Special

RnoEX0042106 @ rn6

Exon Skipping

Gene
Description
hemicentin 1 [Source:RGD Symbol;Acc:1564772]
Coordinates
chr13:67819790-67926937:-
Coord C1 exon
chr13:67926818-67926937
Coord A exon
chr13:67926218-67926352
Coord C2 exon
chr13:67819790-67819903
Length
135 bp
Sequences
Splice sites
3' ss Seq
CATGGCTCCCTCTGTTGTAGACA
3' ss Score
8.97
5' ss Seq
AAGGTAGTT
5' ss Score
6.44
Exon sequences
Seq C1 exon
ATGAGGATGAATGCACAGCTGGGAACCCCTGCTCTCATACCTGCCACAATGCCATAGGAGCCTATTATTGCTCCTGTCCCAAAGGCCTCACCATAGCTGCCGATGGGAGAACCTGTCAAG
Seq A exon
ACATTGATGAGTGTGCTTTGGGTGGACATACCTGTCATGCTGGTCAAGACTGTGACAATACCATTGGATCCTATCGCTGTGTGGTCCACTGCGGAACAGGCTTCCGGAGAACCTCTGATGGGCTGAGCTGTCAAG
Seq C2 exon
ATATTAATGAATGTCAGGAATCCAGCCCCTGCCACCAGCGGTGTTTCAATGTCATAGGAAGTTTCCACTGTGGCTGTGAAGCTGGCTATCAACTCAAAGGCAGAAAGTGCATCG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000028627-'118-119,'118-117,120-119
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:
PF146701=FXa_inhibition=WD(100=90.2),PF0764510=EGF_CA=PU(0.1=0.0)
A:
PF0764510=EGF_CA=WD(100=95.7),PF0764510=EGF_CA=PU(0.1=0.0)
C2:
PF0764510=EGF_CA=WD(100=94.9),PF0764510=EGF_CA=PU(0.1=0.0)


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Inclusion Isoforms:


Other Skipping Isoforms:
NA
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
ATGAGGATGAATGCACAGCTGG
R:
CGATGCACTTTCTGCCTTTGA
Band lengths:
234-369
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]