAGAGCTCATGTTAGAGGAGGTGGAGGTCTTCAAG
Seq A exon
GTAGGTGGTGGAATGCCGCCCAGGCCTGCCCGTGCCTCCTTGACCCTCTCTGGTCCCATCCTTTGACCTTACACTTTTCTTTTTTGAAAAATTTTTTATTAGATATATTTATTTATTTACATTTCAAATGTTAATTCCCTTTCCTGGTTTCCTGTCTGTAAGCCCCCATTCTCTCCCCCCCCATATGGGTATTCTCCCCCCACATTCCCCTACACTGGGGGTCCAAACTTGGAAGACCAAGGGCTTCCCCTTCCACTGGTGCCCCAACAAGACCATCCTCTGCTACATATGCAGCTGGAGCCCTGGGTCAGTTTTTTTTTTTTTTTTTTTTTTGGGTCTTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGTAAGCGCTCTACCACTGAGCCAAATCCCCAACCCCCCTGGGTCAGTTTTGACCTTAGACTTAAGCCGGGGCTGGGAGGGGTCCTGAGCTTCCCCAGGAGCGGATGCTGACCCCTGCTTTCTTCTAG
Seq C2 exon
GAGCCAGCACCTGTTAAAACTATGACCATCTCTTCCAAGAGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000017704:ENSRNOT00000024193:14
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.067 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF0140314=Sema=FE(6.1=100)
A:
NA
C2:
PF0140314=Sema=FE(2.7=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
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]