Special

HsaINT0151875 @ hg38

Intron Retention

Gene
ENSG00000181240 | SLC25A41
Description
solute carrier family 25 member 41 [Source:HGNC Symbol;Acc:HGNC:28533]
Coordinates
chr19:6427334-6429831:-
Coord C1 exon
chr19:6429724-6429831
Coord A exon
chr19:6427502-6429723
Coord C2 exon
chr19:6427334-6427501
Length
2222 bp
Sequences
Splice sites
5' ss Seq
GAGGTAAGA
5' ss Score
10.06
3' ss Seq
TTGTTCCCCGCCATCCTCAGGTG
3' ss Score
9.53
Exon sequences
Seq C1 exon
TGCAAGAATTACTTCTGTGGAATACAAGGGTCCCCGCCCTTCCAGGAGCGTCTCCTTGCTGGCTCCCTGGCTGTGGCCATCTCCCAGACCCTCATCAACCCCATGGAG
Seq A exon
GTAAGAGAGCATGTGCCCCGCAGGTGAGGAAACGCCGTGGAAACTAGTTACCCACGTTGCTGGGGCTACTTCCTCTTCCTCCTTTCTCCCCTCCTCCTTTCTCCTCCTTTTTTCTCACACTTCTCCCTCCTCCCCGTTCACCTCTTCCTCCTCTGTCTCCCCTCCTCCTTTCTCCCTCCTCCTCTTTCCTCCTCCTTTCTCCTTCCTCCTCTCCTCCTCCTCCTTTCTCCCTCCTCCTCCCCTCCTCTTTCCTCTCCTCCTCCCCTCCTTTCTTCCTCCTCCTTCCCTCCTCCTTTCTCCCTTCTCCTCCCCTCTTCCTTTCTCCCTTCTCCTCCCCTCTTCCTTTCCTTTCTCCCTCCTCCTTTCTCCCTCCTCTCCCTCTTCCCCCTTTACCTCTTTCTCCTCCTCTCCAATCTCCTCCTCCTTTCTATAAATTTATATATGAATATATTATATATAACACATATACATATATATAACATTTTCATAAATTTATATATGTATATATTATATACAACATATATATTATATATATAACATATATATATTATATATATATTATATATATAATATATATATTATATATATATATAACATATATATAATATATATATTATATATATATGTAACATATATATAATATATATATTATATATATATATAACATATATATAATATATATATTATATATATATATATAAATTTTCAGGCCAGACACCTTGGCTCATGCCTGTAATCCCAACACTTTGGGAGACTGAGCTGGGAGGACTGCTTGCTTGAGCCCAGGAGTTTGAGACCAGCCTGGGCAATATAGCAAGACCCCATCTTTACTGAAAACAAAAATCAGCCAGGTGTGGTGGCGCATGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGTGGGAGGAGCACTTGAGCCCAGAAGGTCGAAGCTGCAGTGAGCTATGATGGGACACAACTGCACTCCAGCCTGGGTGATAGAGGGAGACCCTGTCTCAAAAAAAATATATATATATATATGTTTTATATATAATATACACATATATTATATACCTTACTTATTATGTAAATATATAGTACATATAACATGTATATATTATATATAACTAAATAATTTAATGTATCTAATTATATAATTACATTTATTATATACTATGTAATATAAAAATATGTCTATGCATGTTATATATAATATATGCATAATGTATAATAATACATATATAATATGTATATATACTATATATATGTATACATATATATTTTCATTTCTCATCTGTGGACCGGAAACCCTCCTTTTTTTCTTTCTTTTTCTTTTTTTTTTTTTTGAGAGTCTCACTCTGTCACCCAGGCTGGAGTGCAGTGGCACGATCTTGACTCACTGCTCACTGCGACCTCCACCTTCTGGGTTCAAGCGATTCTCCTGCTGGGATTACAGCTGCCTGCCACCACACCCAGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCGCCATGTTGCCCAGGATGGTCTCAAACTCCTGACCTCAAGTGTTCCACCCACCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCTACCGCACCCGACCTAGGGTTCACTCTTAATCTAACAGTTCTATGGGTTTTGAGGAATGTATAATGACTTGTATCCACCATTGTAGTATCTTACGGAGTAGTTTCACTGCCCTAGGAAGGCCCTGTTTTCTACCTATTCACTCTCTTTCTTTCCCCCCAGTGCTTGATCTTTTTGCCATAAAGTTTTGCCAGCTGTCTTCAATTTTTGAGGCTTGAGGGCATGTTTTCTCGCCTCCCTTCCCTGTTATTCTTAATCAGTTTTCCAGGCTGTTCTCCCATGTTGATGTTTCCATATACATCTTATTTTTATTTTATTGATTTTTTTGTAAAGATGGGGTCTCGCTATGTTGCCCAGGCTGGTCTCGAACTCCCGGCCTCAAGCGATCCTCCCGCCTCAGCCTCCCAAAGGGCTGGGAAGACAGACGTGAGCCTTCTTCCCTCACTCTCTTGGCCTTTGCCAGCATTTGTGCTTCAGAACTCAAAATTCAGAGAGCATTCCATGGAATCTGACAGATCCGGGTCTGAAACCCAGCTCTTTGCCTTCCTGAGCCTCATTTTCCTTGTTTGTAGGGTGGGGACAATGGCTACCCCGAGGGTCATTGACAGGATTCAATCAAATGAGCTGCCTTGTTCCCCGCCATCCTCAG
Seq C2 exon
GTGCTGAAGACGCGGTTGACCTTGCGTCGGACGGGCCAGTACAAGGGGCTGCTGGACTGCGCCAGGCAGATCTTGCAGCGAGAGGGCACCCGCGCCCTTTACCGCGGCTACCTGCCCAATATGCTCGGCATCATCCCCTATGCCTGCACCGACCTGGCTGTCTATGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000181240:ENST00000597558:4
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.083 A=NA C2=0.009
Domain overlap (PFAM):

C1:
PF0015322=Mito_carr=PD(7.5=19.4),PF0015322=Mito_carr=PU(28.0=72.2)
A:
NA
C2:
PF0015322=Mito_carr=FE(59.1=100)


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:
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]


SPECIAL DATASETS

  • Autistic and control brains