Special

MmuINT0145564 @ mm9

Intron Retention

Gene
ENSMUSG00000046329 | Slc25a23
Description
solute carrier family 25 (mitochondrial carrier; phosphate carrier), member 23 [Source:MGI Symbol;Acc:MGI:1914222]
Coordinates
chr17:57196005-57197657:-
Coord C1 exon
chr17:57197531-57197657
Coord A exon
chr17:57196093-57197530
Coord C2 exon
chr17:57196005-57196092
Length
1438 bp
Sequences
Splice sites
5' ss Seq
ATGGTGAGA
5' ss Score
7.23
3' ss Seq
CTGGGGCTCCCCTTTTCCAGGTC
3' ss Score
10.5
Exon sequences
Seq C1 exon
GGTGTCTCCTCTGACTGGGATGCTGATCCTGATGGTGGCCTCAGCCTGGAGGAGTTTACTCGCTACCTGCAGGAACGGGAGCAGCGCCTTCTGCTCATGTTTCACAGCCTTGACCGGAACCAAGATG
Seq A exon
GTGAGATGGGCTCTAGGCTGGGGAATGGACAAGTGGGTTAGAACCCGAAGCGCCGGGGGAATGGGGAGGGCTGCTTCTGACTCATGGACTATTTTGGGAGTTCTCAGCTGCAACTAGGTGATTTGAGCCTGAACTGGCCCATCCCACCTCCTATCCCTTTTGCAGTAGGACCCCTCTCTCTGCCCATACACGTTTCTCTTCAGACAGTATACTTGGTTCGGAGACCCTCAAATACAAGGATAGACCCTTAACCAAGCATCTTCTGGGTTCCTTAAGTATTACCTTAAAGTTGGAGAGCTAGATCAGGGGTAACGTGGTTGCCACAAAGCCACAAGTCCCTAAGCTCAATCCCTTGTCCCCATAGATGCAGAGGTACATGCCTGTAAGCCCAGCCTTGGAGAGGGGGAGATGAAGAAAATGAATAATAATCAAATATTGCTTTAGTCCCTTGTAACATAGGAACCTCTGTGATCACCCCTGAACTCACGCATTCACTCCTGGAATAGAGAACTCTCCAATATCAACCCTGAGCAGCCCCCACAACCTGTATAAGAACCTCTCTCCTTACCATGGTGGCAAACAACTTTGATCCCAGCACTCAGGAGGCGGAGGGGCAGGCAGATGTCTGAGTTCAAGGCCAGCCTGGTCTACAGAGTGAGTTTCAGGACAGCCAGGGCTACACTGAGAAACCCTGGCTCAAAGGAGAGGTGGGAGGAGTCTCCCATGAGGCTGAGAAGCTGACTCAGTCAGAGAGGGACTGGAGTTCAAACCCCCGCACCTGTGTTAAAAAGCTAGGTATGGGGCTGGTGAGATGGCTCAGTGGATAAGAACACCGACTGCTCTTCCAAAGGTCCTGAGTTCAAATCTCAGCAACCACATGGTGGCTCACAACCACCCGTAATGAGATCTGACGCCCTCTTCTGGTGTCTGAAGACAGCTACAGTGTACTTATGTATAACAATAAACATCTAAAAAAAAAAAACCACTTAAAAAAATAAAAAAGCTAGATGGGCATGGTGGTGCACGCCTTTAATCCCAGCACTGGGGAGGCAGAGGCAGGCGGATTTCTGAGTTCAAGGCCAGCCTGGTCTACAGAGTGAGCTCCAGGACAGCCAGGGCTATACAGAGAAACCCTGTCTCAAAAAACCAAAAAAAAAAAAAGCTAGGTATGGTGGTGCCCACCTGTGACCCAGCACCGGTGAGGTAGAGACTGGAGGTGGTAAGGTGGATCTTAGGGTTAGACTTCCAGATAAGTCACCGGACTCCAGGTTCAGCAAGAGACCCTGTCTCAAAAGAAAGATGGAGAAAGACTGAAGACAGCCATTGACCTCTGGCCTCTTCATCCACACGCACACAGAAGCACACACACAAGGGCTTCTGGACCTCCCAGTCCAGCCTATGTATGGTTTGGGTGTCTCCTGGGGCTCCCCTTTTCCAG
Seq C2 exon
GTCACATAGATGTCTCTGAGATTCAACAGAGCTTCCGAGCACTAGGTATCTCCATCTCACTGGAGCAAGCAGAGAAAATCCTACACAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSMUSG00000046329-Slc25a23:NM_025877:2
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.256 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF134991=EF-hand_7=PD(33.8=51.2),PF134991=EF-hand_7=PU(28.4=44.2)
A:
NA
C2:
PF134991=EF-hand_7=FE(43.3=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GGTGTCTCCTCTGACTGGGAT
R:
TGTGTAGGATTTTCTCTGCTTGCT
Band lengths:
214-1652
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