Special

HsaEX0019769 @ hg38

Exon Skipping

Gene
Description
disco interacting protein 2 homolog C [Source:HGNC Symbol;Acc:HGNC:29150]
Coordinates
chr10:472439-486530:-
Coord C1 exon
chr10:486459-486530
Coord A exon
chr10:484781-484948
Coord C2 exon
chr10:472439-472549
Length
168 bp
Sequences
Splice sites
3' ss Seq
TTTTTTTCAACTTGTTACAGCAG
3' ss Score
7.01
5' ss Seq
TCGGTGAGC
5' ss Score
9.1
Exon sequences
Seq C1 exon
GTGACATCACACAAAAAGGATATGAAAAGAAGAGGTCAAAGTTAATTGGAGCCTACCTTCCGCAGCCTCCGA
Seq A exon
CAGCGAATGGAGCTGCCGTGGTTCGGTGTAGACTGCAGCACAGTGAAGGAGCGCCGAGGAGAACATTCCGCTCTGCCCACATCGGGGTGTGCGACGTCCGAGAAGCTGCGGCTCGGGAGCGGGTGGCCAGCACCGCAGGGAACCGGCCTCTGTTTTACTTTCGTTTCG
Seq C2 exon
GGGTGGACCAAGCTTTGCCGCAAGAACGCCGGGCTCCTGTCACTCCTTCCTCCGCCTCTCGCTACCACCGCCGACGGTCTTCAGGGTCACGAGATGAGCGCTATCGGTCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000151240_MULTIEX2-5/14=4-8
Average complexity
S*
Mappability confidence:
100%=100=100%
Protein Impact

Alternative protein isoforms (No Ref)

Show structural model
Features
Disorder rate (Iupred):
  C1=0.358 A=0.208 C2=0.866
Domain overlap (PFAM):

C1:
PF051207=GvpG=PD(42.2=76.0),PF064646=DMAP_binding=FE(25.3=100)
A:
PF064646=DMAP_binding=PD(50.5=84.2),PF064646=DMAP_binding=PU(8.1=10.5)
C2:
PF064646=DMAP_binding=FE(32.5=100)


Main Inclusion Isoform:


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GTGACATCACACAAAAAGGATATGA
R:
CGATAGCGCTCATCTCGTGAC
Band lengths:
178-346
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • The Cancer Genome Atlas (TCGA)
  • Genotype-Tissue Expression Project (GTEx)
  • Autistic and control brains
  • Pre-implantation embryo development