Special

HsaINT0087356 @ hg38

Intron Retention

Gene
ENSG00000134313 | KIDINS220
Description
kinase D interacting substrate 220 [Source:HGNC Symbol;Acc:HGNC:29508]
Coordinates
chr2:8786206-8788812:-
Coord C1 exon
chr2:8788647-8788812
Coord A exon
chr2:8786358-8788646
Coord C2 exon
chr2:8786206-8786357
Length
2289 bp
Sequences
Splice sites
5' ss Seq
GAGGTGAGT
5' ss Score
10.03
3' ss Seq
GATTTGTTCTTTTCTTCAAGGTT
3' ss Score
8.64
Exon sequences
Seq C1 exon
TTGTCATTTACTTTGGTGGACGAAGAGAAGGAGAGAGTTGGAATTGGGCCTGGGTCCTCAGCACTAGATTGGCAAGACATATTGGATATTTGGAACTCCTCCTTAAATTGATGTTTGTGAATCCACCTGAGTTGCCAGAGCAGACTACTAAAGCTTTACCTGTGAG
Seq A exon
GTGAGTTGTACCATTTGACAGAAGAAATCTTCAATGAGATTCAGAAAAAAATATTTTTCACTTCGGAAAGTTTATAGGAGCCGGGTGTGGTGGCTCACGCTTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGCAGATCACCTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAATTAGCGGGGGCGTCATGGCGCATGCCTGTAGTCCTAGCTACTTGGAAGGATGAAGCAGGAGAATCGCTTGAACCTGGGAGGCAGAGGTTGCAGTGAGCCAGGATCGCGCCATTGCACTCCAGCCTGGGCGACAAGAACGAAACTCTGTCTCAAAAAAAAAAAAAAGTTTATAGAATATAATTTCTCAATGTATGTTCCAAAAAACATTGGAACCTTTTACATACAGAAATAAAAACATGCCCTGGTCAAATACCGTGGGAAACACTTCAGATTATATATCCCTCCTGTACGTTAAAGGATCAGAGGCACCTTTCCATAAAGAAACCTGTTTAACTTTTATTTACCAAATTTTATTTAAGCATAAACCTTTTCTCCCTGTTATGTCACCTGTTACCATCTTTTGGAACACACTTTGAAGAGAGCACTGGATGGAGGAGGGGTCCAGCCACTGGCCTTGGTCCCCAGAGAGCTTCCCGCTGGAGACCTGGCCCTTCCTTATGTGAGCGGTTAACCTGGGGAAACCCAGCTCCCCTCTCTGAGCTGTGCTTTTCTCAGCTCAGGAAATATATTCACATGTCTGTCTAAAATTATTATTCATATTAAGTAGGAAATTTATGAGAAAAAAGAAAAGATGAAAAATGTTTAAGTCCAGGAATAAAGGAAAGGTAGAGGGCTCCAGAGGACAGTGAAATGAAAAAAAAAAAAAGCTAGAAAGTTAAAAGCAAAAGAAATTCAATGGAAGTAAGCAATGTAAGAATTTAAAATGTATTAAGCCAGATGTGGTGGCTCACACCTGTAATCCCAGCACTGTGGGAGGCCAAAGTGGTCAATTGCTTGAGCTCAGGAGTTCAAAACAAGCCTGGGTAAAGGCAAAACCCCATCTCTACAAAAAATAGAAAAATTAGCTGGGTGTGGTGGTGCGTGCCTGTAGTTCTAGCTGCTTGGGAGGCTGAAGTGGGAGGACTGCTTAAGCTTCGGGGGTTGAGGGTACAGTGAGCCAAGATCACGCCACCGCACTGCAGCCTAGGTGACAAAGTGAGACCCTGCTCAAAAAAAAAAAGCATTAAAAGATGAAAATTTTTTAGTTATAAGAAAAAATAAGTGTAATTTAAGATGAAAATAAATAAGCCAAACCAGGTAAAATATTAAAACTGAGTATAAGAGAAAAATAAAGGTAAAAACTTTTAAGTAACTAGCATAGAGAATTAAGTATTAAGAAAAGGATTTAAAAGTGAAAAAGTTAAAAGGAAAACAGAATAAAATAATTGGGGGAATATTTTTACAGAAAATAAGGAAACCAGTCTAAATTAATGAGGTGGTATTTTTTTTTTTCAGTTAGAACAATTAAAGTAGCATCGTCAAGACCACACAGTATATTACAGATTGTATTCTGAGAGCAATGCTTATCTACTGGACTGAGATGAGAGTTTAATTTAGAGATGGAAGGGAGAAAGGAACTAACAGAAATAATAATGATTCAGAGACTCTGAATACAAATAATTCACTTAATTTTGAAGATCAATTGTGAAGAGAATATTTTACAACTATTTCTCAATCCCTGGTAGACGTGGAAGCTATAAATAAAATAAGCCATGCTAAAACTTGAGTTTTTAAATGGTATTACTGGGCTTGAAATTCTTTAATGACTGTAATTAATATTTTTTCAGGGTTAGAGTCTCTTTCGTTGGTGTTAGAAAACTTTCTTGTGCAACTCTTGGTGGCCACATCATGACACGTGTGTCACCTTTTAACCACTATGTCGTGAGATCTGTTGGGGTGTCTTGATACTCCACATCTAAGTTCTGGCGTAACTTTCCCCCGCCTGTCCTTAGTCAGAATTACTTTATATGGCCCTGCACATTTCACTTTTGTTACTGTTTTTTCCTAAGAAAAGTATGTAAGATTTTAGAAGTGGAAGCTACCTAATTACAAATTCTTTTCCCTCCTTGGAATTTAAAAAACAATATTTTGAAAGAGACAAAAAGAAAATAAAGGGTAAGTGATGCAAAGATGACATACATTGAAGTTATTTGTTACTTTAGATAATAAAGTAATGTTTGATTTGTTCTTTTCTTCAAG
Seq C2 exon
GTTTTTGTTTACAGATTACAATAGACTGTCCAGTGTAGGTGGAGAAACTTCTCTGGCTGAAATGATTGCAACCCTCTCGGATGCTTGTGAAAGAGAGTTTGGCTTTTTGGCAACCAGGCTTTTTCGAGTATTCAAGACTGAAGATACTCAGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000134313:ENST00000256707:15
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:
PF076939=KAP_NTPase=FE(10.7=100)
A:
NA
C2:
PF076939=KAP_NTPase=FE(11.0=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
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