Special

RnoEX0035992 @ rn6

Exon Skipping

Gene
Description
formin homology 2 domain containing 1 [Source:RGD Symbol;Acc:1589776]
Coordinates
chr19:37293619-37294537:-
Coord C1 exon
chr19:37294431-37294537
Coord A exon
chr19:37294005-37294069
Coord C2 exon
chr19:37293619-37293686
Length
65 bp
Sequences
Splice sites
3' ss Seq
CAGCAGCTACTTGCTTTTAGCAA
3' ss Score
1.32
5' ss Seq
TGGGTAAGT
5' ss Score
10.24
Exon sequences
Seq C1 exon
CTGGAGGACTGTGCGTTGCAAGTGTCGCCCTCTGGATACTACCTGGACCCGGAGCTGTCCCTAGAAGAACAGCGGGAGATGCTGGAGGGCTTCTATGAAGAGATCAG
Seq A exon
CAAAGGGCGGAAGCCCACATTGATCCTGCGGACCCAGCTCTCTGTGAGGGTCAATGCTATCTTGG
Seq C2 exon
AAAAGCTGTATGGCTCCAGTGGCCCCGAGCTCCGCCGATCCCTCTTTTCATTAAAGCAGATATTCCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000054625-'2-8,'2-5,4-8
Average complexity
S
Mappability confidence:
100%=100=100%
Protein Impact

ORF disruption upon sequence exclusion

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

C1:
NO
A:
NO
C2:
NO


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Primers PCR
Suggestions for RT-PCR validation
F:
CTGGAGGACTGTGCGTTGC
R:
TCTGCTTTAATGAAAAGAGGGATCGG
Band lengths:
167-232
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]