Special

GgaINT0027376 @ galGal4

Intron Retention

Gene
Description
multiple EGF-like-domains 11 [Source:HGNC Symbol;Acc:HGNC:29635]
Coordinates
chr10:17752703-17754294:-
Coord C1 exon
chr10:17754048-17754294
Coord A exon
chr10:17752824-17754047
Coord C2 exon
chr10:17752703-17752823
Length
1224 bp
Sequences
Splice sites
5' ss Seq
GTTGTAAGT
5' ss Score
8.3
3' ss Seq
TTTCTTCTCTCTCCACAAAGCTG
3' ss Score
8.24
Exon sequences
Seq C1 exon
GTTGCGATAGCGATCACTGGGGACCGCACTGCAGCAACCGGTGCCAGTGCCAGAACGAAGCCCTCTGCAACCCCATCACGGGCGCCTGTGTCTGCGCAGACGGGTACCAAGGCTGGCGCTGCGAGGAGCTCTGTGAGCCCGGGAGCTACGGCAAGGGCTGCCAGTTCCAGTGCCAGTGTCACAACGGGGCGACCTGCGACCACGAGACGGGAGAATGTCACTGCGCTCCTGGATACACGGGGGTGTT
Seq A exon
GTAAGTTCAGTGATGGGTGTACTTCACCCTGCATTGTTTTAACAGCTTTGCTTTGGCTGCTATTAATGCGATGAGTAATTATCAGAATTTGCACTATCTGTATATTATGCACTTTCCTTTGCAGAAATCAGGTAACAGAATTTCAGAGAGGCTGAATAAAGGAAATCTCTGTTATTTGCTGCTAATGATACCTGTCTGCATACCAAAATAGATCTTACTGCTAAAATGAACTCAAAACTCCATGACATTTCCCAACAACTGTGGCTACAACAGCTGTAGCTGTTCCTAATTTCAGTGTGTGAGTACAATCCAAATTGCAGTTCAGTTTTTTTAAGCGGTTGGGCATCCTGCTCGTTAGCAATCCAGTGCAGCATCAAATGGGACTTACCATCCCCAGTTTATTTGGCTTTCTATCTAGCAGAGGAAGCATTACTGGTAACTATATGAGCTTACTATCTAGGGGGTAAATTTTCAGCGTAGTGAGGAGGGATTTAGCGGTGTGATTCCTATTAACTTTAACGAGAATCGTGTAGCTAAATCCCCAAATACCACACAAAGTTTACCAGTAGGATTCACAAAATCTGCATATTAATTTTAGGACAGCAAGAAATAGTTCCTTGTTTAAAATTGCCCACGGTGTAACATCAGTACTCATTAGAGATCTTTCAGTAGTTTCAGAAGTAATTATGCTTTTCAGAATTATTTAAAGGGAAAAGATAATTTACTCACTGAATTTGGCTGGAGATCTATTACAGGTGACTTAATATTTCTGCAGTCTAATAATAGTTGTTGGCCCGCGTGAAGAAGGTAAAAAATAAAGGCAATATTAACCCTCATAAATAAGTGATATACTTTTTGAATATTTTATTTAGTACCTGATTTCCTCATAGCCTTCTGACCTCAGTCCTGAAAGCACTCACTGCTAAATGTTCCGCATGCTATTAGGACTGGTCCCATTGACATTAGCATGTCTGTGCTCAGCAGGAAGTACTTGTATGAACATCCTCATCAGAGAACAGCCACATACTGGGAAAACGTAGAGTACTGTCGGGGATATGAGAGTTGTCTTATTGAAATAGGTGGAATTTGGTGTATGCATAACGATTGCACACATGCATCAGCCTTACAGCATCAGACCTGCGTTGTGGATTTTCCTCTTTTACCGTTTCCTGCAAGTTCTTTTAAATGACCCCGTTGGTTTTTGTTTCTTCTCTCTCCACAAAG
Seq C2 exon
CTGTGAAGAGCGCTGTCCCTCCGGGAGCCACGGAGCTCAGTGTGAGCTGCGCTGCCCGTGCCAGAATGGAGGGGTCTGCCACCACATCACTGGGGAGTGCTCCTGCCCTGCTGGATGGACG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000007631:ENSGALT00000012349:6
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=53.0),PF126612=hEGF=PU(84.6=13.3)
A:
NA
C2:
PF126612=hEGF=PD(7.7=2.4),PF0005319=Laminin_EGF=PU(52.3=56.1)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GATAGCGATCACTGGGGACCG
R:
ATCCAGCAGGGCAGGAGC
Band lengths:
358-1582
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]