Special

HsaEX0009265 @ hg38

Exon Skipping

Gene
Description
otogelin like [Source:HGNC Symbol;Acc:HGNC:26901]
Coordinates
chr12:80279028-80302783:+
Coord C1 exon
chr12:80279028-80279166
Coord A exon
chr12:80296827-80296961
Coord C2 exon
chr12:80302634-80302783
Length
135 bp
Sequences
Splice sites
3' ss Seq
AAATATTTGTGACATTTCAGAGT
3' ss Score
4.44
5' ss Seq
CAGGTTAGT
5' ss Score
8.02
Exon sequences
Seq C1 exon
CGTTTGTCGACGAGGAATGTTCAATTGCACATATTATCCATGCCCAGCAGTGTGCACAATATACGGGGACCGACATTATTATTCTTTTGATGGACTAGAATATGACTATATCAGTGATTGCCAGGTGTTTTTGATAAAG
Seq A exon
AGTGCAGATGATTCAGATATATCTGTCATTGCCCAGAACAAGAAATGCTTTGACAACGATATTGTTTGTTCTAAAAGTGTTTTGATTTCAGTTGGGGACACTGAAATTTACCTGAATGATACTCCTTACAAACAG
Seq C2 exon
AAACAATCAGGTTTTTTTCTGGAAAACAAATCTACCTACCAGCTTTGGAAGGCTGGTTACTATATAGTAGTATACTTTCCAGAGAAAGATATCACTATTCTTTGGGATAGGAAGACAACTATTCATATCAAAGTTGGGCCACAGTGGAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000165899_CASSETTE2
Average complexity
S
Mappability confidence:
100%=100=100%
Protein Impact

Alternative protein isoforms (Ref)

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

C1:
PF0009420=VWD=PU(18.9=59.6)
A:
PF0009420=VWD=FE(29.7=100)
C2:
PF0009420=VWD=FE(33.1=100)


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:
TTATCCATGCCCAGCAGTGTG
R:
CTTCCACTGTGGCCCAACTTT
Band lengths:
256-391
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