Special

HsaINT0086716 @ hg38

Intron Retention

Gene
ENSG00000164659 | KIAA1324L
Description
KIAA1324 like [Source:HGNC Symbol;Acc:HGNC:21945]
Coordinates
chr7:86938808-86940115:-
Coord C1 exon
chr7:86940010-86940115
Coord A exon
chr7:86938961-86940009
Coord C2 exon
chr7:86938808-86938960
Length
1049 bp
Sequences
Splice sites
5' ss Seq
AAGGTATTT
5' ss Score
7.64
3' ss Seq
TGTTTTTCATTACTGCACAGGGG
3' ss Score
7.17
Exon sequences
Seq C1 exon
GTAATGCTGAAATCAGGCACAAACATACTCTACTGGAGAACTACAGGCATCCTTATGGGTTCTAAGGCGGTCAAGCCTGTGCTGGTAAAAAATATCACAATTGAAG
Seq A exon
GTATTTCATGGCATTCTGTTTTAGTAGTCACCAGTCACATCTTACAGTTAGTTAAAATATTTATTAAAGTTTTGGTTTGGCTGGCTCAAAGATTTATAGAACAGAAATTAATATGTTAGGGAATCATATAGGTCTGGAGACCCTGGTTTTACTCCCAAGAAATCGACAGTTGTTTTCTTTTTTTCTTGTACCCTTGAACTAAATTATTTAATCATTGCAAAAAAAGTAAACATGATGACAATTTTAGATGTCTGTAAACAAAAACAAAATGTCTCTGTGTTAATAAGACCCCATTATTCCTCCAAGAAATGTCTGTTGTGCCAGACATTGGGCTTACCAGGGAACTGATGACCTAGTCACTGCTATATCCATAAAAATAACAATAAACATCTTGACCTGACTCTTTCCTAAACCTTTTATGCTTCTCTGAGCCAACCGGGTAATTTCTGGCCCAGGAGAGCAGTCGGTGAACCCTGGCATGGTTCATTCTCAATTAGGAGTATTTTTCATTAAAGCAGTGATTCTCCTTTATTAAACTTTGGCTTACGTTTTAATATGTTCATTGTGGGCTTGTTCCTGTGAACAATGTGTTAACTCATTAGTCACTAGGACATCTGCTGGCAAAGACTGGAATTACAAACCAGAGGAGAAGTCAAGCCATTCCTAGGTCTTACCTGTGACTTAATAAGCAGTGGAAAAAAAAGGGAACAGGTTACCATAAGGATCAGATAATTATAGCCCTATAGAATTGGAGGGAACCTTAGGGTTTATCTCATTTTTGAGTTAGTGGAGTTGTCTTTTGACTGCTCAGTTAATACAAGTATTATACCTCTATGAAATCTTCATCTCTTATTTGTTTGCTGACTTGATTGTGCAGTTCCTTGTACACAATAAATGCTTTCTTAGTGCTGGATGAATAAGATAAAAGATTTGGGCTGACCTTACTGTTCATATATCTCCCTCACTTCTGGGTAGAAGCAGAAGTAGGTGCTGATTTGCTTATTGGTATTGGGTCCCCCTCCCATGCTCTGTTTTTCATTACTGCACAG
Seq C2 exon
GGGTGGCGTACACATCAGAATGTTTTCCTTGCAAGCCAGGCACATTCAGCAACAAACCAGGTTCATTCAACTGCCAGGTGTGTCCCAGAAACACCTATTCTGAGAAAGGAGCCAAAGAATGTATAAGGTGTAAAGACGACTCTCAATTTTCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000164659:ENST00000450689:6
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:
PF076998=GCC2_GCC3=PU(0.1=0.0)
A:
NA
C2:
PF076998=GCC2_GCC3=WD(100=63.5),PF075629=NCD3G=WD(100=55.8)


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:
TGCTGAAATCAGGCACAAACA
R:
TGAAAATTGAGAGTCGTCTTTACACC
Band lengths:
254-1303
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