Special

DreINT0095013 @ danRer10

Intron Retention

Gene
Description
multiple EGF-like-domains 11 [Source:ZFIN;Acc:ZDB-GENE-060503-252]
Coordinates
chr18:19251246-19252538:-
Coord C1 exon
chr18:19252402-19252538
Coord A exon
chr18:19251459-19252401
Coord C2 exon
chr18:19251246-19251458
Length
943 bp
Sequences
Splice sites
5' ss Seq
CAGGTTAAA
5' ss Score
2.54
3' ss Seq
AGTGTGTGAAATGTTTGCAGGTG
3' ss Score
6.09
Exon sequences
Seq C1 exon
GGTTCTGTGTGTGCCCAGCCATGTCCGTTTGGAAAATATGGGATCAACTGCAGCAAGGAATGCTCATGCCGCAATGGAGGACTCTGTGACCACATCACAGGACAGTGTCAGTGCATGGCGGGATACAGCGGCCACAG
Seq A exon
GTTAAACAGATCCCTGATCAGTTATTGATACTCTTTCGTGTCTTTAAAAAAAAAGTGGCACAAAATGCAATGTATGCAAAATGTAGGTACTGAATAATTGATTAATTGCTTTTTTACAACTCAGTGTTTACATTATGTCCACTGATCCCACTCCAAGGTGTGCACTGGTCTGTTAAGTTTCTGCCCATTAATTACCAGTAATAGAGTTTTATTAGGGTCCAATTGAAATTGCTCTTTATTTTCCAGTGTCTTCTGCCGCAGCTTAGGGTTTATTAGCGCGGTAAAGTGATTGTCTGCAGAATGAAAACACTTTCAGGACAGACACTTCTTATCCTCTAATATTTAACAAAATTGCCCTCATTCATTTAGTCTGTGACAGGTGAATTAGCCCAGCAGGAATAATCTCAGATTGCGTTAGTACTGCCGCCTCCCTTACCCCACGTCCTCCTTTCACCCGTCTCTCCTGATACAAACGACACCGGTGTAATTTCAACATGAAACATACCTAGTCCGTTTTATAATTTAATTGAGCTATTTATCTGTCTCCTAATGGCTTCTTTGGACACTGGAGATTGATGTTCTGCCAGGATTGTATATTGAAGATCTCGTGGAAGTCGTTGTTCCTTAAGTCACTTTGCTATTCAACAGAGAGAATGAGCCCGGGTCTAATTGTATTCGCGGTAATTAATGACTGCAGTCTGCGTTTTGCTGTCGTCCCATCTGTGAAGCCAAAGGGGCTGATGAACCTGAGGTACCACAGAAGATGCCCGGAGCTTTGACCCTCGACCCATAGATTAGAAAAGCTCTGTACTATACTAAATCTGCTTGTGCTATTTTGACAGCCTCTTTTTTTCTTTTAAGAATGTATGCTAGTGGTTTCATTGGGGTTTATGGGTAAATAGAGGGGTTTCTTCTTTCTCTGAAGTGTGTGAAATGTTTGCAG
Seq C2 exon
GTGCCAGGAAGAGTGTCCGGTTGGCACCTATGGACCCCAGTGCACCCTCCATTGTGACTGTCAGAATGGGGCAAAGTGTTACCACATCAATGGAGCTTGTTTGTGCGATACGGGATTCAAAGGGCACCACTGCCAGGATAGATTCTGTCCACCAGGCCTTTACGGTCTCATCTGTGACAAATACTGCCCCTGTAATTCCACCAACACAATCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSDARG00000062686:ENSDART00000147902:7
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:
PF126612=hEGF=PD(23.1=6.5),PF126612=hEGF=PU(84.6=23.9)
A:
NA
C2:
PF126612=hEGF=PD(7.7=1.4),PF0005319=Laminin_EGF=PU(18.8=12.5)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GTTCTGTGTGTGCCCAGCC
R:
TGTTGGTGGAATTACAGGGGC
Band lengths:
342-1285
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]