Special

RnoINT0136914 @ rn6

Intron Retention

Gene
ENSRNOG00000047781 | Slc25a23
Description
solute carrier family 25 member 23 [Source:RGD Symbol;Acc:1588586]
Coordinates
chr9:9991732-9994170:+
Coord C1 exon
chr9:9991732-9991843
Coord A exon
chr9:9991844-9994011
Coord C2 exon
chr9:9994012-9994170
Length
2168 bp
Sequences
Splice sites
5' ss Seq
ACAGTAAGT
5' ss Score
9.49
3' ss Seq
TGTGCAGCCCCCATCCTCAGGTC
3' ss Score
6.64
Exon sequences
Seq C1 exon
CATGGACCGTGATGGCACCATGACCATTGATTGGCAGGAATGGCGAGACCACTTTCTGCTGCACTCTCTGGAGAATGTGGAGGATGTCCTTTATTTCTGGAAGCATTCAACA
Seq A exon
GTAAGTTGGAGGCCACCTACAGGGCGGGGGCTAGCTCCAGGGTCTCCCCAGGACTCGGAAGTTCTGGGCCGAGACTCCAGAGTTGTTGTCGGTATCTGAGGCTCTCAGCTCTGAGCCTTTATTGCTCCAACTGGGGCTGGGAGCCTGATGACCACTGGTGGACAGTTCTGCTTAGAACCCTCTGGTCCTTCTTAGACTCCAGGGACAGCTAGTGGGAAGTGGGGTTACGGGGAAGAAAATATACCAAATGGTGTTCCCACACTTAGCCCACACAACTGCCAGCTGCCAGGTGCTTGTCACCTACTCCAAGGCTCCTGGGGCTGATGGAAGGATGCAGGCAGACACTGTGTCTAGAAGGTTCAAAGGAGTCCACAGGAAAGGAAAGGGAGGCCAGTTCCTGCACAGAGGTGGGAATCACTTAGGATCTTGTGGTGTCTGGAAGATTACTCTGTGGGACCTGACAGGGTTCCCGTTATGCTGGCTTTTTCTGGGGAGATGTCAATAGCATCTACTTACTCCAGCTTACGTAACAACAGACCAAAGTGAGGCTCTCACAAAGGTCCCACTTGGTGGGCCCATGAGTTTCTTCAGCGTAATTGCGGAGCACCGTGAGGGGTCACTTACAGGACCTGGGATACCCCAAACAGCTACAGCACTGCTGAGTCCCACCCCATTCATGGATGGTGACCTGGTAGAATCTGTACCATGGAGTCTTTCAATTGACCTTCTGCTTCCTTGTTAGTGTTTCCCAGGATTCCTTGCAGCTGGGGTGGGACAGTGAGCGGACTTCCAGGTTACATCCTGTGCCCCAACCCCTTTAGGGGGTGTCAAGAGCTCCATTACCATAGACCCAGTTATCACCAGATTGTTCTGCTCAGTTTGTTGCCATGGCTACCAGGCCAAGGTAATCACTGCCTAAAAATGGCACCGGGGGTGATGATGTCATGCTCAGAGAAAAAAAGCTATACTATAATCCTCTCGGGAGATCCAGAGACGTCCACTCCCCAAAAATGCACCATTGGGAAATCTATTGCTGGGCCTAGGACAGAGTACATCCCTCGGGGAGGACTCTGAGGAGAAGACTTACAGAGGAAGACACTCTAGGAAAGACACCTGGGGGAAGACTCTTGGGGAAGGATTTCTAAGGGAGGGCTCTCCATGGAGGAGATGACTGTGAAAGCAGATTCTTTTGAAGGATTCAGTGGCTCTTTTGGTGGAATCAGTGGATCTTATGGTGAGATCTGGTAGATTCTTCAGTAGGATTCAGTAGATTCTTTGGTAGGACTCAGTGGATCTTTTGGTAAGAATTGGTGACTCTTTGGTGAGATCAGGTGATTCGCTGGTGAAATCCAGTAGCCCATTTCTTAAGTTTCAGTGGATTCTTTCTTTAGGGGTGGTGTTGAGACAGGGTCTCTCTGTGTAACCATGGGTGTCCTGGAACTCACTCTGTAGTCCAGGCTGGCCTCAAACTCACAGAGATCCGCCTGCCTCTGCCTCCCAGTGCTAGAACTAAAGATGTGCGCCACCACCGCCCAGCTCAGTGGATTCTTAGTTTGTGCAGAGAGGCACAGGTAGAGGTCAAAGGACAACTTGGGGAAACATCTCTCTTTGCATCTTATGCATTATGGATGTTGAACTCAGACCTCCAGGCTTAGTTGAACACATCTATGGAGCCCTCACAAGGCCCTCAGTGTACTCCTGTGGGAGTCTATGGTTCCTTTGGTGGAATTCAGTGGACTGAATTATTTGGAGAACTCAATGGATCCTTTAGAGTAACAGTTCTCAACCTGTGAGTTGTGGCCTCTTTGGAGTTCGAAGGACCCACTCATAGAGATTGCATATCAGGTGTTTATATTACAATTCATAACAGTAACAGAAAATAATTTTATGATAGGATCAGTACAACATGAGGAACTGTATTAAATGGTCAAGCATTGGGAAGGTTGAGGACGACTGCTTTAGTAGATCCTGCAGAGGAATCCTGGCATCTCACTGACAGTTTTAGTGGCACGTGGTAGGATCCAGAAGGGATCTGCTGGGCTCTTGAAGCAACATCCTTTGGCGGGCTCTGGGATGTTCTAGAATTCATAGAGGAGACTTCTCCACTTAGGACCCAGGTACATCCCCCACCTCTGCTGGAGCCTGACATGTGCAGCCCCCATCCTCAG
Seq C2 exon
GTCCTGGACATTGGTGAATGCCTAACGGTGCCTGATGAGTTCTCCAAGCAAGAGAAACTTACAGGCATGTGGTGGAAGCAACTGGTGGCCGGTGCAGTGGCTGGCGCTGTGTCACGGACAGGCACAGCTCCTCTGGACCGACTCAAGGTATTCATGCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000047781:ENSRNOT00000073000:4
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

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

C1:
PF134991=EF-hand_7=PD(40.0=84.2)
A:
NA
C2:
PF0015322=Mito_carr=PU(34.4=60.4)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Primers PCR
Suggestions for RT-PCR validation
F:
No suggested primer sequences
R:
No suggested primer sequences
Band lengths:
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]