Special

MmuINT0010414 @ mm9

Intron Retention

Gene
Description
actinin, alpha 1 [Source:MGI Symbol;Acc:MGI:2137706]
Coordinates
chr12:81272716-81274129:-
Coord C1 exon
chr12:81273950-81274129
Coord A exon
chr12:81272863-81273949
Coord C2 exon
chr12:81272716-81272862
Length
1087 bp
Sequences
Splice sites
5' ss Seq
GAGGTAAAT
5' ss Score
8.39
3' ss Seq
GGCTTGATTCTTGCTTCTAGCAT
3' ss Score
6.09
Exon sequences
Seq C1 exon
GAGATTGGGAGGATTTCCATTGAGATGCACGGCACCCTGGAGGACCAACTCAGCCACCTGCGGCAGTATGAGAAGAGCATCGTCAATTACAAGCCAAAGATTGACCAGCTGGAGTGCGACCACCAGCTCATCCAGGAGGCACTTATCTTTGACAATAAGCACACCAACTACAACATGGAG
Seq A exon
GTAAATAGGCCTGGCCTCTTCCTAGCCTCCATTTGGGGTAGCATCTCCCAATGAATCAGGCTGGAGGAGGAGAAGGAGGGTTATGCTCTCTGCCCCTGAAACTCTGCACCTTCAATCTGCTGTACCTTCTGGATGCCAGACAACTTGTTGCAAGTATGCACATCTGGTCCCTAGCTGGAACTGAATGAGCCTTGGTTTGTAACAAGCACTCCCCAGTGATTATGATGCTATGGGCTCAAGACATCACTGGCTTAGGTACTTCCTAAATGATGTGAGCTCTTCATCCCTTAATAACAGGATATGTTCTGAGGTTTGCCTCGTTAAGTGGTCTCCTCTTTGTTCAAATATCAGAGTGTGCTTTCATTGGCTGCAGTGTTACCATGCAGCCACTTGAGACCACCGTGGTGTATTTGACTTGTCACTGATCAGAAGGCCATTATGTGGTGCCAGCTGTGTGGGTTTCCCTCAAAGGTTTATTTGTGGATGTATATGTCTGTATGTGTGGCTGCGGGGTAGGTCTTGCTGGGATGGGGGCATTCTGGTTTTTTAGCTTTTCCCACCACAAAATCTACCTTCCTTCACTAGCAGAGTTCCAATGGTAAATCCGGATCTTGTAGCTTTTTTTTTTTTTTTTTTTTTCAGGCAAAGGCCTGTTCTTTCTGGCCTCTTTCAGGCCTCCCATCCTGATAGGGTGTGATGTGTCCCTCCTGATGGTGATACTGTAACTATAGATAGAAGATCAAGTTAAATGTTTTTTTTGGTTTTTTTTTTTTTTTTGGTCTTTATCTTATGGCTATGAGTACTTTGCCTGAGTGAATGTCTGTGCACCGTGTCTGTTCCTGGTGCCGGAGAAGGCCAGAAGAGGATATATCCCCTGGAACTAGAAGTATAGATGGTTGTGAGCTGCCATAGGGGTCCTACAATTGAGCCTGGGTCCTCTGGAAAAGCAAGAAATGCTCTTAACCACTGAGACATCTCTCTAGCCCCTACTTCTGCCATGTTTGAGTTGGGAGGAGGGATAGTTAGTTGGACAGCCTGGAGCCCAGACCTGGCGCTCCTTTCTGATGGGCTTGATTCTTGCTTCTAG
Seq C2 exon
CATATCCGTGTGGGCTGGGAGCAGCTGCTCACCACCATTGCCAGGACCATCAATGAAGTGGAGAACCAGATCTTGACCCGGGATGCCAAAGGCATCAGCCAGGAACAGATGAACGAATTCCGCGCCTCTTTCAACCACTTTGACCGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSMUSG00000015143-Actn1:NM_134156:17
Average complexity
IR-C
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (disopred):
  C1=0.283 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF0043516=Spectrin=FE(56.7=100)
A:
NA
C2:
PF0043516=Spectrin=PD(20.2=42.9),PF134991=EF-hand_7=PU(31.3=53.1)


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:
ATTTCCATTGAGATGCACGGCA
R:
CAAAGTGGTTGAAAGAGGCGC
Band lengths:
310-1397
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