Special

HsaINT0151876 @ hg38

Intron Retention

Gene
ENSG00000181240 | SLC25A41
Description
solute carrier family 25 member 41 [Source:HGNC Symbol;Acc:HGNC:28533]
Coordinates
chr19:6427103-6427501:-
Coord C1 exon
chr19:6427334-6427501
Coord A exon
chr19:6427251-6427333
Coord C2 exon
chr19:6427103-6427250
Length
83 bp
Sequences
Splice sites
5' ss Seq
GAGGTATGG
5' ss Score
8.98
3' ss Seq
CTGGCCCCCTTCTCTTGCAGATG
3' ss Score
13.07
Exon sequences
Seq C1 exon
GTGCTGAAGACGCGGTTGACCTTGCGTCGGACGGGCCAGTACAAGGGGCTGCTGGACTGCGCCAGGCAGATCTTGCAGCGAGAGGGCACCCGCGCCCTTTACCGCGGCTACCTGCCCAATATGCTCGGCATCATCCCCTATGCCTGCACCGACCTGGCTGTCTATGAG
Seq A exon
GTATGGGTCCTGCAGAGGGGGTGGCAGGGCTGGCCGGAGCCCAGGCTCCTAGTGAGCTTTCTCCTGGCCCCCTTCTCTTGCAG
Seq C2 exon
ATGCTCCAGTGCTTCTGGGTGAAGTCAGGCAGGGATATGGGGGACCCCAGTGGCCTGGTCAGTCTGTCGTCTGTGACGCTATCCACGACCTGTGGCCAGATGGCCAGCTACCCACTGACTCTGGTGCGCACCAGGATGCAGGCCCAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000181240:ENST00000597558:5
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.009 A=NA C2=0.020
Domain overlap (PFAM):

C1:
PF0015322=Mito_carr=FE(59.1=100)
A:
NA
C2:
PF0015322=Mito_carr=PD(9.7=18.0),PF0015322=Mito_carr=PU(38.7=72.0)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GCATCATCCCCTATGCCTGC
R:
CACCAGAGTCAGTGGGTAGCT
Band lengths:
167-250
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Genotype-Tissue Expression Project (GTEx)
  • Autistic and control brains