Special

HsaEX0035806 @ hg19

Exon Skipping

Gene
Description
LIM domain and actin binding 1 [Source:HGNC Symbol;Acc:24636]
Coordinates
chr12:50575687-50589670:-
Coord C1 exon
chr12:50589613-50589670
Coord A exon
chr12:50586235-50586344
Coord C2 exon
chr12:50575687-50575820
Length
110 bp
Sequences
Splice sites
3' ss Seq
TCCTTTTGTAACTCAAGCAGGTG
3' ss Score
4.98
5' ss Seq
AAGGTATGA
5' ss Score
9.11
Exon sequences
Seq C1 exon
ATTTCTGCAAATGAGAATAGCCTGGCAGTCCGTTCCACCCCTGCCGAAGATGACTCCC
Seq A exon
GTGACTCCCAGGTTAAGAGTGAGGTTCAACAGCCTGTCCATCCCAAGCCACTAAGTCCAGATTCCAGAGCCTCCAGTCTTTCTGAAAGTTCTCCTCCCAAAGCAATGAAG
Seq C2 exon
AAGTTTCAGGCACCTGCAAGAGAGACCTGCGTGGAATGTCAGAAGACAGTCTATCCAATGGAGCGTCTCTTGGCCAACCAGCAGGTGTTTCACATCAGCTGCTTCCGTTGCTCCTATTGCAACAACAAACTCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000050405_CASSETTE1
Average complexity
S*
Mappability confidence:
100%=100=100%
Protein Impact

ORF disruption upon sequence exclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.950 A=1.000 C2=0.044
Domain overlap (PFAM):

C1:
NO
A:
NO
C2:
PF0041217=LIM=PU(61.4=77.8)


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Skipping Isoforms:
NA
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
TGCAAATGAGAATAGCCTGGCA
R:
TGAGTTTGTTGTTGCAATAGGAGC
Band lengths:
186-296
Functional annotations
There are 1 annotated functions for this event
PMID: 17875928
Encodes an experimentally validated Eukaryotic Linear Motif (ELM). Method: classical fluorescence spectroscopy, detection by mass spectrometry, mutation analysis, protein kinase assay, western blot. ELM ID: ELMI001447; ELM sequence: KPLSPDA; Overlap: FULL


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains
  • Pre-implantation embryo development