Special

RnoEX0081768 @ rn6

Exon Skipping

Gene
ENSRNOG00000022922 | Slc25a12
Description
solute carrier family 25 member 12 [Source:RGD Symbol;Acc:1305181]
Coordinates
chr3:57898104-57903028:-
Coord C1 exon
chr3:57902947-57903028
Coord A exon
chr3:57901095-57901253
Coord C2 exon
chr3:57898104-57898156
Length
159 bp
Sequences
Splice sites
3' ss Seq
AACTGTTGTTCTGCTTGTAGCTG
3' ss Score
7.06
5' ss Seq
GAGGTGAGT
5' ss Score
10.03
Exon sequences
Seq C1 exon
CAATCCCCCGGCTTGGGCAGACCTATCTGGCTCCAGATTGCCGAGTCTGCATACAGGTTCACTCTGGGCTCAGTGGCAGGAG
Seq A exon
CTGTGGGGGCCACTGCGGTCTATCCCATAGACCTGGTGAAGACCCGGATGCAAAACCAGCGCGGCACAGGCTCTGTGGTCGGGGAGCTGATGTATAAAAACAGCTTTGACTGTTTTAAGAAAGTGTTACGTTATGAGGGTTTCTTTGGACTGTACCGAG
Seq C2 exon
GTCTGATCCCACAGCTGATAGGAGTTGCACCAGAAAAAGCCATTAAGCTAACA
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000022922-'16-25,'16-24,18-25
Average complexity
S
Mappability confidence:
100%=100=100%
Protein Impact

Alternative protein isoforms (Ref)

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

C1:
PF0015322=Mito_carr=PU(14.3=50.0)
A:
PF0015322=Mito_carr=FE(54.1=100)
C2:
PF0015322=Mito_carr=FE(17.3=100)


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Inclusion Isoforms:


Other Skipping Isoforms:
NA
Associated events
Primers PCR
Suggestions for RT-PCR validation
F:
CGGCTTGGGCAGACCTATCT
R:
GCTTAATGGCTTTTTCTGGTGCA
Band lengths:
122-281
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]