HsaINT0154551 @ hg38
Intron Retention
Gene
ENSG00000184347 | SLIT3
Description
slit guidance ligand 3 [Source:HGNC Symbol;Acc:HGNC:11087]
Coordinates
chr5:168722256-168723004:-
Coord C1 exon
chr5:168722933-168723004
Coord A exon
chr5:168722328-168722932
Coord C2 exon
chr5:168722256-168722327
Length
605 bp
Sequences
Splice sites
5' ss Seq
TCTGTGAGT
5' ss Score
7
3' ss Seq
ACATGCCTCCTTTTCCACAGGAT
3' ss Score
10.43
Exon sequences
Seq C1 exon
TGACCTGAGCAACAACAGCATCAGCATGCTGACCAATTACACCTTCAGTAACATGTCTCACCTCTCCACTCT
Seq A exon
GTGAGTACACTGAGATGCTGTGTTTACCATGCCCTTGGGCCTAGCAGTAGATGGTTACTCTTTCCCTCCCTCCCAGCAGGACTAGTTTCTCTGCCCTAATGACCCTCAGGCCTATGGCTGCCCTAGCATAAGATACACCTTAATCATCAGAAGGAAGATAAAGTAGGAAGCCCTCCACTGTCCAGGCAGTTAGAGAGGAACTAGAACCTCGTCGCTTCTGAAGAAGGCTGTCTTAGGAATACCTTTTGTGGTTTGTGAATTTTCTTTCCCGGAAATGGTTTTCCTACACAATTATATTTTGCTCACACCCATTTATTTCCCATTAGCTTTACACATTGTGAGTACTCATCATTGGACAGGAGAGAGAGGTGACGAACAAGCTGGTTAGAAAGCCAGCCTGCCACAGAACTTGAGTAAACTGAGGAAATAAAGCCAGTGCGCTTCCTGGATTGGTGAAGAGGTTTCTTGTCCCTTTAGGGGATGTTCTGTCAATATATCAACATTGAAAAGATAAACCATTTGCTTTGTTTCACAACGTGAACAGTGCACCTATGCATGGTAGAGAATAGAAAGACACAACAGGGCACATGCCTCCTTTTCCACAG
Seq C2 exon
GATCCTGAGCTACAACCGGCTGAGGTGCATCCCCGTCCACGCCTTCAACGGGCTGCGGTCCCTGCGAGTGCT
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000184347:ENST00000519560:22
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:
PF127992=LRR_4=PD(38.6=68.0),PF138551=LRR_8=PU(8.2=20.0)
A:
NA
C2:
PF138551=LRR_8=FE(39.3=100)
Main Inclusion Isoform:
NA
Other Inclusion 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