Special

BtaINT0011141 @ bosTau6

Intron Retention

Gene
Description
ATP-binding cassette, sub-family A (ABC1), member 6 [Source:HGNC Symbol;Acc:HGNC:36]
Coordinates
chr19:62056679-62057363:+
Coord C1 exon
chr19:62056679-62056789
Coord A exon
chr19:62056790-62057187
Coord C2 exon
chr19:62057188-62057363
Length
398 bp
Sequences
Splice sites
5' ss Seq
CAGGTGGGC
5' ss Score
8.07
3' ss Seq
AATTATTTTTAACTTCTTAGGAT
3' ss Score
7.88
Exon sequences
Seq C1 exon
GCTTGTCCTTTGACATCTATGAAGGTCAGATCACGGCAGTCCTGGGTCACAGTGGGGCTGGCAAATCGGCGTTGCTGCGCATCCTTAGTGGGTCGTCTGTTCCAACAGCAG
Seq A exon
GTGGGCAGACGATGCTTCCCAAAGGCACCCGCCTGAGCGCAGAATGAGGCCTTGTGTGCTTTTTTGTTTTCAGGTTGTAATTTAACCGCCTTAGAGGAAGTGATGTTCGTTTATCTAAAGCTGTTTACCAGAACTACATGATTTTATATATATTTTCGATTTCCCAAATTTTCATGAAAATCCTGATCTTCATTTCTGTGTGATATTTCAGGGGAGATATTGTGTATACACTATTCTCAACGTCTGTTTGTGCTGAGAGTAGTTAATGGTTGTTAATAAATTATAAAATCATCATTTTAGATACTTCTGAATATATGCCAATATTTTCCTAAATAAGATCTACAGACATTAATAAAATGTATTATCTCACCAATGTTAAATTATTTTTAACTTCTTAG
Seq C2 exon
GATCAGTTACCATCTATAATAAAAATCTCTCCGAAATGCAAGACTTGGAGGAAATCCGGAAGATAACTGGTGTTTGTCCTCAATTCAATGTTCAGTTTGACACGCTCACTGTAAAGGAGAACCTCAGGCTGTTTGCAAAAATAAAAGGAATTCAGCCAAAGGACGTGGAACAGGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSBTAG00000006921:ENSBTAT00000009089:11
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:
PF0000522=ABC_tran=FE(25.2=100)
A:
NA
C2:
PF0000522=ABC_tran=FE(39.5=100)


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:
TGTCCTTTGACATCTATGAAGGTCA
R:
GTTCCACGTCCTTTGGCTGAA
Band lengths:
279-677
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Pre-implantation embryo development