Special

DreINT0105518 @ danRer10

Intron Retention

Gene
Description
notch 3 [Source:ZFIN;Acc:ZDB-GENE-000329-5]
Coordinates
chr3:53279646-53280391:-
Coord C1 exon
chr3:53280279-53280391
Coord A exon
chr3:53280176-53280278
Coord C2 exon
chr3:53279646-53280175
Length
103 bp
Sequences
Splice sites
5' ss Seq
CTTGTGAGT
5' ss Score
7.15
3' ss Seq
CATTATCGTCTCTTTTTTAGGGG
3' ss Score
10.06
Exon sequences
Seq C1 exon
GACGAGGGTGTCAAAGTAGATTCAGCGTGTGCGAGTCTCAGCCCTGTAAAAATGGAGGAGTATGTTCCTTGTCTGGCAGCTCCCCACCAGGATACTCTTGCACTTGTCAGCTT
Seq A exon
GTGAGTATCCTGGCTTGAAATGAGATCATTTAACACTATGTTACTACCACTTTCCTCTAGACTTCAAAAGCAGTAACTTAAATCATTATCGTCTCTTTTTTAG
Seq C2 exon
GGGTACGCAGGTTCTAACTGTGAGAGGAGCATGAACTGCAAAGAGCTGCCTTGCTACAATGGAGGCAGTTGCACTCTCACCACACGAGGGGCACGTTGTACTTGCATTCAGGGCTTTGGTGGGCCATTGTGTCAGCACCGCAGCAATGACGGCTGCTCCTCCAAGCCATGCCACAATGGAGGCTTATGTACAGAGGAAACCAGCTATCCATTTTTTCACTGCCAGTGCACCAATGGCTGGAAAGGCAAACGATGTGAACAGAAAACTGGGTCATCGGCTCCACTTCCTTCTCCTTGCCCTATTGCTGACTGCTTCAGCAAGGCCAATGACGGTGTGTGTGACAAAGAATGCAACTCCTTAGACTGCCGCTGGGACGGAGGTGACTGTTCTCTTGCTGTAAACCCCTGGGCACGCTGTGCAGACCCTCGATGCTGGCGGCTCTTCAATAACAGCCAATGTGACGAGTTTTGCAATAACGCAGAGTGCCTGTTCGATAATTTCGACTGCATAAACAAAGAGAAAGTCTGCAA
VastDB Features
Vast-tools module Information
Secondary ID
ENSDARG00000052139:ENSDART00000073930:23
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(6.1=5.3),PF0000822=EGF=PU(79.4=71.1)
A:
NA
C2:
PF0000822=EGF=PD(14.7=2.8),PF0000822=EGF=WD(100=17.5),PF0000822=EGF=WD(100=18.6),PF0006612=Notch=WD(100=20.3),PF0006612=Notch=WD(100=20.9),PF0006612=Notch=PU(15.0=3.4)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Primers PCR
Suggestions for RT-PCR validation
F:
TGCGAGTCTCAGCCCTGTAAA
R:
CTTGGAGGAGCAGCCGTCATT
Band lengths:
249-352
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]