Special

BtaINT0127963 @ bosTau6

Intron Retention

Gene
Description
retinoid X receptor, alpha [Source:HGNC Symbol;Acc:HGNC:10477]
Coordinates
chr11:106004221-106007781:+
Coord C1 exon
chr11:106004221-106004390
Coord A exon
chr11:106004391-106007651
Coord C2 exon
chr11:106007652-106007781
Length
3261 bp
Sequences
Splice sites
5' ss Seq
TCGGTGAGC
5' ss Score
9.1
3' ss Seq
ACCACGGTGCCCCTCCCCAGCCC
3' ss Score
6.14
Exon sequences
Seq C1 exon
CCGTGCAGGAGGAGCGGCAGCGGGGCAAGGACCGGGGCGAGAGCGAGGTGGAGTCCAGCAGCAGCGCCAACGAGGACATGCCAGTGGAGAAGATCCTGGAGGCCGAGCTGGCCGTCGAGCCCAAGACCGAGACCTACGTGGAGGCGAACGTGGGGCTGAACCCCAGCTCG
Seq A exon
GTGAGCGCCCCCGCCCACGTCCATCTGCTCTGCTCTGGGGACGGAGGCCCTGGGAGCATGCCTGGGAGGGGGCCCTGTCATCACACCCCCGCCTGGAGGGGGACCCTGTCACCCCCCGTGCCCCTGCCCCTCCGTGAGGCTCTGCTGCCAGTCAGGTGGGCGAGTTTTCTATTGTTGGGCTCAAAGCCCAGGACTTTACAGCTCCCTTCCAGCTTCCTGTTACCTCTGGCCCATCGTGCAGCCAGGCCTGTGGGCAGCACTGGGTGTCAGCATGATCTGTGTCTCCCGTGTGGGTTCAGGGCGGCCCTGGGGTCCCCCTGGCTTCTCTCCTCCGTTCTGTCCCTGCCTCACGTGGCCCGGACGCCCCGCCCACTCCTGCCCCAGGGCCCTTGCTCGTGTGGTCTCCACCGTTCCTCCTCCGGCTTCAGCCTTGCCAAGTGTGCCTTCCTTGGGGAGCCCTTTCCCTCTCGACTGCCTTGTTCCCCCTTCATGGGGGCTCGGCGCCCTTGACGCTTGGGGGTCACGGCGCGGCGAGTGTGGTGGTTCGTTCTCCATCCTGGCCGTCGGACGGTCCCCCGTGCCCGGCTGCGGTCAGGGACAGGACCCTGCCGTCCCGTAGGTGCTTGTTCACGGCCCCCCAGTCTCAGAGCGTGGGGGTCGCATCCTGCCTGCAGTCTCAGGACACCCTGCTTCCTTGTCCCCCTGCGACAGAGCGCCCCAGGCTGCAGCCCCTCTCAGACCCCTACGCTGGCTGCCCCGCCGTGTTGCCTCTTGTGTGCAGTGACCACCCCACCCGCCGCCGGTTTGACCCTCGACAGTCCCTCTGGTCTGTGGCCCGACCCCACCCGATGGCTTCTCTAGTCCCAGTGGGGAGCCAGGGTGGCCGCAAGGGCCTCACGATTGAGCAGAAACCCTGAAGGAAAAGTCAGGGGTCTACACCCGTCTGCCAGGTTTTACTCTTGTCCAGTGAGGACACCATCTGGGAGGAAATGAGTCTGCCCTCTGCGCGCTCCGGGAATGCAGAACAGGCGGGCGATTTAGGGGACAGGCCGGTGGGCTGGCTGGTGGGGGCTCTGCCCTCCTGTGGCCGCTCCTGGTGGATTGGCCTGGGTCCCCCTCTGGGGCTGGCTCGTTCAGCCCCTTCCCCCAGACCAGGGACACCTGTCGGCCCCGGGGGAGCCTCAGGTCCCAGCCTGGGGGCCCCGCGGTCCCCTGCTAGGACAGGGAAGGCTCTGCCCTCTCCGGCAAGGGGCCAGAGCTCAGGAAACTGCTGTTGAATGAGGCCTGTTTTGTCTTTTTGTGGGAATGAGGCTCAGAGGATGGAGCCTGGTAGAGTTCAAGCTCCTCCCCCAGGGGAACCCGCTCCCTCCAGGCCAGCCCCGCGCCTCTGGTGCAGGTAACCTTTGCCCCCAGCTTATTAGGTATGACCCGGCACCTGCCTCCGAGGCCCTGGCCTACTCCACTGGGCCTGCTCTGGGCCCCTTGGGGGCTCAGGGGGGGCTCCCGCTAGTGACTAGAGAAGGCCCGACCTCTGGGGCTTCAGCCCAGGACTCGTTGGTCTTCCCCACGCCTTCTGCCCCGCTCAGTGCATCTCCCCGGACCCCCCGCCGTCAAGCTTGGCCTCCCAGCCGTAGGCTGGAAGGGCTCGGAGCAAGGTCCCTGAGGACTGGAGCCTGGCCCCAGGCTCTGGCTCACTAGGTGCTGGATGTGTCGCTCGGGTGAGCCGGGTTCCCGGTGCAGGCTAGCTCTGCTCGTGGCTGTGGTCATCTGGCGGCCGGGATGGGTGTGCAATGCCCAGAGGGTGTGCTGGGCTTGGGCACGTGGAGTCTGGGCGCCCCGAGTGCTGGGCTTCTGGTCACTGCTCCTGGGTGGAGGCGGGAATGCTGTGGGGCTGGCCCCCTGGGGCCTCGGTGTGACGGTGACTCTGGGGGCGTCTGGGCACTGGCACCTTCCACCCACTTCCCCTGACTGGCCGTATGGCCTGGAAGCCGCTTCTCCCACGGCCCCAGGTACTCCTTCTGCACGCCGGCCCCCATGCCCCTCTGTCACAGACCTCCCAAGAGAGCCCTCAGCAGGCCCTTCACGGCCGGATTGTTTAGACTGCGCGCCACGGGAGGGCACATGGTTTCTATCAGGGAAGCTCCTCCAGGCTCCCCACGCCGTCGGGGGTGGGGGGGATGCCTGGCCCAGGTGGTTCCTGGAATGAAGCGCTTACGCTTCCGCTGCCTGGGCCCCACCCCCCAGGGCCTGGCGAGTTCTCCGTCGGAGCCCCGTGGGCTGGAGCCTGCAGCCACTGAGGCTGCCCGGGTTCCCCCGTTTGTGAGGATGACTGGGTGTCCCCTTCTGGCTAGGGGCTTCCCAGGTGGCTTAGTGGTAATGAATCCGCCTGCACTGCAGAAGACAACGGGTTCGATCCCTGGGTCAGAAAGATGCCCTGGAGGAGGAAATGGCAACCCACTCCAGTGTTCTTGCCTGGAGAATCCCACGGACAGAAGAGCCTGGTGGGCTACAGCCCATGGGGTCTCAAGAGTCAGACACGACTACATGACTGAGCACGTACGCACGCCCCTTCTGACCAGAACTTTCCGGAAGGGCTTCGGGTGCACCCTTGTGTGTTGCCACGTCCAAATTTGGGAGGAAGCACCACCACCAGAGGGGCTGGCACTGCCCATGCCCTCCCCATGCCTGGTCCGCAACACGAGGTCACCTGGCATCGGCCCAAGGGCCGCGGTGGAGACCGAATGGGTCATGGCACGGTGACCTTTCTGTGGCTGCTGGACAAGTGACAGCAAACTGAGGGCCTAAAGCAGCACAGATCTCACTGCCTCACGCCCCTCGAGGCGAAGCCTGAGACCTGCGCCCCTGGGCCAAGTCAGGGCGCCGGCAGGGCTGGCCCTCGCAGGCGTGCGGGTGGGGGCCGCGCCCGGCCTCCGCTCTGGAGGCGCCCCGGGCCCCGGCTCCGGCCCTTCTTCCAAGTCTGCCGGCAGCTCTTCCCTCCTTGACCTTGGCCTCGGCCCTCGTGTCCTCCCCCCCAGCAGGCGCTCTGTGATGACCCCGGGCCCACCCACACCTTCCAGGGTCACCTCCCATCAGAACCCTTCACTCAGCCGTGCTCGCCGATTCCTTTGTGCTGGGGTTCGGGGGCTGAGGTCGTGGGGGTCGTGGGGGCGTCGGTCAGCCCCCGCTGCTGCGTCGGGCGTGTGGGGGCCTGATCAGGGGCTCTGTTCAATGCACGGTGCTCACCACGGTGCCCCTCCCCAG
Seq C2 exon
CCCAACGACCCCGTCACCAACATCTGCCAAGCGGCTGACAAGCAGCTCTTCACACTGGTGGAGTGGGCCAAGCGGATCCCGCACTTCTCCGAGCTGCCCCTGGACGACCAGGTCATCCTGCTGCGAGCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSBTAG00000017851:ENSBTAT00000023729:4
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.544 A=NA C2=0.068
Domain overlap (PFAM):

C1:
PF0010425=Hormone_recep=PU(2.1=7.0)
A:
NA
C2:
PF0010425=Hormone_recep=FE(23.0=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:
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