Special

HsaINT0086711 @ hg38

Intron Retention

Gene
ENSG00000164659 | KIAA1324L
Description
KIAA1324 like [Source:HGNC Symbol;Acc:HGNC:21945]
Coordinates
chr7:86891724-86893100:-
Coord C1 exon
chr7:86892922-86893100
Coord A exon
chr7:86891890-86892921
Coord C2 exon
chr7:86891724-86891889
Length
1032 bp
Sequences
Splice sites
5' ss Seq
AAAGTAAGT
5' ss Score
9.72
3' ss Seq
TTTATTTTATCACTATTTAGACT
3' ss Score
6.17
Exon sequences
Seq C1 exon
GAAACCTTGTATGTGTGGAATGAACCTAAATGGTGCATTAAAGGAATTTCTTTGCCTGAGAAAAAGTTGGCAACCTGTGAAACGGTTGACTTTTGGCTGAAGGTGGGAGCCGGTGTGGGAGCTTTTACTGCCGTTTTGCTGGTGGCTCTGACCTGCTACTTCTGGAAAAAGAATCAAAA
Seq A exon
GTAAGTACCCTCTGAGATGATCACAAGAGAGCTAGAGGGCCTATTTTGTTGTGAAAATTCTAGACTTGATCATTATATCCAATAAATAGATTCTCTCAGAGACACAAGAATTTTCTCCTTGCGAAGAAATCATAGGAAAGGCCTTGAGAAAGCAAGCAGAGGAAACGATTGTTATTCTGACAGTAGAAAGATCATAGAACATTAGAGATCATTGAGTTAGAGTCATTTATTAGAAAACAAGGAAAACAAGAGGCTCCATGTTATTCAGGTAGATGATAGCAGAGCTGAGATTTGGAAGGCAGGTATTCTCTCAGTGTCTGCCTTTTTTAAAAATGATATAATGCTGTCTTCTTCCTTCACCTTTTCTTTTAAAATTTCTTGTGGGAAGACATTTGCAAAAAAAACCAGACCTAGTGTATAGGCAAATATCACATTTATTTACTCCAGGTCTTCAAGTATCTGGAATTGAATATTGAGCCTAATTCCTGAATGTATTTTGATCTCTTATAGGACTTGAATCTTTTAGAATGATTTACACCTCAGTGGGACTGTGGAACTCCTATATTGTAATATCTAGGGACAATTGCAATATCTGGGGTGATAGTATAAAGGAATAAATAATATAGAGAGATGATAAAGACCAAATTACTTGCCTGTTTGATATTCTCATCTTTACGAACTAAATACTGGGAAAACCTTAGTGAATTGGCTTCCAAATATTCATGTTAAGAAAATGCATTCAGGCCTAAAAGTCCCTGCCCCCCAATTTTTTCATTATTGGACAATTCAATGTAAAGTGGTAGAATTAACTCTATTGAACTGATTTCTGACATCCTGGGAAATATTTCTTTGTAAATGGTAGATACATGATAACACACATATTGCTATGGCTATAGGCTAGGGAAATTTGTTGGTGGAGCAATTATACTCCAAGTCAATTTAATGAGCTGGTATATTACCACCTAAAATAAGTATTTATTTATATTAACATAAATGGATACTTATTTGTTTATTTATTTTATCACTATTTAG
Seq C2 exon
ACTGGAATACAAATATTCCAAGTTAGTAATGACGACTAACTCAAAAGAGTGTGAACTCCCGGCTGCAGACAGTTGTGCTATCATGGAAGGAGAAGATAATGAAGAGGAAGTTGTATATTCCAATAAACAGTCACTACTAGGAAAACTCAAATCTTTGGCAACCAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000164659:ENST00000450689:20
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:
ACCTTGTATGTGTGGAATGAACCT
R:
CTTGGTTGCCAAAGATTTGAGT
Band lengths:
342-1374
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