Special

RnoEX6044654 @ rn6

Exon Skipping

Gene
Description
hemicentin 1 [Source:RGD Symbol;Acc:1564772]
Coordinates
chr13:67944607-67945939:-
Coord C1 exon
chr13:67945769-67945939
Coord A exon
chr13:67945244-67945414
Coord C2 exon
chr13:67944607-67944777
Length
171 bp
Sequences
Splice sites
3' ss Seq
CACGTTTTCTGTTAATCCAGTGG
3' ss Score
4.15
5' ss Seq
CAAGTGAGT
5' ss Score
9.1
Exon sequences
Seq C1 exon
TCCATGGTGTGTGGAATGCTTGGCAACCTTGGGGTTCGTGCAGCAAAAGCTGTGGAAAAGGCAGTCAGACAAGAACAAGACTTTGCAACAGCCCGCCACCGTCATTTGGTGGGGCCTACTGCAATGGAGCAGAAACCCAGATGCAAGTCTGCAATGAGAGACACTGTCCAG
Seq A exon
TGGATGGCAAGTGGGCAGCTTGGACCAGTTGGAGTACCTGCACTGTATCCTGTGGAGGAGGTACCAGGAAGAGAACAAGGGACTGTTCTGACCCAGTGCCACAGTATGGAGGAAACAAATGCGAAGGGACTGGTGTCCAGAGTGACTTTTGCAATAGTGACCCTTGTCCAA
Seq C2 exon
CCCATGGCAACTGGAGCCCTTGGAGTGGCTGGGGGATGTGCAGTCGGACATGCAATGGAGGGCAGATGAGACGGTACCGCACATGTGATAATCCACGGCCCTCCAATGGAGGAAGAGCCTGTGGGGGTCCAGATACCCAGATCCAGAGGTGTAATACTGACATGTGTCCTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000028627-'107-107,'107-106,108-107=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=0.052
Domain overlap (PFAM):

C1:
PF0009014=TSP_1=WD(100=87.9)
A:
PF0009014=TSP_1=WD(100=87.9)
C2:
PF0009014=TSP_1=WD(100=87.9)


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:
TGTGGAATGCTTGGCAACCTT
R:
CATGTGCGGTACCGTCTCATC
Band lengths:
247-418
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]