Special

RnoEX0081951 @ rn6

Exon Skipping

Gene
ENSRNOG00000048853 | Slc25a41
Description
solute carrier family 25, member 41 [Source:RGD Symbol;Acc:1588585]
Coordinates
chr9:10004805-10007662:+
Coord C1 exon
chr9:10004805-10004929
Coord A exon
chr9:10006314-10006469
Coord C2 exon
chr9:10007510-10007662
Length
156 bp
Sequences
Splice sites
3' ss Seq
AGTGGCCGTTGTTCTTGCAGGTT
3' ss Score
10.77
5' ss Seq
CAGGTTTGT
5' ss Score
7.44
Exon sequences
Seq C1 exon
CTGCCCCTAAAATCACAAGGCCAGATAACCAGCCACTCTCAACTGGGAACTGGATAGACGCTCCAGGAAACGCTGAGACTGGGAGCCTAATCCTTCAGGCGGCAACTATGGGAGTCCATCTGGAG
Seq A exon
GTTCTGGACACAGGAGAGCAGCTGATGGTTCCTGGGGATGTCTTGGAAGAGGAAAACAAGGGGACCCTGTGGAAGTTTCTGCTCTCCGGAGCCATGGCTGGGGCAGTGTCTCGCACAGGGACAGCACCTCTGGACAGAGCTAGGGTGTACATGCAG
Seq C2 exon
GTATACTCCTCCAAAAGTAACTTCAGGCACCTGCTGAGTGGCCTGCGGAGCCTGGTCCAGGAGGGCGGTATCCGCTCACTCTGGCGGGGCAATGGTATAAACGTGCTCAAGATCGCCCCGGAGTACGCTATCAAGTTCTCTGTCTTTGAGCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000048853-'3-2,'3-0,6-2
Average complexity
C2
Mappability confidence:
100%=100=100%
Protein Impact

Alternative protein isoforms (Ref)

No structure available
Features
Disorder rate (Iupred):
  C1=0.000 A=0.038 C2=0.000
Domain overlap (PFAM):

C1:
NO
A:
PF0015322=Mito_carr=PU(35.1=63.5)
C2:
PF0015322=Mito_carr=FE(53.2=100)


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
TGCCCCTAAAATCACAAGGCC
R:
GGGCGATCTTGAGCACGTTTA
Band lengths:
242-398
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]