Special

MmuEX0025072 @ mm9

Exon Skipping

Gene
Description
potassium inwardly-rectifying channel, subfamily J, member 5 [Source:MGI Symbol;Acc:MGI:104755]
Coordinates
chr9:32122368-32151822:-
Coord C1 exon
chr9:32151689-32151822
Coord A exon
chr9:32129666-32130604
Coord C2 exon
chr9:32122368-32125487
Length
939 bp
Sequences
Splice sites
3' ss Seq
TTTAATTCACTGTATCTCAGCTA
3' ss Score
4.65
5' ss Seq
CAGGTAAGA
5' ss Score
10.77
Exon sequences
Seq C1 exon
GGGGCGTCTGCCCGTCCGTAGGCAATGCCTGAGGCTAGGGAATCCCCTGGAGAGCCCTGAGAGCCACCTGCACCGCCTTGGAAGGATCTCCAGAAGTTAGCCCCAAGGGTTCGGAGAAGCTCTCTGCGCTACAA
Seq A exon
CTATGGCCGGTGATTCTAGGAATGCTATGAATCAAGACATGGAGATAGGAGTCACTTCCCAGGACCACAAGAAGATTCCCAAACAGGCTCGGGATTACATCCCCATTGCCACAGACCGCACCCGCCTGCTGACAGAAGGCAAGAAGCCACGCCAGCGCTACATGGAGAAGACTGGCAAGTGCAATGTACACCACGGCAATGTTCAGGAAACCTACCGCTACCTAAGTGACCTCTTCACCACCCTGGTGGACCTCAAATGGCGCTTCAACCTTCTGGTCTTCACCATGGTCTACACCATCACCTGGCTGTTCTTTGGCTTCATTTGGTGGCTCATTGCTTATGTCCGAGGTGATCTGGATCACGTGGGTGACCAAGAGTGGATCCCTTGTGTTGAAAACCTTAGCGGCTTTGTATCTGCTTTCCTGTTCTCCATCGAGACAGAAACAACCATTGGGTATGGCTTCAGAGTCATTACAGAGAAGTGTCCAGAAGGGATCATACTCCTTCTGGTGCAGGCCATTCTGGGCTCGATTGTTAATGCCTTCATGGTGGGGTGCATGTTTGTAAAGATCAGCCAGCCAAAGAAGAGAGCAGAGACCCTAATGTTTTCCAACAATGCCGTCATCTCCATGCGGGATGAGAAGCTGTGCCTCATGTTCCGGGTAGGGGACCTCCGAAACTCCCACATCGTGGAGGCCTCCATCCGTGCCAAGCTTATCAAGTCCCGGCAGACCAAAGAAGGAGAATTCATCCCCTTGAACCAGACCGACATTAATGTGGGCTTTGACACTGGTGACGACCGCCTCTTCCTGGTCTCCCCACTCATCATCTCCCACGAGATCAACGAGAAGAGCCCTTTTTGGGAGATGTCTCGTGCTCAACTGGAACAGGAAGAGTTCGAAGTTGTGGTCATACTAGAAGGAATGGTAGAAGCAACAG
Seq C2 exon
GCATGACTTGCCAAGCACGGAGCTCTTACATGGATACAGAGGTGCTCTGGGGTCACCGATTCACACCAGTTCTCACCTTGGAAAAGGGCTTCTATGAGGTGGACTACAACACTTTCCATGACACCTATGAGACCAACACACCCAGTTGCTGTGCCAAGGAGCTGGCGGAGATGAAGCGGAGCGGTCGGCTCCTCCAGTACCTTCCCAGTCCTCCCTTGCTTGGGGGCTGTGCTGAGGCTGGGAACGAAGCTGAGGCCGAGAAGGATGAAGAGGGTGAGCCCAATGGACTGAGTGTGTCCCAGGCCACCAGGGGCTCAATGTGAAGTCTGTGTGCTACCCAGAGCCTCTTCTTGCCAGACACCGAGGAGCCTGGGAGGCCAGAGAGGCCAATTAGTTGAGCAAGCTTTGTGGGGCCCCAGGAGTATGGAAGCTCTACAGAGAGGAATAGTGTGTCAAGGCCTCACATCTCCTCCTTGGGGCCTCAGAGAAAGTAGCCTTGC
VastDB Features
Vast-tools module Information
Secondary ID
ENSMUSG00000032034_MULTIEX1-2/2=C1-C2
Average complexity
C1
Mappability confidence:
100%=100=100%
Protein Impact

ORF disruption upon sequence exclusion (Ref, Alt. ATG (<=10 exons))

No structure available
Features
Disorder rate (Iupred):
  C1=NA A=0.016 C2=0.271
Domain overlap (PFAM):

C1:
NA
A:
PF0100715=IRK=PU(77.3=82.7)
C2:
PF0100715=IRK=PD(22.4=69.4)


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
CCAGAAGTTAGCCCCAAGGGT
R:
GACACACTCAGTCCATTGGGC
Band lengths:
343-1282
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Pre-implantation embryo development
  • Neural differentiation time course
  • Muscular differentiation time course
  • Spermatogenesis cell types
  • Reprogramming of fibroblasts to iPSCs
  • Hematopoietic precursors and cell types