Special

HsaALTA0003363-1/3 @ hg19

Alternative 3'ss

Gene
Description
formin homology 2 domain containing 1 [Source:HGNC Symbol;Acc:17905]
Coordinates
chr16:67265199-67265452:-
Coord C1 exon
chr16:67265333-67265452
Coord A exon
NA
Coord C2 exon
chr16:67265199-67265247
Length
0 bp
Sequences
Splice sites
5' ss Seq
CAGGTGAGT
5' ss Score
10.67
3' ss Seq
AAAGGGTCCTTTCAGAGCAGCGG
3' ss Score
-2.56
Exon sequences
Seq C1 exon
GAAATTGCTGAGCCACTGTTTGACCTGAAAGTGGGTATGGAACAGCTGGTACAGAATGCCACCTTCCGCTGCATCCTGGCTACCCTCCTAGCGGTGGGCAACTTCCTCAATGGCTCCCAG
Seq A exon
NA
Seq C2 exon
CGGCTTTGAGCTGAGCTACCTGGAGAAGGTGTCAGAGGTGAAGGACACG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000135723-24-27,24-26,24-25-1/3
Average complexity
Alt3
Mappability confidence:
NA
Protein Impact

ORF disruption when splice site is used (sequence exclusion)

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

C1:
PF0218118=FH2=FE(10.5=100)
A:
NA
C2:
PF0218118=FH2=FE(14.2=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GGTACAGAATGCCACCTTCCG
R:
CAGGTAGCTCAGCTCAAAGCC
Band lengths:
95-98
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