Special

HsaINT0031740 @ hg19

Intron Retention

Gene
ENSG00000171219 | CDC42BPG
Description
CDC42 binding protein kinase gamma (DMPK-like) [Source:HGNC Symbol;Acc:29829]
Coordinates
chr11:64606126-64606705:-
Coord C1 exon
chr11:64606505-64606705
Coord A exon
chr11:64606375-64606504
Coord C2 exon
chr11:64606126-64606374
Length
130 bp
Sequences
Splice sites
5' ss Seq
GAGGTCTGG
5' ss Score
2.59
3' ss Seq
CCCCCTCCCCCGACCCACAGGAC
3' ss Score
11.15
Exon sequences
Seq C1 exon
GTGGATTCATCAGTGGCAGTAGGGACGCCGGACTATATCTCCCCTGAGATCCTGCAGGCCATGGAGGAGGGCAAGGGCCACTACGGCCCACAGTGTGACTGGTGGTCGCTTGGAGTCTGCGCCTATGAGCTGCTCTTTGGGGAGACGCCCTTCTATGCTGAGTCCTTGGTGGAAACCTACGGCAAGATCATGAACCACGAG
Seq A exon
GTCTGGACACCAGGCTCTGGGCTTCCAGAGGGGGCAGTGGGACCCCTGAGTCTGTGTGGTTGGAAGTACCGGCAGGTGAGGCTGGGTTCCTGGACACTTGACCCAGCCTGCCCCCTCCCCCGACCCACAG
Seq C2 exon
GACCACCTGCAGTTCCCCCCGGACGTGCCTGACGTGCCAGCCAGCGCCCAAGACCTGATCCGCCAGCTGCTGTGTCGCCAGGAAGAGCGGCTAGGCCGTGGTGGGCTGGATGACTTCCGGAACCATCCTTTCTTCGAAGGCGTGGACTGGGAGCGGCTGGCGAGCAGCACGGCCCCCTATATTCCTGAGCTGCGGGGGCCCATGGACACCTCCAACTTTGATGTGGATGACGACACCCTCAACCATCCA
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000171219-CDC42BPG:NM_017525:7
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=0.349
Domain overlap (PFAM):

C1:
PF0006920=Pkinase=FE(24.7=100)
A:
NA
C2:
PF0006920=Pkinase=PD(16.5=53.0),PF0043319=Pkinase_C=PU(41.7=24.1)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
AGACGCCCTTCTATGCTGAGT
R:
TCAGGAATATAGGGGGCCGTG
Band lengths:
247-377
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