Special

RnoEX0028498 @ rn6

Exon Skipping

Gene
Description
dynein, axonemal, heavy chain 17 [Source:RGD Symbol;Acc:1563805]
Coordinates
chr10:107092145-107096713:-
Coord C1 exon
chr10:107096557-107096713
Coord A exon
chr10:107095651-107095755
Coord C2 exon
chr10:107092145-107092302
Length
105 bp
Sequences
Splice sites
3' ss Seq
ATCCGCCTTTCCCTTTGTAGTCC
3' ss Score
10.41
5' ss Seq
CAGGTAGGA
5' ss Score
9.79
Exon sequences
Seq C1 exon
GTGCTACATCACACTCACACAGTCCCTCCACCTGATCATGGGCGGAGCCCCTGCAGGCCCTGCTGGCACGGGCAAGACGGAGACAACCAAGGACCTGGGCAGAGCCCTAGGCACCATGGTGTACGTCTTCAACTGCTCTGAGCAGATGGACTACAAG
Seq A exon
TCCTGTGGAAACATCTACAAGGGTCTGGCACAGACAGGAGCCTGGGGTTGCTTTGATGAGTTTAACCGGATCTCAGTGGAGGTCTTGTCTGTGATTGCTGTACAG
Seq C2 exon
GTAAAGTGTGTCCAAGATGCAATTCGGGCCAAGAAAAAGAAGTTTAACTTCCTGGGAGAAATGATAAGTCTCATCCCCACTGTGGGCATCTTCATCACCATGAACCCTGGCTACGCGGGACGCACGGAACTGCCGGAGAACTTGAAGGCTCTATTCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000003028_CASSETTE5
Average complexity
S
Mappability confidence:
100%=100=100%
Protein Impact

Alternative protein isoforms (Ref)

No structure available
Features
Disorder rate (Iupred):
  C1=0.075 A=0.000 C2=0.000
Domain overlap (PFAM):

C1:
PF127742=AAA_6=FE(22.5=100)
A:
PF127742=AAA_6=FE(14.7=100)
C2:
PF127742=AAA_6=FE(22.5=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:
AGTCCCTCCACCTGATCATGG
R:
GCCAGGGTTCATGGTGATGAA
Band lengths:
248-353
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]