Special

HsaINT0086685 @ hg38

Intron Retention

Gene
ENSG00000116299 | KIAA1324
Description
KIAA1324 [Source:HGNC Symbol;Acc:HGNC:29618]
Coordinates
chr1:109197474-109198075:+
Coord C1 exon
chr1:109197474-109197654
Coord A exon
chr1:109197655-109197978
Coord C2 exon
chr1:109197979-109198075
Length
324 bp
Sequences
Splice sites
5' ss Seq
TTGGTGAGT
5' ss Score
9.27
3' ss Seq
TAGGAGCTCTAATTTGGCAGGGG
3' ss Score
0.71
Exon sequences
Seq C1 exon
GGTAGGAAAATGTCTGTGTGCACCGACAATGTCACTGACCTCCGGATTCCTGAGGGTGAGTCAGGGTTCTCCAAATCTATCACAGCCTACGTCTGCCAGGCAGTCATCATCCCCCCAGAGGTGACAGGCTACAAGGCCGGGGTTTCCTCACAGCCTGTCAGCCTTGCTGATCGACTTATTG
Seq A exon
GTGAGTAACTCCGCTGCCTCAGCCTTGTTTGAGAGTGTGTGTGTGTGTGTGTGTGTGTGTATGTGTAAGAGAGTGTGAGGTTACCAGTCTGGGAGGTAAAAGGCCCCACATGAGGGGCCCAACCTCTTGACCTGTGTTTTCTATTCCACTCTGTGTGCAAAGTGCTCCCAGGGACTCTGACAAACCCTTGTTTCACCCTTTCATAAGCCACTCAGGGATGTGATGAGATGAAGTGAGGTTGGATGTTGACAGGTATTGGAAGAATTGAAGTGGTTGCCAGCTAATGCTACTAGTGAGAACTAATTAGGAGCTCTAATTTGGCAG
Seq C2 exon
GGGTGACAACAGATATGACTCTGGATGGAATCACCTCCCCAGCTGAACTTTTCCACCTGGAGTCCTTGGGAATACCGGACGTGATCTTCTTTTATAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000116299:ENST00000369936:8
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


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
GGTAGGAAAATGTCTGTGTGCAC
R:
CTATAAAAGAAGATCACGTCCGGT
Band lengths:
278-602
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