HsaINT0086690 @ hg38
Intron Retention
Gene
ENSG00000116299 | KIAA1324
Description
KIAA1324 [Source:HGNC Symbol;Acc:HGNC:29618]
Coordinates
chr1:109200059-109200900:+
Coord C1 exon
chr1:109200059-109200237
Coord A exon
chr1:109200238-109200734
Coord C2 exon
chr1:109200735-109200900
Length
497 bp
Sequences
Splice sites
5' ss Seq
AAAGTACAT
5' ss Score
1.57
3' ss Seq
CCCATCCTCCTGTTTTATAGACT
3' ss Score
7.96
Exon sequences
Seq C1 exon
AAGACTACTTACGTGTGGCGAGAACCCAAGCTATGCTCTGGTGGCATTTCTCTGCCTGAGCAGAGAGTCACCATCTGCAAAACCATAGATTTCTGGCTGAAAGTGGGCATCTCTGCAGGCACCTGTACTGCCATCCTGCTCACCGTCTTGACCTGCTACTTTTGGAAAAAGAATCAAAA
Seq A exon
GTACATGTTGCGGTATTGGAGTGTGGGGATGGACAGGGTTGGATTATTGATCAGGGAGAATATCTGAAAGTATAAATTAATGGGGTTTTTCTCTGGAGTTGGCTACAGACTCTGTGACTTATCCAGTGCATGGTTTGGTTATCCTGACTCCTGAACAGGGATGGTACCACGTGGCAGTCTATAAATGGATGTTAAATTCTCAAAAGCAAAGAGTATCCTCAGTTTGCTATTATTAACAGTACAGAGAATGACATTATGATTTTGATATTTCCATTAAATTTTGAGATCATAGAAACAGACAGCCTTAAGGAACAAAGATCACTGAACTGGGAACTAAGATTCCTTCTATTACCCCAGCCCTGACACCATTTTACCATGCTTCAGTCTCCTTACCCATGGCATGGGAATAGGACCTGTTCATAGCCTAACCTCTCTACCTCTTTCCCCCTTATTCCCACATTTTGGGATCTTGTCTTTCCCATCCTCCTGTTTTATAG
Seq C2 exon
ACTAGAGTACAAGTACTCCAAGCTGGTGATGAATGCTACTCTCAAGGACTGTGACCTGCCAGCAGCTGACAGCTGCGCCATCATGGAAGGCGAGGATGTAGAGGACGACCTCATCTTTACCAGCAAGAAGTCACTCTTTGGGAAGATCAAATCATTTACCTCCAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000116299:ENST00000369936:12
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:
NO
A:
NA
C2:
NO
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:
AGACTACTTACGTGTGGCGAGA
R:
TGGAGGTAAATGATTTGATCTTCCCA
Band lengths:
342-839
Functional annotations
There are 0 annotated functions for this event
GENOMIC CONTEXT[edit]
INCLUSION PATTERN[edit]
SPECIAL DATASETS
- Autistic and control brains
- Pre-implantation embryo development