Special

HsaINT0151741 @ hg38

Intron Retention

Gene
ENSG00000125648 | SLC25A23
Description
solute carrier family 25 member 23 [Source:HGNC Symbol;Acc:HGNC:19375]
Coordinates
chr19:6452312-6454088:-
Coord C1 exon
chr19:6453981-6454088
Coord A exon
chr19:6452480-6453980
Coord C2 exon
chr19:6452312-6452479
Length
1501 bp
Sequences
Splice sites
5' ss Seq
GAGGTGAGA
5' ss Score
7.66
3' ss Seq
GATAACCAGGTTCTCCCCAGGTG
3' ss Score
3.7
Exon sequences
Seq C1 exon
ATCAAGAGGGCCATCCTGGGGCAGCAGGAGACACTGCATGTGCAGGAGCGCTTCGTGGCTGGCTCCCTGGCTGGTGCCACAGCCCAAACCATCATTTACCCTATGGAG
Seq A exon
GTGAGAAGGAGGGACCCCAGCGGAGGCCCCATGGCAGGGTGGGGGGCCTGCTGTACCCATCTCACTCTGCATTTCACAATATCCATTGGGATTTTACCTTTGTCCCTCTCTGATTTGGAGTATAGCTCATCAGAGTAATGCAATTTCATGTGTAGCCTGTCTGGGTATTACAACTGAGATATAATTTCTGGGGAAGGTAGTGTCGGTTATCCTTGTTTGGATGGTAGTCATAGGAGCCAGCTGTTTATAAATATGCATCTTCTAAGGATAGGGTGCACGTTCCCAGGGACGTCGTGTCTAGGTGTCACCAACTGTTTATGAATATGCCTCTTCTAAGGATAGACTGTGCTAGCTACATGTTTTCAGATAAATTATTTCAGGTTTCAGGTTATGAAGTGTATTGTTTGGATTCTGAAAGTGACAGAAAACTTAAATCATGTCAGCTGGGTGCGATGTCTAGCGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGTGGATCACCTGAGGTCAGGAGTTCAAGACCAGCCTGACCAACATGGTGAAATACCGTCTCTACTAAAAATACAAAAATTAGCTGGGGATGGTGGTGGGCACCTGTAATCCCAGACACTTAGGAAGCTGAGGCAGGAGAATGGCTTGAACCTGGGAGGCGGTGGTTGCAGTGAGCCAAGATCATGTCACTGCACTCAGTCTGGGCAACTGAGCAAGACTCCAGCTCAAAAAAAAAAAAAAAAAAACTTCAATCACATCAACAAAGTCTACAGATGAGCATTTCAGGCTGGGATGGTAGCTTCAGAGTGTTAGCGATGCAGGTTCTTTCTGTCTATCTTGTTGTTACACAACCTCATGGACCAATGTGGCTGCTTGTGCTCCGTTCATCACATTCCACACTCCAGCCAAGAAGGAAGAAGCAATAAAAAAGGAAACACCTCCCCACCTCTAAGGATGCTTTCTGAACCTTATGTGTACCTCTTTCTCTTCCTTCTATTTCTTTGGCTAGGACATAGTGACATAGCCACATACCCAGGGCATCTGGGAAATGTCATTTTTCTTTCTAGTGGCTGTGTGCTTGCTGAAAGTTACAGTTTCTGATATGAAAGCAGAAGGGAACAAGATACTGGAGGTCTGGGCATGATGGCTCATGCCTGTAACCCCAGTCCTTTGGGAGATGGAGAGGGGAGGATCACTTGAGCCCAGGAGTTCGAGACCAGCACGGGCAAAGTAGCGAGTCCCCATCTCTACAGAAATGACCAAAAAATAAAAGAAAGATATCAGGAGACAGTTACTGGTGGTGCCACATGTGTGCACTTTGGTAGGTGTAACTATTTCTAGGTATAGGGATTTGGGGATAGCAGAAGATTCTAGAGTAGGTGGTTTTTAAAATTCGGTTGTTCTCAGGGCATCTGTTTTCAGGAGTAGCTATTTCTAGGTGTCTTCATTCCTGGATGTAGCGATTTGGTGGGACAGCTTTTCCAGGGATAACCAGGTTCTCCCCAG
Seq C2 exon
GTGCTGAAGACGCGGCTGACCTTGCGCCGGACGGGCCAGTATAAGGGGCTGCTGGACTGCGCCAGGCGTATCCTGGAGAGGGAGGGGCCCCGTGCCTTCTACCGCGGCTACCTCCCCAACGTGCTGGGCATCATCCCCTATGCGGGCATCGACCTGGCCGTCTACGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000125648:ENST00000301454:7
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=PD(24.3=24.3),PF0015322=Mito_carr=PU(28.0=70.3)
A:
NA
C2:
PF0015322=Mito_carr=PU(69.4=96.2)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
CCATCCTGGGGCAGCAGG
R:
CGTAGACGGCCAGGTCGAT
Band lengths:
264-1765
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains