Special

HsaEX6044339 @ hg38

Exon Skipping

Gene
Description
formin homology 2 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:17905]
Coordinates
chr16:67238380-67239454:-
Coord C1 exon
chr16:67239348-67239454
Coord A exon
chr16:67238903-67238967
Coord C2 exon
chr16:67238380-67238447
Length
65 bp
Sequences
Splice sites
3' ss Seq
ACAGAGATCCTTGATTCCAGCAA
3' ss Score
0.75
5' ss Seq
TGGGTGAGT
5' ss Score
8.73
Exon sequences
Seq C1 exon
TTGGAGGATTGTGCTCTGCAAGTGTCTCCCTCCGGATACTACCTGGACACCGAGCTGTCCCTGGAAGAGCAGCGGGAGATGCTGGAGGGCTTCTATGAAGAGATCAG
Seq A exon
CAAAGGGCGGAAGCCCACGCTGATCCTTCGGACCCAGCTCTCTGTGAGGGTCAACGCTATCTTGG
Seq C2 exon
AAAAGCTGTATAGCTCCAGTGGTCCTGAGCTCCGCCGCTCCCTCTTCTCACTGAAGCAGATCTTCCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000135723-'6-10,'6-7,7-10
Average complexity
S
Mappability confidence:
100%=100=100%
Protein Impact

ORF disruption upon sequence exclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.009 A=0.000 C2=0.000
Domain overlap (PFAM):

C1:
NO
A:
NO
C2:
NO


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Inclusion Isoforms:


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
GGAGGATTGTGCTCTGCAAGT
R:
TTCAGTGAGAAGAGGGAGCGG
Band lengths:
160-225
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains