Special

BtaINT0011129 @ bosTau6

Intron Retention

Gene
Description
ATP-binding cassette, sub-family A (ABC1), member 5 [Source:HGNC Symbol;Acc:HGNC:35]
Coordinates
chr19:61917540-61918177:+
Coord C1 exon
chr19:61917540-61917715
Coord A exon
chr19:61917716-61918101
Coord C2 exon
chr19:61918102-61918177
Length
386 bp
Sequences
Splice sites
5' ss Seq
TCGGTAAGG
5' ss Score
10.48
3' ss Seq
TCATGCCATCTCTTTTGCAGAAT
3' ss Score
9.9
Exon sequences
Seq C1 exon
GTCTTCCTAGGAGACTACTCTCCACACCCAGCTGAAGACGACGACTCCGTGAGGTGTATGGGCTACTGTCCCCAGATCAACCCCCTGTGGCGAGACATCACCCTGCAGGAGCACCTCCAGATCTATGGAGCTGTGAAAGGGATGAGAGCCAGTGATGTGCAGGAGGTCACAGATCG
Seq A exon
GTAAGGCCCCGCCTTCAGCACCCCCTGTCACCTGCGGAAGGTCATGACACACAGTTTCAAAATTTCACAACAGGCATTTCCCTGGATCATAGTTTTTCATGGAAAAAGATCATTACTTTTCCATATATTCTTTTACCAACTTATGACAGCTATGAAAATGAAAACACTTACATTTCTGAATACAGAATAAATGTACTTATGAATTGCCATGAAACGTATTTTAATTTAAAGCGAAACTTTTAGTCATGATGTTGATTTATTTGAAGTGAGCTTCCACCAACTTATCTGTTTTAGGAAGAAAAAACAGCCTCAGGGACCACAGTCTGTATTATTAATTGTATCTGTGGGTATTGTGGCATGCTCATTTCATGCCATCTCTTTTGCAG
Seq C2 exon
AATAACAAATGCACTTGATCTAAAAGAACACCTGCAGAAAACAGTGAAGAAACTTCCTGCAGGAATCAGGCGCAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSBTAG00000002747:ENSBTAT00000003563:31
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.034 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF0000522=ABC_tran=FE(39.7=100)
A:
NA
C2:
PF0000522=ABC_tran=FE(17.1=100)


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:
GACTACTCTCCACACCCAGCT
R:
CTTGCGCCTGATTCCTGCAG
Band lengths:
240-626
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Pre-implantation embryo development