Special

GgaINT0124439 @ galGal4

Intron Retention

Gene
Description
notch 1 [Source:HGNC Symbol;Acc:HGNC:7881]
Coordinates
chr17:7828376-7828992:+
Coord C1 exon
chr17:7828376-7828609
Coord A exon
chr17:7828610-7828881
Coord C2 exon
chr17:7828882-7828992
Length
272 bp
Sequences
Splice sites
5' ss Seq
CGGGTAAGC
5' ss Score
9.14
3' ss Seq
CCCCCGCTTTCCTCCTCAAGGGC
3' ss Score
9.09
Exon sequences
Seq C1 exon
GTTTCTCAGGTGTTCACTGTGAGATCGACATCGATGAGTGCAACCCCGACCCGTGCCACTATGGGACCTGCAAGGACAGCATCGCCGCCTTCACCTGCCTCTGCCAGCCCGGCTACACGGGCCACCGCTGCGACATCAACATCAATGAGTGCCAGAGCCAGCCCTGCAGAAACGGGGGGACCTGTCAGGACAGGGACAACGCCTACAACTGTCTGTGCCTCAAGGGGACCACGG
Seq A exon
GTAAGCAATGGGAGCACCTGGGGCGGCGGTGCCGGCAAAGCACCCAGCCTATCCTGGGATGGGTTCACCGTGATGCGCTGCTTTAGGGGATGGCCTGGGGAGGGGGTGTCCTCGGCCGGGGCAGGTTTTCCCAGTTTAGCACCCGCACCTCAGCTGGAAGCTGTCTGCGGGGGAGGCTTTGTTGTGGTGCGGAAGCAGCACCCGTGGGGTTTGTTGTGCATCGTCAGCAGGGCCGGGGGCACCCTGCTAACACCCCCGCTTTCCTCCTCAAG
Seq C2 exon
GGCCCAACTGCGAGATCAACCTGGACGACTGCGCCAGCAACCCCTGCGACTACGGCAAGTGCATCGACAAGATCAACGGCTATGAGTGCACCTGTGAGCCGGGGTACACAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000002375:ENSGALT00000003754:10
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

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

C1:
PF0000822=EGF=PD(16.1=6.3),PF0000822=EGF=WD(100=38.0),PF0000822=EGF=PU(90.3=35.4)
A:
NA
C2:
PF0000822=EGF=PD(6.5=5.3),PF0000822=EGF=PU(93.1=71.1)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
TCGACATCGATGAGTGCAACC
R:
GGTGCACTCATAGCCGTTGAT
Band lengths:
302-574
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]