Special

MmuINT0007547 @ mm9

Intron Retention

Gene
Description
ATP-binding cassette, sub-family A (ABC1), member 1 [Source:MGI Symbol;Acc:MGI:99607]
Coordinates
chr4:53049745-53051163:-
Coord C1 exon
chr4:53051029-53051163
Coord A exon
chr4:53049849-53051028
Coord C2 exon
chr4:53049745-53049848
Length
1180 bp
Sequences
Splice sites
5' ss Seq
CTGGTGAGT
5' ss Score
10.1
3' ss Seq
TTGTTTTATTCTAATTATAGGAT
3' ss Score
8.18
Exon sequences
Seq C1 exon
GTTGGTGAATGGGCAATTCGCAAACTGGGCCTGGTAAAGTATGGAGAAAAATATGCCAGTAACTACAGTGGCGGCAACAAACGAAAGCTCTCCACAGCCATGGCTTTGATTGGCGGACCTCCTGTGGTGTTTCTG
Seq A exon
GTGAGTGTGAGAGGGGTGTGAGTGAGTGGAGGGTGGAAATTGTTCTTCTGTCTTGAATAGACATCATGGCTTATCTGAAGTCACATGTAGGCCTTTGCGTACTTGGCATGGTGATAGCAAGTCCATCTGCTGGTCCAGAGCAGGCTTCTCCCTCACAGTTTCTCCCTCACAGCTTCTCCCTCACAGCTTCTCCCTCACAGCTTCTCCCTCACAGCTTCTCCCTCACAGCTTCTCCCTCACAGCTTCTCCCTCACAGCTTCTCCCTCACAGCTTCTCCCTCACAGGCTTCTCCCTCACAGCACGCTGGGTGGCTCGGCTGTACCTTTACAGGCTCCTGAGTAGACAAGCTCCACTCATCTTGTTTCCTTGCCTTAGATAATCCCTACAAACATGGCTGAAGGTGAAGGTGCTATTTGAATAGTCTCAGGAATATTCTTCATGACTCTATGTTGTTCATCCTCCAAAGGTAGAAGTGAGGACATGGCTTCTAGATGGACATAGTAGCCACAGATGACCATAGTAGCCACTGCATCATAGTTGCTCCCATACAGATGAATAAAAACCAGACCAGACTGGGCAGTGGTCCTTGATCCTCATTTTGTAGAGAACACTGGGAGTATGGGAAGAAGCCTTGGGTTGAAGCTTTAATTTTTATTGACCATGTGGATATGAAATTTCTCTATGATTAGCAAATGTAATAGAACAAGGAGAAAAATATGATGTAAGTTTCACTGCTCTGACTTCAAAAATAATTTTGGACAAAAAGTTTTGGGGTTTTTGTTTTGCTGTTGTTGTTGTTTTGCTATAAGGTTTCACTATGTAGCCCTGGGTGGCCTAAAACTTCCTATGTGGACTAGGCTGACTTTGAGCTCATAGAAATCCACATGTCTCACCCCACCCCCACTCTGGGAAACCCGGCATGATCATTAGCATTGAAAAAAAATTGTCTTGGGCTGGAGAGATGGCTCAGTGGTTAAGAGCACTGACTGCTCTTCTGGAGACCCTGAGTTCAATTCCCAGAAATCACATGGTGGCTCACAACCTTCTGTATTCTGTAATGGGGTCTGATGCCCTCTTCTACAGTGTACTCACATATATAAAATAGATAAATAAATCCTTTTAAAAAATTGTCCTTGACATTTTTTTTCCAGCAAATAAACTTGTTTTATTCTAATTATAG
Seq C2 exon
GATGAACCAACCACAGGCATGGACCCTAAAGCCCGGAGATTCTTGTGGAATTGTGCCCTAAGCATTGTCAAGGAGGGGAGATCTGTAGTCCTTACATCTCATAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSMUSG00000015243-Abca1:NM_013454:46
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.000 A=NA C2=0.029
Domain overlap (PFAM):

C1:
PF0000522=ABC_tran=PD(17.2=54.3)
A:
NA
C2:
PF0000522=ABC_tran=PD(2.8=11.4)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
Conservation
Human
(hg38)
No conservation detected
Rat
(rn6)
No conservation detected
Zebrafish
(danRer10)
ALTERNATIVE
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
GTTGGTGAATGGGCAATTCG
R:
TATGAGATGTAAGGACTACAGATCTC
Band lengths:
238-1418
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