Special

DreINT0094993 @ danRer10

Intron Retention

Gene
Description
multiple EGF-like-domains 10 [Source:ZFIN;Acc:ZDB-GENE-080506-1]
Coordinates
chr10:16150856-16151354:+
Coord C1 exon
chr10:16150856-16151102
Coord A exon
chr10:16151103-16151236
Coord C2 exon
chr10:16151237-16151354
Length
134 bp
Sequences
Splice sites
5' ss Seq
ATTGTAAGT
5' ss Score
8.54
3' ss Seq
GTTTTGGTGTCTCTGTGCAGCTG
3' ss Score
9.22
Exon sequences
Seq C1 exon
CGTGTGACCGTGATCACTGGGGCCCACACTGCAGTAGCCGGTGTCAGTGTAAGAACGAGGCGCTGTGTAACCCCATCACTGGAGCGTGCATATGTGCACCCGGGTACCATGGCTGGCGATGTGAAGACCTCTGTGACCATTCCACTTATGGCAACAATTGCCAACAGAAATGTCTGTGCCAGAATAATGCTACATGCCACCACATCACAGGCGAATGCGTGTGCAGTCCAGGATACACAGGAGCATT
Seq A exon
GTAAGTTTACCTGCATTTTTTTTTGCAAACAATAGAAGATGGTGTTGGAAATACCGTGGCCATGGGAACTAAACCGATACCTTTAATTTAAGTTAGACTGGTAAATGCATAAATGTTTTGGTGTCTCTGTGCAG
Seq C2 exon
CTGTGAGGACTTGTGCCCTCCGGGAAAACATGGACAGCAATGTGAGGAGCGTTGTCCCTGTCAGAACGGTGGTGTGTGTCATCATGTGACTGGAGAATGTTCCTGTCCTGCTGGTTGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSDARG00000017229:ENSDART00000043936:6
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:
PF0005319=Laminin_EGF=WD(100=55.4),PF126612=hEGF=PU(84.6=13.3)
A:
NA
C2:
PF126612=hEGF=PD(7.7=2.5)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Primers PCR
Suggestions for RT-PCR validation
F:
GCTGTGTAACCCCATCACTGG
R:
CACCGTTCTGACAGGGACAAC
Band lengths:
257-391
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]