Special

BtaINT0091693 @ bosTau6

Intron Retention

Gene
Description
multiple EGF-like-domains 6 [Source:HGNC Symbol;Acc:HGNC:3232]
Coordinates
chr16:50791566-50792276:+
Coord C1 exon
chr16:50791566-50791700
Coord A exon
chr16:50791701-50792141
Coord C2 exon
chr16:50792142-50792276
Length
441 bp
Sequences
Splice sites
5' ss Seq
ATGGTGAGT
5' ss Score
10.13
3' ss Seq
TTTCCCCTCTCCCTCTGCAGAGT
3' ss Score
13.75
Exon sequences
Seq C1 exon
CCTGCCCGCCATGGGCCTTTGGGCCAGGCTGCTCAGAGGAGTGCAAGTGTGAGCAGCAGAATACGCGTGCGTGCGATAAGAGGGATGGCAGCTGTGCCTGCAAGGCGGGCTTCAGGGGCGAGTGGTGCCAGGATG
Seq A exon
GTGAGTACAGGGCCGGGGGGAGGAAGAGGGCCCCAGGGGAGGGGGACAGGCCCCAGGGGAGGGTGAGCAGGTCCCAAGGGAGAGGGACAGGCCCCAGCAGAGGGGGACAGGCCCCAGGGGAGGGGGAAAGGCCCCAGGGGAGAGGGACAGGCCAGGGGAGGGGGGACAGGCCCTAGGGGAGAGGGACAGGCCCCAGGGGAGAGGGACAGGCCCCAGGGGAGGGCGGACAGGTCCCAGGGGAGAGGAACAGGCCCCAGGGGAGAGGGACAGGCCCCAGGGAATGGGGACAGGCCCCAGGGGAGGGGGAAAGGCCCCAGGGGAGAGGGACAGGCCAGGGGAGGGCGGGCAGGTCCCAGGGGAGAGGGACAGGCCTCAAGGGAGGGGGGACAGGCTCCAGGGCCCTTGGAACCTTGCAGACGCCTTTCCCCTCTCCCTCTGCAG
Seq C2 exon
AGTGCCAGCCGGGCTTTTTTGGGCCAGGGTGCCGGCAGGCGTGCACCTGCCCCCCGGGCGTGGCCTGCGACCCTGTCAGTGGCGAGTGTGGGAAGCAGTGTCCCGCTGGCTACCACGGGGAGGACTGCGGCCAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSBTAG00000020839:ENSBTAT00000027771:16
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(64.6=67.4)
A:
NA
C2:
PF0005319=Laminin_EGF=PD(33.3=34.8)


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:
CTTTGGGCCAGGCTGCTC
R:
CTTGGCCGCAGTCCTCCC
Band lengths:
254-695
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Pre-implantation embryo development