Special

DreINT0014414 @ danRer10

Intron Retention

Gene
ENSDARG00000074808 | MEGF6 (1 of 2)
Description
multiple EGF-like-domains 6 [Source:HGNC Symbol;Acc:HGNC:3232]
Coordinates
chr11:41117148-41117816:-
Coord C1 exon
chr11:41117688-41117816
Coord A exon
chr11:41117277-41117687
Coord C2 exon
chr11:41117148-41117276
Length
411 bp
Sequences
Splice sites
5' ss Seq
AAGGTCAGC
5' ss Score
7.09
3' ss Seq
TGTGTGTGTGTGTGTTGTAGCAT
3' ss Score
10.23
Exon sequences
Seq C1 exon
AGTGTGAACGGGGCTGGTTTGGCGTGGGTTGTGAGGACCGCTGTCAGTGTGATCACGGTGCTGTCTGCCATCACGTGAGCGGTCAGTGTCTCTGCCCTGCTGGATGGAGAGGAAGACGCTGTGAGAAAG
Seq A exon
GTCAGCTCATTAAAAAAAATCAAATATATATAATAAATGACTTTATAAATATTATTACTAGAATATATTTCACCCATAATGAATAGTTAAATGTCATTAAATAATACATAATTTAAATTTCTTTAAATATTTATTTATTAATTATACATGTATTATGTTTGAAATGACATTAATTATATACGAGCAATTATTAAATATTTAATATATGTGAAACTGTACCTTTATTTGAAGTGTGTGTAACATATGTTGTGTCTCTGCATGTTGTGTGTGTGTGCATGTGTCGTGTGTCTCTGTGTGTGTCTGTCTGGGTGTGTAATGTGTGTGTGTGTGTGTTTCTCTCTCTCTGTTGTCTCTTTCTTTCTCTCTGTCTCTCTCTCTTTCTCTGTGTGTGTGTGTGTGTGTGTGTTGTAG
Seq C2 exon
CATGTCTGCCGGGCTCATTTGGTCAGGATTGTGTCCAGCGCTGCTCTTGTCCGTCCGGCTCCTCGTGTCATCATGTGACCGGTCACTGTGGTTGTGCTCCAGGATTCACCGGCGACGGCTGTGAACACA
VastDB Features
Vast-tools module Information
Secondary ID
ENSDARG00000074808:ENSDART00000109204:28
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=PU(63.0=65.9)
A:
NA
C2:
PF0005319=Laminin_EGF=PD(34.8=36.4)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GTGTGAACGGGGCTGGTTTG
R:
TGTGTTCACAGCCGTCGC
Band lengths:
257-668
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]