Special

RnoEX6044661 @ rn6

Exon Skipping

Gene
Description
hemicentin 1 [Source:RGD Symbol;Acc:1564772]
Coordinates
chr13:67816643-67819903:-
Coord C1 exon
chr13:67819790-67819903
Coord A exon
chr13:67818933-67819058
Coord C2 exon
chr13:67816643-67816771
Length
126 bp
Sequences
Splice sites
3' ss Seq
ACCTTTATTCTTTTATCAAGATG
3' ss Score
5.71
5' ss Seq
TTGGTGAGT
5' ss Score
9.27
Exon sequences
Seq C1 exon
ATATTAATGAATGTCAGGAATCCAGCCCCTGCCACCAGCGGTGTTTCAATGTCATAGGAAGTTTCCACTGTGGCTGTGAAGCTGGCTATCAACTCAAAGGCAGAAAGTGCATCG
Seq A exon
ATGTGAACGAATGTAGACAGAGCGTGTGCAGACCAGACCAGCACTGTAAGAACACCCGCGGTGGCTACAAGTGCATTGATCTCTGTCCAAGTGGAATGACCAAGGCTGAGAATGGGACCTGCATTG
Seq C2 exon
ACATTGATGAGTGCAAAGATGGGACCCACCAATGCAGATATAACCAAATATGTGAGAACACGAGAGGCAGCTACCGGTGTGCATGCCCAAGGGGTTATCGGTCTCAAGGAGTTGGAAGACCCTGCGTTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000028627-'121-122,'121-121,122-122=AN
Average complexity
A_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:
PF0764510=EGF_CA=WD(100=94.9),PF0764510=EGF_CA=PU(0.1=0.0)
A:
PF0764510=EGF_CA=WD(100=95.3),PF0764510=EGF_CA=PU(0.1=0.0)
C2:
PF0764510=EGF_CA=WD(100=95.5),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:
TATTAATGAATGTCAGGAATCCAGCC
R:
CAACGCAGGGTCTTCCAACTC
Band lengths:
242-368
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]