Special

HsaEX0044720 @ hg19

Exon Skipping

Gene
ENSG00000185585 | OLFML2A
Description
olfactomedin-like 2A [Source:HGNC Symbol;Acc:27270]
Coordinates
chr9:127557303-127563942:+
Coord C1 exon
chr9:127557303-127557410
Coord A exon
chr9:127561564-127561770
Coord C2 exon
chr9:127563693-127563942
Length
207 bp
Sequences
Splice sites
3' ss Seq
CAATCCTGCCCCCTCCGCAGAGC
3' ss Score
8.8
5' ss Seq
CAGGTGAGG
5' ss Score
10.07
Exon sequences
Seq C1 exon
CTGCAGTCCATGGTGGATCTCCTGGAGGGCACCCTGTACAGCATGGACTTGATGAAGGTGCACGCCTACGTCCACAAGGTGGCCTCCCAGATGAACACACTGGAAGAG
Seq A exon
AGCATCAAGGCCAACCTGAGCCGGGAGAATGAGGTGGTGAAGGACAGCGTGCGCCACCTCAGTGAGCAGTTGAGGCACTATGAGAATCACTCTGCCATCATGCTGGGCATCAAGAAGGAGCTGTCCCGCCTGGGCCTCCAGCTGCTGCAGAAGGATGCCGCCGCCGCCCCTGCCACCCCTGCCACGGGCACTGGTAGCAAGGCCCAG
Seq C2 exon
GACACAGCTAGAGGAAAAGGCAAGGACATCAGCAAGTATGGCAGTGTGCAGAAAAGCTTTGCAGACAGAGGCCTCCCAAAACCTCCCAAGGAGAAGCTGCTTCAGGTGGAGAAGCTGAGAAAGGAGAGCGGCAAGGGCAGTTTCCTCCAGCCCACAGCCAAGCCCCGCGCCCTGGCCCAGCAGCAGGCTGTGATCCGGGGCTTCACCTACTACAAGGCAGGCAAGCAGGAGGTGACCGAGGCGGTGGCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000185585_MULTIEX1-3/3=2-C2
Average complexity
S
Mappability confidence:
100%=100=100%
Protein Impact

Alternative protein isoforms (Ref)

No structure available
Features
Disorder rate (Iupred):
  C1=0.056 A=0.428 C2=0.760
Domain overlap (PFAM):

C1:
PF123083=Noelin-1=FE(33.0=100)
A:
PF123083=Noelin-1=PD(17.0=26.1)
C2:
PF118553=DUF3375=PD(10.3=11.9)


Main Inclusion Isoform:


Main Skipping Isoform:


Other Inclusion Isoforms:


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Zebrafish
(danRer10)
HIGH PSI
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
TGGACTTGATGAAGGTGCACG
R:
TGCTTGCCTGCCTTGTAGTAG
Band lengths:
292-499
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