Special

HsaEX0026116 @ hg19

Exon Skipping

Gene
Description
formin binding protein 1 [Source:HGNC Symbol;Acc:17069]
Coordinates
chr9:132671169-132687436:-
Coord C1 exon
chr9:132687239-132687436
Coord A exon
chr9:132686123-132686305
Coord C2 exon
chr9:132671169-132671278
Length
183 bp
Sequences
Splice sites
3' ss Seq
GCTCCATCTCTTACATGTAGCTT
3' ss Score
5.85
5' ss Seq
GGGGTAAGT
5' ss Score
9.65
Exon sequences
Seq C1 exon
GATTCACAGCTGGTAATAGAAGCTTATAAATCAGGGTTTGAGCCTCCTGGAGACATTGAATTTGAGGATTACACTCAGCCAATGAAGCGCACTGTGTCAGATAACAGCCTTTCAAATTCCAGAGGAGAAGGCAAACCAGACCTCAAATTTGGTGGCAAATCCAAAGGAAAGTTATGGCCGTTCATCAAAAAAAATAAG
Seq A exon
CTTATGTCCCTTTTAACATCCCCCCATCAGCCTCCCCCTCCCCCTCCTGCCTCTGCCTCACCCTCTGCTGTTCCCAACGGCCCCCAGTCTCCCAAGCAGCAAAAGGAACCCCTCTCCCATCGCTTCAACGAGTTCATGACCTCCAAACCCAAAATCCACTGCTTCAGGAGCCTAAAGCGTGGG
Seq C2 exon
GGTGCAACACCGGAGGATTTCAGCAACCTCCCACCTGAACAAAGAAGGAAAAAGCTGCAGCAGAAAGTCGATGAGTTAAATAAAGAAATTCAGAAGGAGATGGATCAAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000187239_MULTIEX2-1/3=C1-C2
Average complexity
C1*
Mappability confidence:
100%=100=100%
Protein Impact

Alternative protein isoforms (Ref)

Show PDB structure
Features
Disorder rate (Iupred):
  C1=0.641 A=0.734 C2=0.979
Domain overlap (PFAM):

C1:
NO
A:
NO
C2:
PF039618=DUF342=FE(28.8=100),PF136541=AAA_32=FE(24.0=100),PF143891=Lzipper-MIP1=PU(34.9=78.4),PF0396210=Mnd1=PU(28.1=73.0),PF154561=Uds1=PU(37.8=91.9),PF0043516=Spectrin=PU(32.1=70.3),PF0218511=HR1=PU(31.5=62.2)


Main Inclusion Isoform:


Main Skipping Isoform:


Other Inclusion Isoforms:


Other Skipping Isoforms:
NA
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
ATCAGGGTTTGAGCCTCCTGG
R:
TCATCGACTTTCTGCTGCAGC
Band lengths:
243-426
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