Special

HsaINT0086705 @ hg19

Intron Retention

Gene
ENSG00000164659 | KIAA1324L
Description
KIAA1324-like [Source:HGNC Symbol;Acc:21945]
Coordinates
chr7:86539128-86541561:-
Coord C1 exon
chr7:86541388-86541561
Coord A exon
chr7:86539318-86541387
Coord C2 exon
chr7:86539128-86539317
Length
2070 bp
Sequences
Splice sites
5' ss Seq
GAGGTGAGT
5' ss Score
10.03
3' ss Seq
TTATGACTTTATTTTCCTAGGGG
3' ss Score
7.56
Exon sequences
Seq C1 exon
GACCATTCGGTTTGCTATAGTGACTGCTTTTTCTACCATGAAAAAGAAAATCAGAGTTTGCACTATGACTTTAGCAACCTCAGCAGTGTGGGCTCATTAATGAATGGCCCCAGCTTCACCTCCAAAGGAACAAAATACTTCCATTTCTTCAATATCAGTTTATGTGGGCATGAG
Seq A exon
GTGAGTTCTGGCTGTCAAGGTGAGATGGACCTATATTTCAGCTCCGATCAAGTTGATATTTTCTGTGTTAATGGACCAATAAATTCTCTATGGATATCAACCAAGTGTCAGAAACTGAGGTTTGATTGCTTAGATCCTCTATTGCTGCCTAGAATATTGGCAGATTTCTCCACCAGGGGCAACCTTGTCTGGTTCTCAGTGTATCAAATCACTTATGCAGTCAGTTGAAACCTGAAGCTTGGAGCTATGGTGTAAGTGCTTTGAGGATGTTTTGTTTTCATAAAAATGGGTCAGGGTTGTCAATCTTACCTCTTTAGGCAGGAAGTTATTTGAGAAAGTTTTACTGTTGTTTATGTTGTCAATTTTGTGTTTTAAGAAGAAAAAGACTTTCAAGAGGAAGCTTGTCCAAAATAAAAAGGAGACATGCAGGGCCAAATATCAGTTGATAAGGTAGGCTTAAATCATACAAATGGGATTTTATTTGCTGTGAGAAGAAGAGGAATCTTAATTGATACTGGCAATGGGGAGAGGTTACAGGACCATGATGCCCAATATTTTAATGGACATATGAGGTTAGGGTTGGGAAGTATGTATAGGTATATACCTACAGAGTAGGAACAGGATAAGGCATTTCCTCCATGTCACTTCCCATATTAACTCCTATATTTTCAATTGTCTTCATTATGAGATACTGTGCAAAGCTTTGAACAAAGGAAACAAAAAGAGATCTGATGACCACAGAAGTTTTCAAACAAAAAGATCCATAAAATTTTACATAGTATGACAGCTGTCCTGTTTTGATTTTACCTGGGGTGATCCAAGACACTCACTAGATTGGTTACTCAGTTCACTCAATAAATATAAATTAAATACCTGTTATGTGCCAGATACTGTGGGAAGCAGTGAATAAGATTAATTCCATTGTCTACCATACTTCTATCACAATCTTATTGTACATTAGCACTACCTCTTTTTCCACCTTCTCTTCTCTTCACCTCTAGCTTCTATCTCTTTCCTTCCTTTTTATTCTTGTTTCTTTCCTTTTAGCTTCCACTATTTTCCTTTTTCTTTCCCCAGTACCTTTTCTCTGATCTTTTCCATTATTTTTTATTGGCTTCAACATTTTAATTTAAGCCTAGTAAAAAAAATATACTGGTGAGAAGGCCTATTGTCAGAAGGCCTGGTAGCAGGAGAAAAATTTATAGGTTAGGTCTGCTAGCTGCATTAAGAAAGATAAACTTTTATACTTTTCTTTTTACACATCTGTGTACACTCTATATCTAACACCAATGAAATAGTTTTCCTGTATTATTTTTACATTTACTTTGTAGAAATTATGGAGCAAGCTATAGTCTTTTGCAGTAGGACTACAGTAAATTTAAACATATTATATTTAAACAATTTTTCCATTTTTTATAAGTTATATCTTCCAATTATTTTCAAAATTATTAAAAAAGCTAATCTCTCTATTACCTTTAACTTGTTATACAGTTGAACAGATACACATCATTGAAACTAAGAGTAGGTTAATAAAGACACTTGTAGTGACCAATTATTTAGAATTCAGGTGTTATTCTAGAATTTTGCTGCAGTATGACTTTTGTGCTTTCTTCTTTAGCCTTCACATTACCTTTCTGCTACACATAGGGTCATAAAGGAAAAGGAAGACCAACACTTTTTCTTTGACACTGAAGCTTTCATCAGCAGTTTTCTGGTCTTTTTGCATGCATTGTTACTCTATGAATTGAACATTTCATAGATTACTTTTATTTTCTCAAGTTTGATGACTTTCATTTATCACAAATGATGCTTGTACTGGGAAGAGCAGTATAGTCTTGAATTACTGTATTTGTTATAACTGTAGACTCTGAAGTTTGGTTGAATATTGGACTTTCCTTGAGAGCTTTTAAAAAGTACTGATGGGTGGCTAGGCCTCATACCAGATCAACTAAATCAGAATCCTTGCAGTGAGGAGAGAGCCACTGCTCTTCTAGGGTCACTAGCTAGTCAAGATTAAGTTTAGAGATTGACATCCAATAAAACCTTTCTTTTATGACTTTATTTTCCTAG
Seq C2 exon
GGGAAGAAGATGGCTCTCTGTACCAACAATATAACAGACTTTACAGTAAAAGAAATAGTGGCAGGGTCAGATGATTACACAAATTTGGTAGGGGCATTTGTATGCCAGTCAACAATTATTCCTTCTGAAAGTAAGGGTTTCCGAGCAGCCTTATCATCACAATCCATCATTCTGGCAGATACATTCATAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000164659-KIAA1324L:NM_001142749:15
Average complexity
IR-S
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=PD(15.7=13.8)
A:
NA
C2:
PF129842=DUF3868=PD(1.5=8.3)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
No suggested primer sequences
R:
No suggested primer sequences
Band lengths:
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