Special

BtaINT0091703 @ bosTau6

Intron Retention

Gene
Description
multiple EGF-like-domains 6 [Source:HGNC Symbol;Acc:HGNC:3232]
Coordinates
chr16:50797838-50798348:+
Coord C1 exon
chr16:50797838-50797966
Coord A exon
chr16:50797967-50798219
Coord C2 exon
chr16:50798220-50798348
Length
253 bp
Sequences
Splice sites
5' ss Seq
AGGGTGAGT
5' ss Score
9.25
3' ss Seq
CACCCGCCCCGTCTCTGCAGAGT
3' ss Score
10.41
Exon sequences
Seq C1 exon
CCTGCCCAGAGGGCCTCTATGGTGAGGACTGTCAGCACTCCTGCCTGTGCCAGAATGGGGGCAGCTGTGACCCTGTCTCAGGACACTGCACCTGCCCAGAGGGCTGGGCCGGCCTGGCCTGTGAGAAGG
Seq A exon
GTGAGTGTCAGGCCGGTAGAGGAGAGGCCCTGGGGGTCTGGGGGCACCCAAGGCCACTGCCCTGGCCCCCTCCCTCTGAGGCCCAAGACGGCTGCCTGGCGTTGAGGGGCAGGGCCCTGGGTGTACCCTGTCGTGTCACCACCCCCGGGCACCTATCCTTCCCAAGGACCCAGGATCCGAGGCTCAGGGTGCAGGAAGCATGGGCAGGGCAGGTGTCCCAGGCCCCCAGGCATCACCCGCCCCGTCTCTGCAG
Seq C2 exon
AGTGCCTCCCGGGGGTCTTTGAAGTTGGCTGCCCGCACAGCTGCGGGTGCCTCAACGGTGGCCTCTGTGATCCGCACACCGTCCACTGCCTCTGCCCAGCCGGCTGGACCGGGGACAAGTGCCAGAGCT
VastDB Features
Vast-tools module Information
Secondary ID
ENSBTAG00000020839:ENSBTAT00000027771:25
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:
NO
A:
NA
C2:
PF126612=hEGF=WD(100=29.5)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Primers PCR
Suggestions for RT-PCR validation
F:
CCAGAGGGCCTCTATGGTGAG
R:
AGCTCTGGCACTTGTCCCC
Band lengths:
253-506
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Pre-implantation embryo development