Special

HsaINT0151740 @ hg38

Intron Retention

Gene
ENSG00000125648 | SLC25A23
Description
solute carrier family 25 member 23 [Source:HGNC Symbol;Acc:HGNC:19375]
Coordinates
chr19:6453981-6454475:-
Coord C1 exon
chr19:6454323-6454475
Coord A exon
chr19:6454089-6454322
Coord C2 exon
chr19:6453981-6454088
Length
234 bp
Sequences
Splice sites
5' ss Seq
CAGGTGAGG
5' ss Score
10.07
3' ss Seq
CCTGTGTCTCCCCGCCTCAGATC
3' ss Score
9.86
Exon sequences
Seq C1 exon
GTCCATGCCTCAAAGACCAACCGGCTGAACATCCTTGGGGGGCTTCGAAGCATGGTCCTTGAGGGAGGCATCCGCTCCCTGTGGCGCGGCAATGGTATTAATGTACTCAAGATTGCCCCCGAGTCAGCTATCAAGTTCATGGCCTATGAACAG
Seq A exon
GTGAGGGCAGGTACAGGGAGGAATGTGCTTGCCATAGGGAAGACTGGGCTGTACATAAAGATTTACGGGATTGGCTTGGGGGTGGGTGGTGAACACAGGTCCCCAGGATCAGGCATCTGCTCCTCTGCATGAATGCCTGCAGCAAGCCAGTTCTTTGGAAGCCAGGAGAACAGTGGAGTGCAAGGAAGGTTCAACCCCCATGGTCCTACCCATCCCTGTGTCTCCCCGCCTCAG
Seq C2 exon
ATCAAGAGGGCCATCCTGGGGCAGCAGGAGACACTGCATGTGCAGGAGCGCTTCGTGGCTGGCTCCCTGGCTGGTGCCACAGCCCAAACCATCATTTACCCTATGGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000125648:ENST00000301454:6
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(73.0=96.4)
A:
NA
C2:
PF0015322=Mito_carr=PD(24.3=24.3),PF0015322=Mito_carr=PU(28.0=70.3)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
TCCATGCCTCAAAGACCAACC
R:
CTCCATAGGGTAAATGATGGTTTGGG
Band lengths:
260-494
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains