Special

BtaINT0079588 @ bosTau6

Intron Retention

Gene
Description
potassium channel, voltage gated eag related subfamily H, member 4 [Source:HGNC Symbol;Acc:HGNC:6253]
Coordinates
chr19:42930473-42934086:-
Coord C1 exon
chr19:42933929-42934086
Coord A exon
chr19:42930681-42933928
Coord C2 exon
chr19:42930473-42930680
Length
3248 bp
Sequences
Splice sites
5' ss Seq
GTGGTGAGT
5' ss Score
8.95
3' ss Seq
CTGCTGCGCCCACTCTGCAGACA
3' ss Score
7.53
Exon sequences
Seq C1 exon
ATATCATCCTGAACTTCCGCACCACCTATGTGTCCCAGTCTGGCCAGGTGGTCTCTGCTCCGCGTTCCATTGGCCTCCACTATCTGGCCACCTGGTTCTTTGTTGACCTTATTGCTGCTCTACCTTTTGACCTGCTTTACGTCTTCAACATCACCGTG
Seq A exon
GTGAGTGAACCCTGTCCTGCCTTGCAGCCTAGCCTGGCAACTTCAACACAGCATCTCCCATTAAGGGACCCACCTCAGTCCCAGACTCAGTCATCAGCGAATATTTGCCAGGCATCTGTGATGGGCAGAGCCCAGCACTAGAAACCAAGAAGGATCCAAGAGCATCTGCCTTCTTGGGGAGTTCAGCTCACAGTCTCTGAGGGAAGCTGAGACAAATGAAAATCTAACTAGGGCTACCAAGGCGGCATTGGTCTGCAGCCAAATGAGTGGCACTTTTCACATTTTTATTTAACAAACAACGGATGAGCATTTAGCTGTCTGCAAAGCACTGTGTAAGGCATGGTCACTGTGGAGGAGAGGGATAAGGATTCAGCTACTCGGCAGCTAAGCTGGTGGAGACAGCAGAAGCAGAAGAGGTGAATGGACTGCAAGACAGGGCCCAGGTAGTGCTGCACAGGGGCTGGACGCAGAACTAACCAACCTTGGGATTCCAGGCTGGAACACAGGCTCCCACAAAACTGATCTGAAATCTGGCTGTTGCGAGGAAGCCAAAGCATGGCAGTTGGGCAGAGGCTGGCGTGGTCTAGGAAGGGTTCCCGAGGGAGGAGGTGAGAGCTGAGCTAGACCCTAGACAGAATAGGCCCCAGCTGGCAGGAGACAGGAGAGGGAACATTTAGGGGGAACGTAGCAAGCCAAGATGAGGAGGTAGAGGCTGCGGGGCGGACTTGGAGGCAGAGAGTCCTAGAACTGCCTGGAGGCGCCCTCAGTGGTCAGCTCTGCACCCAGCCGGCAGATACTAGGTCTTCTATGGCCCAGGGAGAGGGAGTCCCACCCTGTGTCCCCAGACCCCCTTGAGTGGGGAGGTGGAGAGCAGTCTCCCCGTGTGCTCCTCTGCCTGCCACACTCAGCTATAGCGGGAAACCACCTACACGCAGCCGGATTTAACTAGCCGCCAACGGGCTGTGGGCCTCTTCTCCTGGCTGTGTACACGTGTGTGCATGCTCCCACACACGTGCATGTGGGTGTGTCTGCCCTGAGGCTCTGGCCCTTCCAAGTGGAGCTCCCCACTTCTCCCCTGGGTGCATCCCCACCTGGTTTGTGCCCACCAGGCAGTCCCCCCTTCTCCGGTAGCGTCAGGAGTACTTTACAGTTTTCTAAGTTCTTTCACACATCATCACGTAGGAGCCTCACAGTAACCTTTCAGGGAAGATTCTCATATCTCTCTTTCTCAGAGGTAGATGCAGAGGCTCAGAGAGGTTGAGTGGCTTGTTGAAAGTCACACAGCTAGCAATGGCAGACAAGAGACTAGAATCAGGTCCCTAGACTCCCGGTCTAGAATTCTTTCCAGCATGCCACCCTGCTTCCCAGGAAACCAGTGTACCTGAGTGGATGGCCTGGCACAAGGAGGAAGGAGGAGCCATGCTGGGGCTAGAGGGAAGCAGAGCAAAGATGGAGGCTAAGTAGGCACTGGCAGAGCCATGGACTTGAAGGAACCAGGCCTGAGACATCCTGGTCCAACGAGGAAAGGAGGGCCCCAAGGGAGTAGGGCCCAGGGGTAGGTGACAAGGGGAAGCCTTGAAGAACTCAAGGTTGGAGTCAGGAGCTCTGAGAGCTAGGGGCAGGCATTAAACCCTGAAGTGCGTGTTCAGTAGCTAAGTTGTGTCTGTCTCTTTGAGACCCCATGGACTGTAGCCTGCCAGGTTCCTCTGTCCATGGAATTCTCCAGGCAAGAATACTGGAATGGTTTCCCCTTTCCTTCTCCAGGGGATCTTCCTGACCCAGAGATTGAGCCTGAGTCTCTTGCATTGGTCGGCAGATACTTTACCACTGAGCTCCCTGGGAAGCTCCTAAACTCTGGAGAGGGTCCATCAGAGTCACCTCCTTTCCAACTCCTTTGTCTAAAATTAGAGAAAATGGCATGCGACTCAGGAGCTGTGTAGGGCCAGGGGGGATGCTCCTGGAAGCCCCTGAAGGGACAGTGAGGGGCCTTCATACGAAGTTCCACATGTGCTTCCCCAGAGCCCCCGCCCTAGCCTCCAGGCTGCCCCAGCCACAGCAGTGAGGACATAAGCTCCCACCTGCGTATCATGTCCAAGACTGGAAGGGCTTATCAAAACACAACCAAAACAGTCACAGTTAATACCAGCTAACCCTTACAGGACCCTGACTAACTTCAGCAACTCCCACCAAACCCTGCAAGGGCTGGGGCCTCACAGTCTAAGTACCCTGCTCTCCTTCTCTCAGCATCCCAGCTGTAGCTGATCCATAAGGGATGAGGTCCCTAAACCTTCCCCTGTCCACAGCTGATTGTACTTAAGACACTGGGGGCTTTGAGCAAGGACCAGAGATCATTATGTCTGTTGTCCTGCCTCTGCTGCTGCTGCTGCTGCTGCTGCTGCTAAGTCGCTTCAGTCGTGTCTGACTCTGTGCGACCCCAGAGATGGCAGCCCACCAGGCTCCCCCGTCCCTGGGATTCTCCAGGCAAGAACACTGGAGTGGGTCGCCATTTCCTTCTCCAATACATGAAAGTGAAAAGTGAAAGTGAAGTCGCTCAGTCGTGTCTGACTCTTCACAACCCCGTGGACTGCAGCCTTCCAGGCTCCTCCGTCCCTGGGATTTTCCAGGCAAGAGTACTGACGTGGGGTGCCATTGCCTTCTCCATGTCCTGCCTCTGACTTGCCCTTTTACCAGCCAAGGTGCTAAGAGGCAGTATAGCACAAAATGGACTCTGGTGTCAACTCAGATTTGAATCCCAGCTCCATGATTTCCTTGGTCTGTGCCCTTGAGCAAGTCACCAGCCTCTCTGAACCCTAGTATACTCATCTGCACACTGAGAATGGTGACGAAAATTGGACTGAAGGTGTACGTTTGTCTGTTTTTACGAGGATTACAGTTATTTAGCCCAGTGCCTGACCCACATAGTACTTGCTGTTAGCCATTATTAGGGTTGTGTTGTTGTTGTTGTATTGGTCGCCGCACTGCATGGCTTGTTGAATCTTAGTTCCCTGACCAGGAATTGACCTCTTGCCCCCTGCAGTAGAAGTGCAGAGTCCTAACCACTGGGCTGCTAGGGAAGTCCCCATGATTAGTTTTAGTATCATCCTGTCCCCCTTGCATTTCCTGGTCACCTTCTCAGCACAGCAAGGATCCTTTCCCTCAGGCAGCTTCCCCTAGCTCCAGGGCACCTGGGGGAGGGGGGAACGTTGCGGGGCCTGCTGACAGCCTCCCCTGCTGCGCCCACTCTGCAG
Seq C2 exon
ACATCGCTGGTGCACCTGCTGAAGACCGTGAGGCTGCTGCGGCTGCTGCGGTTGCTGCAGAAGCTGGAGCGGTACTCGCAGTGCAGTGCCGTGGTGCTCACGCTGCTCATGTCGGTCTTTGCGCTCCTTGCCCACTGGATGGCCTGCGTCTGGTATGTCATCGGGCGCCGGGAGATGGAGGCCAACGACCCCCTGCTCTGGGACATCG
VastDB Features
Vast-tools module Information
Secondary ID
ENSBTAG00000001195:ENSBTAT00000005335:6
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=FE(24.8=100)
A:
NA
C2:
PF0052026=Ion_trans=FE(32.9=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:
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