Special

BtaINT0079635 @ bosTau6

Intron Retention

Gene
Description
potassium channel, voltage gated eag related subfamily H, member 8 [Source:HGNC Symbol;Acc:HGNC:18864]
Coordinates
chr1:138582405-138583713:+
Coord C1 exon
chr1:138582405-138582604
Coord A exon
chr1:138582605-138583463
Coord C2 exon
chr1:138583464-138583713
Length
859 bp
Sequences
Splice sites
5' ss Seq
GAGGTAATG
5' ss Score
8.73
3' ss Seq
TCTTTCATCTTCTCTGGCAGCTT
3' ss Score
9.4
Exon sequences
Seq C1 exon
CCTTGATGCACGCCCTGGTGTTCGGAAACGTGACAGCGATCATCCAGAGGATGTACTCCAGGTGGTCCCTCTATCACAGCAGAACCAAGGATCTGAAGGACTTCATCCGTGTCCATCACCTGCCCCAGCAGCTCAAGCAGAGGATGCTGGAGTATTTCCAGACAACCTGGTCAGTCAACAATGGAATAGATTCCAATGAG
Seq A exon
GTAATGTGAATTTCTCCTGTTGACGTTTTCAGGCAGAAAGCACGTATTCTAAGGTAAAAGCAAGCGCTTTAGTGCAGGTCTAAGAAGTGAAGCACACACCTACCAACTTCTTTATCTCTTTGCGTTTAGCCTCTCATGACCCCCGCAGGGGTTCTTTTGTCTGGTCTTGCTTACGTTTCCATGATGTCACTGTGGACTGGCCAGTGTTTCACAGTAGCTTGCTACTTCGGTCAGTCAGGTAGACATATTTTCATGTGAGATGACCCTCTTTGAAGGAACCAATTGTTACGACAGTTGAATGGTATAATCATGGGCTATTAGATTAATCAAGCTAAAGTTTACCTTTAGATCCAACAAAGTAAAAAAATGCATTTTTCTGCAAACATGTTATGTTTGGGCTTCCAGAAACACCCTGGACCGCCGCTGTCAGTATCCTATAAGCCAAGCAGCCATCCCATCAACCTGCCAACAAAGCCAGCCATCGATATTTTTAAGTGCTTGTTTGGTTTTTCCTCTCTTCAGATGATCAGGACAGCCAAGGAAACTCTAGAGGGCCTAAACTCCAAATCTTCTGTCCCAAGTCAAGTGTCTTTGTGAGAAGCAGGCCACAAGGAACAATATGTTTCATTCTAGAGTCTTTTATTAATTGATTGTCTTTCTCCAGACTTATTAATAGCTGATGATTCAGGAGCACACGGCCTGGGTCACAGTCACAGAAATCCGGGATTATTCGTACATGTAGCTTCCTCTTCGTCCTCTGACTGGTCAAACAGTGGGGAAAGGTCCCTGTGGTCCTACAGTCGGTCAGCGACACAGGACTGCTCCCCAGCTTGGTTCCTTCTTTCATCTTCTCTGGCAG
Seq C2 exon
CTTTTGAAGGACTTCCCAGACGAGCTCCGCTCCGACATCACCATGCACCTGAACAAGGAGATCTTGCAGCTGTCCCTGTTCGAGTGTGCCAGCCGGGGCTGCCTGCGGTCTCTGTCTCTGCACATCAAAACCTCCTTCTGCGCCCCTGGGGAGTACCTGCTGCGCCAGGGGGACGCTTTGCAGGCCATCTACTTCGTGTGCTCGGGCTCCATGGAGGTTCTTAAAGACAGCACGGTGCTGGCCATCCTCG
VastDB Features
Vast-tools module Information
Secondary ID
ENSBTAG00000012798:ENSBTAT00000017003:6
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:
PF0052026=Ion_trans=PD(4.7=14.9)
A:
NA
C2:
PF0002724=cNMP_binding=PU(45.5=47.6)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
AGGTGGTCCCTCTATCACAGC
R:
GAGCACACGAAGTAGATGGCC
Band lengths:
344-1203
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Pre-implantation embryo development