Special

MmuINT0085520 @ mm9

Intron Retention

Gene
Description
potassium voltage-gated channel, subfamily H (eag-related), member 6 [Source:MGI Symbol;Acc:MGI:2684139]
Coordinates
chr11:105875699-105878974:+
Coord C1 exon
chr11:105875699-105875904
Coord A exon
chr11:105875905-105878548
Coord C2 exon
chr11:105878549-105878974
Length
2644 bp
Sequences
Splice sites
5' ss Seq
CAGGTATGG
5' ss Score
9.99
3' ss Seq
ACCCATGGCTTCCATCCCAGGTC
3' ss Score
7.38
Exon sequences
Seq C1 exon
AGGGCTCTCACAGCAGGCCAAGCGGACAGGGGCCTGGTCCAGGCAGGGGCAAGTATGGAACTGTCAGCCAGATCCCGCAGTTCACGCTCAGCTTTGTGGAGTTCAACCTGGAGAAGCACCGCTCAGGCTCCACCACAGAGATTGAGATCATCGCTCCCCACAAGGTGGTGGAGCGGACACAGAATGTCACTGAAAAGGTCACGCAG
Seq A exon
GTATGGGTCTGCAGGAGAGCGGTGAGGGTGGGCGGGGTCAGAACCCCTGGGTCCCTTGGACCTCAGCTCTTTTAAGGTCATAACTAAGAAGGGAGATGTGACTTGTCCAACCTCTCCCTGCCCCCCACCTCACATCTTGGTCTGAGTCCCCAGCCTCGTCTTCTATAGTTTGAGTCAGATTCTTAAGACCTGAAGGCCTGGTCTGAGGCCACAGCCCTGAGGCCTGAAATCAGCAGAGGTTGGGGTGAGCAAGGCCTATGAGTACTTCCGAGGCCTGGAGATCCCAGAAGGATAGGAGGAGAAAACACACAGGCCACCTTGGGGCCAGCCTATGGTTCTGCAGTCACAAGGCAGGAGTGGTACAGAGGGTCAAGCCCATGCAAAGATGAGGAGAGGAAGGAGGGATGGGATGAGCCCTGCCCTGGTCCTGCTCCTTCCCTCTGCTTTTGGGACGATGGCCACTCCTTGCGTTGTATGCAAACAGTACACCTGGCAGGAGTGGGGTAGTGTCGGTGTCTCTAGCTAACTTTGGATCCTGGGGATCCATCTCTAAATGCCCCTCCTGTGCATCTTCTATTTGGCACATGTCCCTTACTGGGTCCTGGGTTTCATCTGACCCCGACAGTCCCTTCTAAGGGGCTTGTTGGCCTGATTCTTCCAGGGGCAATTGACTAGAACCCTGCTTGAGACTGGAGTCAATAGGATGCTGGCACTGGCACACTATGTGACCTTGACAAAGGACACCCCTACCTTTGGGCCTCAGAGCTCTCATATGCAGGAAAGAGTTAGGCCAAATGATCTCTGAGGACCCATTGACATTAAGTAGTGCCAGCTCAGGTGACAGAAGGGGACTTTGTTAAGCCGTAGAGAAGAGCCTAGGATACGGATGAGCAAGGGACTGCAGAGGGGACCATACAATCCATTTCCTGACCCTTCTCATCTGAAGCATAGCCAATGCCAGCACCAGCTATGGAGGAGACCATTTAGCCTCACAGACAGGACTAAGAAGAGGCCTGGCAGGGAGAAGAGCTCTGGTATCCAGGGGTGTGGCACCATGACCTCCTACTTTGCATCTGAGTTCAGCTACCAGGGATACTTTGGTGAGCCTTGGTTGAAAGCCCACATGGACCCAGATCTGGCTGGGTGAGGGGACATAGGTTACTGAGGTGACTATGGAGACAGGGCTACATATAGGGGTAGAGAAAAAAAGATCCCTGAAAATAAGAGGGTCCAAGTCAATGTAGGACCCCAAGTGGGTCCCTGAGGATGTAAAAGATGGGTGGAGGCTGGAAGCCGAGCAGGCAGAACACGGTGGCTCCCACTTAGGTGTCTGGTTGTCAAATCAGTACCATTTTAGGGAGAATCAGTCCTTAGATTGATTTCTTTTGTCCTATGATCCCATCTCTTGACTCTACAAGACCAGAGCCTAGAATGGCTGGTCTCCTTATAACAGCAGCGATGATGGAAGAGTCTGTGGGGATGGTCAACCCCACCACCATCCCATCCTTACTGAGACCGTGTCGGTCAGATGGTGGAGAAAGGATGAGCTAGGACAGCGGTTCTCAACCTATGGGTTGCGACCCTTGGGGGGGGGGGCGTGTCACACATCAGATATCCTGCATGTCAAATATTCACCTTATGACTTATAACAGTCACAACATTACAGTTATGAAGTACTGACAAAAGGATTTTACAGTCGGGGGTCACCACAACACAGGGAGCTGTATTAAAGAGGTGCAGCATTAGGAAGGTTGCAGACCACTGCCCTAGAAGCAGGCAGATACATCTTGTTTAACTACATTCCTATGCAGTCTGTTGTCCGTTTTACCCATGAGGGAACAGGGGATCACAGGTTACTAGGCTTGCTTCAAGGCACCAAAGAAACAAATGGCAGCCCTGGATATTTAGCCTGGAGTCTGGCTTCAAAAACACCTGCCCTTCCTGATTCCCCCAGCTGCTTTGCTTCGTGTTAGGCAGCTGGGAGTTGTCGGTTTCTGTCTTAGCAACCATCCATTGCTATAGTCTTGGAGGCACCGAGATGAGAAGAGGATGCTTCACAGATGGCAGTGACTCATGTGTGATGGAGATTTGGCTCTTTCCATGGGATGCTCTGAGAGTCGCCCCAGGGAGGAACCTCATTGGCCCTTAGGAATAAAGACTCTTCTGGAAGTGACTTGTTCCCATCAAGAATCCCAAACTTGGGTAGGGGCGTTAGCTCAATGGTAGAGAACTTGTCTGCCCTGTGTAATAAGGCCCTAGTTTTAATCCTTAGCACTAAAACTAGAACAAGCAAACAAGCAAGCAAGCAAACACCAATGGCCACCCAAAGCCTATTATAGACAACCAGCCCAGCAAGCTATCTCAACCCAGGTTTCCTTAAAACATACTCACCAGGCCTGGCCCTGCTCACCCCAAGAAGAGCTGTTTCTGGGAAAGTTTGTGAGCTACCAGAGATCAACCATGTGGCAGAGCCCCCTGCTCTCTCCCTCTGTCCTACCTCCTCCTGACATACCTGTCCCTCATGTGCCCTTCCTTTGTCCTTCTGCCTTTCATGACTGTGACAGTTCTCCTCCCTAGTCCTCCCCATAGACCGGTCTTCCTAGCAGTGGCTGTCCCCACTGACCACCCATGGCTTCCATCCCAG
Seq C2 exon
GTCCTGTCCCTGGGTGCAGATGTGCTGCCAGAGTACAAGCTGCAGGCACCGCGCATTCACCGAGGTACCATTCTGCACTACAGCCCCTTCAAGGCTGTATGGGACTGGCTCATCTTGCTCTTAGTCATCTATACAGCGGTCTTCACGCCCTACTCTGCTGCCTTTCTGCTTAGCGACCAGGACGACTCACAGCGTGGTACCTGCGGCTATACCTGCAGCCCGCTCACCGTGGTGGACCTCATCGTGGATATCATGTTTGTGGTGGATATTGTCATCAACTTCCGAACCACCTACGTCAACACTAATGACGAGGTGGTCAGCCACCCCCGACGAATCGCCGTCCACTATTTCAAGGGCTGGTTCCTCATTGACATGGTGGCTGCCATCCCTTTTGACTTGCTTATCTTCCGCACTGGCTCAGATGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSMUSG00000001901-Kcnh6:NM_001037712:4
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.237 A=NA C2=0.000
Domain overlap (PFAM):

C1:
NO
A:
NA
C2:
PF0052026=Ion_trans=PU(31.0=45.8)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
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
  • Muscular differentiation time course
  • Spermatogenesis cell types
  • Reprogramming of fibroblasts to iPSCs
  • Hematopoietic precursors and cell types