Special

BtaINT0055762 @ bosTau6

Intron Retention

Gene
Description
ELM2 and Myb/SANT-like domain containing 1 [Source:HGNC Symbol;Acc:HGNC:19853]
Coordinates
chr10:85524950-85525584:-
Coord C1 exon
chr10:85525481-85525584
Coord A exon
chr10:85525026-85525480
Coord C2 exon
chr10:85524950-85525025
Length
455 bp
Sequences
Splice sites
5' ss Seq
CTGGTGAGA
5' ss Score
7.54
3' ss Seq
TTTCCTCACTTCCCTTTCAGGAA
3' ss Score
13.47
Exon sequences
Seq C1 exon
TGGAAGACCTGCTGACAGCTGCCTGCTCCAGCATTTTCCCTGGAGCCGGCACCAACCAGGAGCTGGCCCTGCACTGTCTGCACGAGTCCAGGGGAGACATCCTG
Seq A exon
GTGAGACCCTGCTCCCCGGTGGAGGAGGGCCCCTTGGGGAGGCTGGCAGGGAGCTGTGTCTCTGGTCCAGGAGCCAGGCCTGTCAGCGAGCTGATTGGAGGCAGGCGGGAGGGTCTGACCAAGGTGGGGATGGTAGGGGGTCGGCCCAAGGGAGCCCTGGTTCTGGACTCGAGACTTCCCTGTGCAGGGTCCGCTCCAGTCTCTGGGTAGTGGGTCCCCCACCCCTCAGACAGGGCTGTCCACTGAGGACCTTCTCCATCTGTGACTGCCTCCCTTGGGGACCAGGTGTTCTTTCTTGAGACACCCCGAGTGGCCCAACCCCAGTGACCTTGCCCTCCTGCCAGACCTCTTGCCCCTTCGCAGTTAAGAGTTAAGTAATCACCCTACTCAGAGTCCTGGATTTTGGCCACTGAGAACCTGTCAGGGCCCTGACCTTTTCCTCACTTCCCTTTCAG
Seq C2 exon
GAAACGCTGAATAAGCTGCTACTGAAGAAGCCCCTGCGTCCCCATAACCACCCGCTGGCAACTTATCACTACACAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSBTAG00000009272:ENSBTAT00000012216:6
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=0.038
Domain overlap (PFAM):

C1:
PF0144819=ELM2=PD(19.0=31.4)
A:
NA
C2:
NO


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:
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]


SPECIAL DATASETS

  • Pre-implantation embryo development