Special

GgaEX6015421 @ galGal3

Exon Skipping

Gene
ENSGALG00000002375 | Q9W737_CHICK
Description
NA
Coordinates
chr17:8496469-8510458:+
Coord C1 exon
chr17:8496469-8496596
Coord A exon
chr17:8509387-8509649
Coord C2 exon
chr17:8510120-8510458
Length
263 bp
Sequences
Splice sites
3' ss Seq
ATGGCATTTCTCACCCCCAGGTG
3' ss Score
9.99
5' ss Seq
CAGGTGAGG
5' ss Score
10.07
Exon sequences
Seq C1 exon
TGCCCCGGGCTCTGTGCTGTGCCTGACGCTCTCCTTCTGTTCCCAGGTGTGCGGTGCACGCAGCTGGCCGAATCCTGCCTCAACGGGGGCAAGTGTGAAACTTTCCTCAATGGGACGGAGGTGTGCCA
Seq A exon
GTGCAGCAGTGCCCATATGGGCGAGCGGTGCCAGCTGCCCAACCCCTGCCTCAGCTCCCCCTGCAAGAACGCCGGCACCTGCATCCCCCTGCTGCGTGGCAGCACCGCCGACTACACCTGTGTCTGCCGCCTGGGCTTCACCGACGAGCTGTGCCTCACACCCCTGGACAACGCCTGCCTCAACAACCCCTGCCGCAACGGGGGCACCTGTGACCTGGTGACACTCAGCGAGTACAAGTGCCGCTGCCCGCCGGGCTGGTCAG
Seq C2 exon
GTAAAACCTGCCAGCAGGCCGACCCCTGTGCCTCCAACCCCTGTGCCAACGGGGGTCAGTGCGTCCCCTTCGAAGCCCACTACATCTGCCGCTGCACGGCCGGCTTCCACGGGGCCAACTGCAAGCAGGACGTGAACGAATGCAACATCTCACCACCAGTCTGCAAGAACGGTGGCAGCTGCACCAACGAGGTGGGCACCTACCAGTGCTCCTGCAAGCCAGCCTACACCGGGCAGAACTGCGAGCATCTCTATGTGCCCTGCAACCCCTCGCCCTGCCAGAATGGGGGCACGTGCCGCCAAACTGGGGACACCACCTACGACTGCACCTGTCTGCCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000002375-'0-3,'0-2,1-3=AN
Average complexity
A_S
Mappability confidence:
100%=100=100%
Protein Impact

ORF disruption upon sequence exclusion

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

C1:
PF079748=EGF_2=PU(68.6=55.8)
A:
PF079748=EGF_2=PD(28.6=11.2),PF0000822=EGF=WD(100=40.4),PF0000822=EGF=PU(90.6=32.6)
C2:
PF0000822=EGF=PD(6.2=1.8),PF0000822=EGF=WD(100=27.2),PF0764510=EGF_CA=WD(100=36.0),PF0000822=EGF=PU(81.2=22.8)


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
TTTCCTCAATGGGACGGAGGT
R:
TTGCAGGGCACATAGAGATGC
Band lengths:
292-555
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]