Special

GgaINT0027388 @ galGal4

Intron Retention

Gene
Description
multiple EGF-like-domains 11 [Source:HGNC Symbol;Acc:HGNC:29635]
Coordinates
chr10:17688409-17691034:-
Coord C1 exon
chr10:17690906-17691034
Coord A exon
chr10:17688538-17690905
Coord C2 exon
chr10:17688409-17688537
Length
2368 bp
Sequences
Splice sites
5' ss Seq
AAAGTAAGT
5' ss Score
9.72
3' ss Seq
TCTTTTCTTTGGCTCCCCAGAGT
3' ss Score
8.88
Exon sequences
Seq C1 exon
GTTGCCCAGCTGCTTTCTATGGAAAAAACTGTGCCAACGTCTGTCAGTGTCAGAACGGAGCGGACTGTGACCACATCACTGGGCAGTGCACGTGCAGGACGGGATTCACAGGCAAACAGTGCGAGCAAA
Seq A exon
GTAAGTAGCAGCATGACTTCGTTTTCCCATTTCTGGTGGGGAGGAGATCAGAATCCTTTGCAAAAATGAGCTGTGGGCTGAGGTGTGCATGTCTGTCAGCCTCCAGCCCCAGGCACCTTGCGTCATCTGTAGGGAAAAGATGGCATCTCTGGAAAGCCGGCTGGTCTGTTTTAGGGCATAAAGTATGGTGACTCCACTGGAGACTGGGCCTTTCCTTTCCCAGCATGAAGTTAGGTGAGATCAAAGCCTGTCTCACAGCCAGCACTGAATGGAGGCAGCCTTCCCAAACCACTTCACTTGCACCTTATTGATAGGAACCCTAAACCTTACTAAGTCATGCCTTACTAACACTGTTGAGGGCAACAGCATCGGGTTTCCTCAGGCGTGAAGGAAGACAGAAGAGTTCAAAAAGAGTCATTCCACTCTCTGACTTCCAAGGAATATTGAGGTTTCCATGACAAAGTTGTTACACTATAGATGTGGACCAAATAAGGATTCATCTGTACATTGAAAACAGATCAAGGAAACAAAAGCTTCTTGTCATTTTTGGAAGGATTGCAGTTAACTTGAGTAGTGAGCAAGTGTTTAACAATGAACTTCAATTACCTTGCAAGGGTGCTCGCATATCTTACTGTAATTGTTGTCAGCGTCTTGCTGGCATATTTAGCACACTGTGCCAAATGGCTTCTTTTAAGGACAAAGATTTAGGGCTGTGGAAACTGTATATGCTGCAGCTGAAAAATTACTTGTTTGTCCAGTATGGTAAATCAAAAGAAAATTCTCACGCACTTACTTGGATTCTAAATACAGGGTGAAATCTATCTCACCTTACCAGGGCATTAATTCCGCAGGTATATTTTTTTCTTCTTTTTTTGGCAGTAGGTAATGCAATTAAACATTCCTGCTAACTTTGCAAGTCAAAGGCCTACCTCAGAGCTTCCCTGCAGCTTACTGCACAGATCTTTATGAGTGCATTAGAACGTATAACTCAATTCACAAATATCTTTTCCATTTGCACATACTTAACATTCATCCAAGTGTGTGTCTCAGGATCAAATCTGCATGCTCATGGGGATTACGGACAGCACCGCTGTAATTCTGTGAGCAGCCAACTTACTGCGAATTCCTGTGCACCTTTACCCAGGAATAAATAGGAAAGTATGAAGTTTGATAGTAGAGCTGAATCGCAGCAGAAGGTTGTATGCAAGAAACAGTATTTCTAATTTGACCACTCTGCAAAGCCTGTGATTTCATTTTCTATCCAAACTACTAAAGCATTCACTTATTGGCTTTTCTACTATTTAAAAGTATGAAGTGTAATATCTCTGTATTAAGACTCCTTCCTCAGAATCGCACTGGATGGGCAGTTGCACCACATTACAGATGAAATGCCAAAGTGCAAACATCATTTCTGCGGTGCAGTCCAAAAACGTAGGCTCTACTCATTACAGAGACACAGGGTAATGTTCATCACTTCATGTTAACTGGATTGGTAACTGGAATTTGCTCACAGACTGGCACTGGGAAGGTATTGTCACCCTGTGCAAAATCTTTGCAGTGACACTCAAGAAGCCACATGTTCTCCTGAATCATAGCAAGTATGCATACGTTCCGTAATGCCTTCCCTACAGAAATAACAAGGATATGACAGAAGTTGTTTCTTTCAATTTGTTATTGAATGTTGCCTCGAGAAATTTAGTAAGCTGTCTACAGAGTTATCGTAATAGCCCATCATAGTGAGTGTATGAATAAATTTCTCAGTTGGACATTCAATCATTTTGTCTTTGATAGAAATACAAAAACAGGGTAGAAATTCCTACTATGCTGGGAATCCTAATGCAGAAACAGAGCAAATGGAACCGTTCAGATGCTCAGTTCTGTAAGTCCATCTCCAATGTGATATTCTAGCGCTGTTGGGGATAAATATGAAAGCATACAGGATTTGTTTGGTAAAAGTCTGCTGTGTTCATGTGAAAGTACATTAAAACTTCTCTTCGCAGTCTCCCCAGGAAAAGAATGTGCATATGCTATGCTCTTCCAAGATGTTTTCTATAGCCTCTGAGATCATGCCCTGTTAAATCCCGTACGCATGTAATATATATCAAGGCTTTTCAAGTGTGCATGTATTGTTGGTTTCATCCTTGAGAAGTCTTGTATGGCTTTTCCAGAAGGAAAGTTATGGCTTAATACTTTATACCACAAATTGTATACTACATACATCTGTCTCTGGCTTAAAGTAGCAGTGTACCCCTGGGGGGTTATCCTAGTGAAACAAGGGTGACTCTTCTGCTGAATTTCCATGGCGAGGATCTCACCTCCTTCCTCCAGAAAGTCAGGATTCTTTCCAATCTTTTCTTTGGCTCCCCAG
Seq C2 exon
AGTGCTCACCAGGAACATTTGGTTATGGTTGCAAACAACTCTGTGAGTGCATGAATAATGCCACATGTGACCATGTCACAGGTACTTGCTACTGCAGTCCGGGCTTCAAAGGAATCAGATGTGATCAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000007631:ENSGALT00000012349:18
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(69.0=65.9)
A:
NA
C2:
PF0005319=Laminin_EGF=PD(28.6=27.3),PF0005319=Laminin_EGF=PU(78.4=65.9),PF0200911=Rifin_STEVOR=PU(4.9=6.8)


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:
No suggested primer sequences
R:
No suggested primer sequences
Band lengths:
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]