Special

BtaINT0079948 @ bosTau6

Intron Retention

Description
kielin/chordin-like protein [Source:HGNC Symbol;Acc:HGNC:17585]
Coordinates
chr4:93669410-93670092:-
Coord C1 exon
chr4:93669904-93670092
Coord A exon
chr4:93669581-93669903
Coord C2 exon
chr4:93669410-93669580
Length
323 bp
Sequences
Splice sites
5' ss Seq
ACGGTAACG
5' ss Score
7.77
3' ss Seq
CCTCTCACCTGTCCCACTAGGCT
3' ss Score
9.26
Exon sequences
Seq C1 exon
CTGCCCCCTCGGGCTGCCCCCGGCCAGGGGGCTTGGTCCCTGCCCACCACCAGGAGTACTTCTCCCCGCCCGACGACCCCTGCCGCCGCTGCCTCTGCCTGGACGGCTCGGTGTCCTGCCGGAGACTGCCCTGCCCTCCCGTGCCCTGCACCCACCCGCACCAGGGGCCCTGCTGCCCCTCCTGTGACG
Seq A exon
GTAACGCCCTGGTCATCCCCCTCCCTGCCCTGTCCCCCCTTCTTCCAACTCCACCCCTCGCCTTCTTGGTGCCCCTCTTCCTCCACGCCCCTCTTTATCTCCAGGAGGATGCCACCTCCTCTCCCCACTTCCTCCTGGCCTGCCCCTCCCACATCGGGGTTCTCACTAAGAAAATGGGGAAACAGTGCCCACCTGATCCACAGGGCCTGGCAGGGTGGGGGGTGGTCTCCGGGATGGCTTGGCCTCTAGGGCTGGGAGGGCAGCATGCCCTGGTAATGCGCCTGGTACTCCACGAGCCCCCAGCCTCTCACCTGTCCCACTAG
Seq C2 exon
GCTGCCTGTACCAGGGGAAGGAGTTCACCAGCGGGGAGCGCTTCCCTTCGCCCACTGCCAGATGTCACATCTGCCTCTGCTGGGAGGGCAGCATCAGCTGTGAGCCCAGGGCCTGTGCACCTGCCCAGTGCCCCTTCCCTGCCCAGGGTGACTGCTGCCCTGCCTGTGATG
VastDB Features
Vast-tools module Information
Secondary ID
ENSBTAG00000003449:ENSBTAT00000033567:20
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.016 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF0009313=VWC=WD(100=79.7)
A:
NA
C2:
PF0009313=VWC=WD(100=94.8)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Conservation
Human
(hg38)
No conservation detected
Chicken
(galGal4)
No conservation detected
Chicken
(galGal3)
No conservation detected
Zebrafish
(danRer10)
No conservation detected
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
CAGGGGGCTTGGTCCCTG
R:
CATCACAGGCAGGGCAGC
Band lengths:
336-659
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]