HsaINT0151626 @ hg38
Intron Retention
Gene
ENSG00000115840 | SLC25A12
Description
solute carrier family 25 member 12 [Source:HGNC Symbol;Acc:HGNC:10982]
Coordinates
chr2:171809606-171810276:-
Coord C1 exon
chr2:171810224-171810276
Coord A exon
chr2:171809687-171810223
Coord C2 exon
chr2:171809606-171809686
Length
537 bp
Sequences
Splice sites
5' ss Seq
ACTGTAAGT
5' ss Score
8.59
3' ss Seq
GATGTTGTCTTTCTAATTAGGTT
3' ss Score
10
Exon sequences
Seq C1 exon
GTCTGATACCACAACTTATAGGGGTTGCTCCAGAAAAGGCCATTAAACTGACT
Seq A exon
GTAAGTTTATCTCTAACTGAATTTATGTCATTTGTTTAGATTACCATTAAGCCAAAAAGCTAAAATCAAGGCTAGGCGTGGTAGCTCATGCCTATAATCTCAGCATTTTGGGTGGTGGGAGGATCACTTGAGACCAGTTCTAAACCAGCATAAGCATAGTAAGAACTCAGCTCTACCAAAACAACAACAACAACAACAAAATTAAAAATTAGCCAAGTGTGGTGATTTATGCCAGGAGGCTGATGTGGGAGGATTGCTTGAGTCCAGGAATTTGAGGCTGTAGTGAGCTATGATCATGCCACTGCACTCCAGCCTGAGCAACAGAGTGAGACCCTGTCTCAAAAACAAAACTAAAATTGATGCTGCTGACACTGGCACACTGTCGCAGAATTTGTACAACTTTAATTTTACATGTAAGCATTTGATAATTTTAAATTTTATCATAAGACAAATATTTTGCTGACTTGGAAAAGCAACAGTATGCCAGAAGAGAAATGGTTGGGAATTTTGGTTAACTGATGTTGTCTTTCTAATTAG
Seq C2 exon
GTTAATGATTTTGTTCGGGACAAATTTACCAGAAGAGATGGCTCTGTTCCACTTCCAGCAGAAGTTCTTGCTGGAGGCTGT
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000115840:ENST00000422440:12
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=FE(17.3=100)
A:
NA
C2:
PF0015322=Mito_carr=PD(12.2=44.4),PF0015322=Mito_carr=PU(14.1=48.1)
Main Inclusion Isoform:
NA
Other Inclusion Isoforms:
NA
Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Fruitfly
(dm6)
No conservation detected
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