Special

HsaINT0086706 @ hg38

Intron Retention

Gene
ENSG00000164659 | KIAA1324L
Description
KIAA1324 like [Source:HGNC Symbol;Acc:HGNC:21945]
Coordinates
chr7:86908447-86910001:-
Coord C1 exon
chr7:86909812-86910001
Coord A exon
chr7:86908544-86909811
Coord C2 exon
chr7:86908447-86908543
Length
1268 bp
Sequences
Splice sites
5' ss Seq
TAGGTAAGC
5' ss Score
8.89
3' ss Seq
TCTTTTTAAATGTCATCTAGGAG
3' ss Score
7.44
Exon sequences
Seq C1 exon
GGGAAGAAGATGGCTCTCTGTACCAACAATATAACAGACTTTACAGTAAAAGAAATAGTGGCAGGGTCAGATGATTACACAAATTTGGTAGGGGCATTTGTATGCCAGTCAACAATTATTCCTTCTGAAAGTAAGGGTTTCCGAGCAGCCTTATCATCACAATCCATCATTCTGGCAGATACATTCATAG
Seq A exon
GTAAGCTTCCTTTGGTTCATATATGCATGCATACATTTATTCTTAAATTATGCTATGAATAACTTGTCATTGTATTGGTGTTTGCTATAGATGATTAAGGCCCCCACAGGTAATTTTAAATTGTCACTTTGTAAGATGGTTAAAAAGCTCCTACTAGTGGGGACTATTGATTAGTCTCTGAGAAGCTTCTGCATTTATGTATTAATTCATATATAAGTATGACATTTTCTGAGGGTCTATGCCTGTCATCAGACTTTCTAGAACTTTAAGAGGCAAACCAATTTTAAAAATCAAAACTAAAAACAAAATAGGAATAGTAAACAAACACAACTACACCTAAATTATTTATATGCCACCAGTTTCCATCACCTTTTCTCATACCAAAAGGAAGCAGGTGACAAACAGCAAAGGTGAGGGTGCTGAGTTTGATTCCTCATGTTCCCTTTTTGTCTCTGTAGTCCTGGAGGTCATAGATAAGTTTCAAGAAGAATCTAGCTCTCTAATGGGTGATTCTTAGGGATCAAATTTATTATGATCTCTACAGTGGGGCTTAGGAATCTGTGGTTTTAACAAGCTTCATAGGTGATTCGGATGTGTGGCCAGATTTGAGAACATTGCTTATAGTATAGACTCCAGAGGAATTTAGCATTGACTTTCAGCACCAAGGTCAGTTACTGGGGTGGGGGTTGCTCAGATTGGGAACTCTGAAGCAAAGTTTGCTCTTATTGTGTTTTGGCTCTGTTATTTTGCTTACAAGAGGCAGGGAAAAAAAGCCTTAGTTTTCTGCTTACTAGATTAAGCAAATTTCAGAGTTATTTTCTGGAAATTATTAGGGCACAAAATTTTTTGCTTTGTCAAATATGTCTATATTGAATATGAGTAAAAAGCTGTATTAGCAAAGTAGCCTAACTCATTCGATAAAATTCACTGGAGAATGAAAATTTTAATAGACTTTTGAGATGTTAGAGAACTGAAACGAACTTCGTAGATTATCGAATTACTGCTTGCATTAGATTCAGGCAACAAGACCCAGGGAAGTGAAAAGACTTAAGCAAAATTACAAAACTAGGGAGTAGAATCTTTTCTCTTTCATTCTGGAGACTTTGGAAAATTTCTTGTTTTTACCATGAATGCATTAATATAATACAGCATTTCTGTAAATATTGTAAAATGACAGTCATTAAAGCTATTTTCTATTCAAAACTACGGAGACCAAATAAAACTAATTTTCCATATTGCTTAATAGTTTCTTTTTAAATGTCATCTAG
Seq C2 exon
GAGTCACAGTTGAAACCACATTGAAAAATATTAATATAAAAGAAGATATGTTCCCAGTTCCAACAAGCCAAATACCAGATGTGCATTTCTTTTATAA
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000164659:ENST00000450689:16
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
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GGGAAGAAGATGGCTCTCTGT
R:
AAATGCACATCTGGTATTTGGCT
Band lengths:
278-1546
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