Special

HsaINT0151739 @ hg38

Intron Retention

Gene
ENSG00000125648 | SLC25A23
Description
solute carrier family 25 member 23 [Source:HGNC Symbol;Acc:HGNC:19375]
Coordinates
chr19:6454323-6454717:-
Coord C1 exon
chr19:6454559-6454717
Coord A exon
chr19:6454476-6454558
Coord C2 exon
chr19:6454323-6454475
Length
83 bp
Sequences
Splice sites
5' ss Seq
CAGGTGAGG
5' ss Score
10.07
3' ss Seq
GCTGTTGTCTCCCCATTCAGGTC
3' ss Score
10.79
Exon sequences
Seq C1 exon
GTCCTGGACATTGGCGAGTGCCTGACAGTGCCGGACGAGTTCTCAAAGCAAGAGAAGCTGACGGGCATGTGGTGGAAACAGCTGGTGGCCGGCGCAGTGGCAGGTGCCGTGTCACGGACAGGCACGGCCCCTCTGGACCGCCTCAAGGTCTTCATGCAG
Seq A exon
GTGAGGGGCTCTGGAGAGACCTGCCCCCTCCCCCAGGCCTGACACCTGGGAGGGGACCTCCAAGCTGTTGTCTCCCCATTCAG
Seq C2 exon
GTCCATGCCTCAAAGACCAACCGGCTGAACATCCTTGGGGGGCTTCGAAGCATGGTCCTTGAGGGAGGCATCCGCTCCCTGTGGCGCGGCAATGGTATTAATGTACTCAAGATTGCCCCCGAGTCAGCTATCAAGTTCATGGCCTATGAACAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000125648:ENST00000301454:5
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:
PF0015322=Mito_carr=PU(34.4=60.4)
A:
NA
C2:
PF0015322=Mito_carr=PU(73.0=96.4)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
AAAGCAAGAGAAGCTGACGGG
R:
CTCCCTCAAGGACCATGCTTC
Band lengths:
182-265
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains