Special

HsaINT0031690 @ hg38

Intron Retention

Gene
ENSG00000198752 | CDC42BPB
Description
CDC42 binding protein kinase beta [Source:HGNC Symbol;Acc:HGNC:1738]
Coordinates
chr14:102946468-102947802:-
Coord C1 exon
chr14:102947721-102947802
Coord A exon
chr14:102946685-102947720
Coord C2 exon
chr14:102946468-102946684
Length
1036 bp
Sequences
Splice sites
5' ss Seq
AGGGTATGA
5' ss Score
6.84
3' ss Seq
TTCTGTTTCCTGTCATGAAGGTG
3' ss Score
6.13
Exon sequences
Seq C1 exon
AGATGACGAGTTTTCCGTGAGCTCAGTCCTGGCCTCAGATGTCATTCATGCTACACGCCGAGATATTCCATGTATATTCAGG
Seq A exon
GTATGAATTTTTCATTAATCTTTTTAACAAAGCACATGGTTAAAACTGATTGTTCTAGGCATGTCATTGTGCTGCGGCAGCCATCAGCGCACCTCCAGTGTGGCCCTAGGGTCTCAACCTCCAGCCTGGCTCCAGGTCCTTGTGCGTCCCGTCCTGGCCAAGTAGCAGCCTGTGCCCGTCTCGGGGAGCCTCCTGGCTGGCTTCTTCCCAGACACCCCTCTTCACTGACCCTCCCTTCTCCTACATCTGAAACTCCTCTTCCACTCAGTCCACGTCCCGGCCACTGTCCTCACAGCGTGTGCACTGCCAGGCGGGCGCTGTGGCAGGTTAGGCATGAAGGTGCCTCTCCAGTGCCCCCCAGCCAATTGGAGCCAGCGTTTTTGTTGACTGAGTGAGTGCTCCCTCACTGAGTTAGTGTTAGACATTGTAGCATTAGGACGTTCCTAGAAGACTGAATTGGGGAAAGAAACCCTCCAGCCCCCTCCACTGGGAATTTTCTTATAAACAGCAAAATTTTGATAACAAAACTAAGTCTATAAATTAGCTTTTACTAAATCACAGCTCTATTCAGAAACAACCCTGTCATACACAGTACAGGAAATTACCATCATTGTTACTGGAACGATGGTCATTTGGTAGCATGCGTGCTCAGAGGCTGCTCACAGGGAGGCATGATTTGGGCCAGTGTTTTTGAGATCTGCTTTTCCTGGACACATTTTCAGAATCTACTTTTATAATGATTATTCAAGAAAGCAGATTTAAAGTAGGCAGCTACTCGTAGTTTTGACAAAAGCAGAATTAACGAAAATGGGACCAGGAAGCGATCTCACGGGGCTGTTTAGAACCCCGCCCCTTCCGTGTCCTGCCGCGGGAGCCTCTGCAAGGCGCCCAGCGAGGTGGAGTCAGGGGTCCCTGCCTGGGAAGCACATCAGCCCCCGTTGCTCCTGGGGTGCGTGGCTCCAGCAGGGCCGTGGTAGCTGCGTGCGGCTTTGGCGTTTGATGACTTCTCTCTTCTCTTCTGTTTCCTGTCATGAAG
Seq C2 exon
GTGACGGCCTCTCTCTTAGGTGCACCTTCTAAGACCAGCTCGCTGCTCATTCTGACAGAAAATGAGAATGAAAAGAGGAAGTGGGTTGGGATTCTAGAAGGACTCCAGTCCATCCTTCATAAAAACCGGCTGAGGAATCAGGTCGTGCATGTTCCCTTGGAAGCCTACGACAGCTCGCTGCCTCTCATCAAGGCCATCCTGACAGCTGCCATCGTGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000198752:ENST00000361246:27
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:
PF0078017=CNH=PU(1.9=6.8)


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:
TGACGAGTTTTCCGTGAGCTC
R:
ACGATGGCAGCTGTCAGGAT
Band lengths:
294-1330
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