Special

BtaEX6020379 @ bosTau6

Exon Skipping

Gene
Description
Bos taurus integrin, beta 7 (ITGB7), mRNA. [Source:RefSeq mRNA;Acc:NM_001105365]
Coordinates
chr5:26971252-26972271:+
Coord C1 exon
chr5:26971252-26971475
Coord A exon
chr5:26971718-26971937
Coord C2 exon
chr5:26972063-26972271
Length
220 bp
Sequences
Splice sites
3' ss Seq
TCTGTGTGGCCCTACCTCAGGCT
3' ss Score
5.79
5' ss Seq
CAGGTGAGC
5' ss Score
9.6
Exon sequences
Seq C1 exon
CTGTGTCCCCGGCCGCCTGGGTCGACTCTGTGAGTGTTCGGAGGCTGAGCTATCCTCCCCAGATCTGGAGTCTGGGTGCCGGGTCCCCAACGGCACAGGGCCCCTGTGCAGCGGGAGGGGACAATGCCAGTGTGGACGCTGCACCTGCAGTGGACAGAGCTCTGGACGCCTGTGCGAGTGTGACGATGCCAGCTGTGAGCGACATGAAGGCATCCTCTGTGGAG
Seq A exon
GCTTTGGCCGTTGCCAATGTGGAGTGTGTCACTGTCACGCCAACCGCACGGGCAGAGCATGTGAATGCAGTGGTGACACGGACAACTGTGTCAGTCCTGACGGAGGGTTCTGCAATGGGCACGGACACTGCAATTGCGACCGCTGCCAGTGCGACGACGGCTACTATGGTGCCCTTTGTGATCAATGCTCAGGCTGCAAGACACCATGCGAGACACACAG
Seq C2 exon
GGACTGTGCAGAGTGCAAAGCCTTTGGGACTGGTCCCCTGGCCAGGAACTGCAGCACAGCGTGTGCCCACGCCAACATGACTCTGGTTTTGACCCCTACCCTGGATGACAGCTGGTGTAAAGAGAGAACCCAGGACAACCAGCTCTTCTTCTTTCTGGCAGAGGATGAAGCTGGAGGCAGAGTTGTGCTCACAGTGAGACCTCCAGAGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSBTAG00000018993-'17-21,'17-20,18-21=AN
Average complexity
A_S
Mappability confidence:
100%=100=100%
Protein Impact

ORF disruption upon sequence exclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.000 A=0.000 C2=0.056
Domain overlap (PFAM):

C1:
PF079748=EGF_2=PU(32.3=13.2)
A:
PF079748=EGF_2=PD(64.5=27.0),PF079748=EGF_2=WD(100=41.9),PF079657=Integrin_B_tail=PU(5.1=5.4)
C2:
PF079657=Integrin_B_tail=FE(88.6=100)


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Conservation
Chicken
(galGal4)
HIGH PSI
Zebrafish
(danRer10)
HIGH PSI
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
AGTGTTCGGAGGCTGAGCTAT
R:
GTCATCCAGGGTAGGGGTCAA
Band lengths:
301-521
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]