Special

MmuINT0085464 @ mm9

Intron Retention

Gene
Description
potassium voltage-gated channel, subfamily H (eag-related), member 2 [Source:MGI Symbol;Acc:MGI:1341722]
Coordinates
chr5:23827063-23827640:-
Coord C1 exon
chr5:23827454-23827640
Coord A exon
chr5:23827241-23827453
Coord C2 exon
chr5:23827063-23827240
Length
213 bp
Sequences
Splice sites
5' ss Seq
CAGGTAAAG
5' ss Score
9.65
3' ss Seq
ATCTTCCTTCCTTGCCCCAGGCT
3' ss Score
8.72
Exon sequences
Seq C1 exon
GTGCCTTCTCTGGGGTGTCCAATATTTTCAGCTTCTGGGGGGACAGTCGGGGGCGCCAGTACCAGGAGTTGCCTCGATGCCCTGCCCCTGCCCCCAGCCTCCTCAACATCCCCTTGTCTAGCCCTGGTCGGCGATCCCGGGGTGATGTGGAGAGCAGGCTGGACGCACTCCAGAGACAGCTGAACAG
Seq A exon
GTAAAGATGGGTGCCCAGGGAATGGGCACGGGGTAGGCTGCACTGTGGGGGAACTTGGGGCCTCTTTGGGTTTCTGCTGATGTTTCAGGGGTGCTCTGTCTAGGACTGTCTGTGCCAGGCAGGTGGACCCTCTCCTTCCTCAGCTGCATGAGGAGGGAGCCTAGAGTGAACCAGCTATCTCCACTTCTGAGAAATCTTCCTTCCTTGCCCCAG
Seq C2 exon
GCTGGAAACCCGGCTAAGTGCAGACATGGCCACTGTCCTACAGCTGCTACAGAGGCAAATGACCCTGGTCCCTCCTGCCTACAGTGCTGTGACCACCCCTGGGCCCGGCCCCACTTCCGCATCCCCTTTGTTGCCTGTCGGCCCTGTCCCCACTCTCACCCTGGACTCGCTTTCTCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSMUSG00000038319-Kcnh2:NM_013569:13
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.714 A=NA C2=0.583
Domain overlap (PFAM):

C1:
NO
A:
NA
C2:
NO


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:
AGTACCAGGAGTTGCCTCGAT
R:
GAAAGCGAGTCCAGGGTGAGA
Band lengths:
304-517
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