Special

BtaINT0097386 @ bosTau6

Intron Retention

Gene
Description
myosin, heavy chain 7B, cardiac muscle, beta [Source:HGNC Symbol;Acc:HGNC:15906]
Coordinates
chr13:64891342-64892729:+
Coord C1 exon
chr13:64891342-64891369
Coord A exon
chr13:64891370-64892632
Coord C2 exon
chr13:64892633-64892729
Length
1263 bp
Sequences
Splice sites
5' ss Seq
CACGTGAGT
5' ss Score
9.3
3' ss Seq
TCATGTTTGTGTCGTCCAAGGGG
3' ss Score
4.26
Exon sequences
Seq C1 exon
ACCGAGAGAACCAGTCCATGCTGATCAC
Seq A exon
GTGAGTGTGGGGCTCTGGGGATGGGGTGGGAAATGCTGGCCATCTGGCAGGAAGGGATTGGAACTAAAATCATTTCCCGAGATTGAATAATTGAATACAAAGTGCTAAAGGCAGGGGTTTTACCACCTAGAGCCAGTGTCCCAGGTGAGGCTAAATTATAGCGTCTTCTCTGCCCCTGTTCTGAGCAGATAAGTAGAAAAGGAATGCCAGACTGATCACCCACCCTCATACCCCCTGTTCCTAGGGCCTGGAATCTTCTCTAACCTTGATCTTTGGGGAGTTCTGATTCTGGCTCAAGGAGGGGGGAGGAGATCCCCTTCCCTTTCCTCTTTATTTTAGTCGGTCAGTCATGTCTGACTTTGAGACCCCATGGACTGTAGCCCATCACACTCCTCAGTCCACGGGATTTCCCAGGCAAGAATACTAGAGTGGGTTGCCATTTCCTCCTGCAGGAGATTTTCCTGACCCAGGGATTGAACCCATATCTCTTGCATTGCACGAGTCTTCTTTACCACTGAGCCACCAAGAAAGCCCTTCTTCTTTATTACCAGCTTCTTATTTCTGAATCTTATTTATAACCCTTTGTTTGCCTCCTTGGGAAAGTGGTAGAATTCTCACATACCAAGTTTAGGTCCAGCCAAGCCAATATGGACATCGGTTGTGCGTGAGTGTGTGTATGTGTGTGAGCGTGCAGCCTGTTGGTTAAGAGTAAAGCCTTTGAAACCAGAAAGACCTGGATTCAAGTTCTCATGGGTCCACTTCCTGCTGGTGCCCTTGGTCCTCTGAATCTCATCAGTAAAAACAGGACAGTCCTGCTCACCTACTGCAGAGCTATAGGAGTCAGCCGGTGAATGTTTGCACCTGGCACCCAGCAGAAACAGCTACATGACCTCTCTGAGTCACATCCCCTTCTCTATCAAGAGGGTGATGATGGCGCCTGCCTTACAGGGTTCCTGAGGCTTCAGTGAACCAGTTCAGGTGAAGCACTCGGCCCAGGGCCTGGCAGTAAGTTAGCGCTCAGTAAACAGTGGCATCATGTGTTTTCTCATCTCACTGGGATGATTTATGCTGGTTTGTTTTGTAAACAATTCAACACCTCTGGGAGCTGACCCATCTCTGAGGAGTTTTGGGTTGGGGGGCTCCTGAGTTGGGAGCTGGGTGTGGGGAGGGCAGAGGCACCCTGCTGGAGAAGTAGGGTGCTGGGGGTGGGAGGAATTAGAGTAGCCAGATGGACATTGGTGATTCATGTTTGTGTCGTCCAAG
Seq C2 exon
GGGAGAATCGGGGGCCGGTAAGACCGTTAACACCAAGCGGGTCATTCAGTACTTTGCCATCGTCGCTGCCCTGGGAGACGGGCCGGGCAAGAAGGCT
VastDB Features
Vast-tools module Information
Secondary ID
ENSBTAG00000003512:ENSBTAT00000039242:5
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.050 A=NA C2=0.121
Domain overlap (PFAM):

C1:
PF0006316=Myosin_head=FE(1.3=100)
A:
NA
C2:
PF0006316=Myosin_head=FE(4.7=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