Special

HsaEX0012050 @ hg38

Exon Skipping

Gene
ENSG00000067191 | CACNB1
Description
calcium voltage-gated channel auxiliary subunit beta 1 [Source:HGNC Symbol;Acc:HGNC:1401]
Coordinates
chr17:39191474-39194970:-
Coord C1 exon
chr17:39194884-39194970
Coord A exon
chr17:39193449-39193797
Coord C2 exon
chr17:39191474-39191593
Length
349 bp
Sequences
Splice sites
3' ss Seq
CCTCATCCCTCCTGTTGCAGGAC
3' ss Score
10.59
5' ss Seq
GTGGTGAGC
5' ss Score
6.64
Exon sequences
Seq C1 exon
GGCAAATACAGCAAGAGGAAAGGGCGATTCAAACGGTCAGATGGGAGCACGTCCTCGGATACCACATCCAACAGCTTTGTCCGCCAG
Seq A exon
GACATGGCCAGGGCTGGGAAGAATGACGCTGTGCTTTTATTGCCCCTCTTGGCAGAAAAGGACCTTGGCTCCTTCAGTGTTTGCCAACCCAGGGAGTCAGACCCCAGCCTCCAATTCTTCCTCCTTTTAGCTCCCCAGCTCTGATCCCCGGTAGGTGGTGGGGAGTGGTGGAGGGGGGCAGTCCTTGCCACATCTCTGAGCTAAATATACCCTAGCAGTCTGCACATGTAGCAACTCTGCTTGTAACCCGAGCCCCCAAGGGAACGGGCAGTTTGGGCCACCCCCTAGGCCAGCAGGGCCAGGCACTGAGGGTGCCGGGATGGAGGCGCCCAGCCGGACCGTGGTGGTG
Seq C2 exon
GGCTCAGCGGAGTCCTACACCAGCCGTCCATCAGACTCTGATGTATCTCTGGAGGAGGACCGGGAAGCCTTAAGGAAGGAAGCAGAGCGCCAGGCATTAGCGCAGCTCGAGAAGGCCAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000067191_MULTIEX2-1/2=C1-C2
Average complexity
C1*
Mappability confidence:
100%=100=100%
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=1.000 A=0.085 C2=0.917
Domain overlap (PFAM):

C1:
NO
A:
NO
C2:
PF120523=VGCC_beta4Aa_N=PU(92.9=97.5)


Main Inclusion Isoform:
ENST00000394303fB1285


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
Conservation
Mouse
(mm9)
No conservation detected
Cow
(bosTau6)
No conservation detected
Chicken
(galGal4)
No conservation detected
Chicken
(galGal3)
No conservation detected
Zebrafish
(danRer10)
No conservation detected
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
GCAAATACAGCAAGAGGAAAGGG
R:
CTTGGCCTTCTCGAGCTGC
Band lengths:
206-555
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • The Cancer Genome Atlas (TCGA)
  • Genotype-Tissue Expression Project (GTEx)
  • Autistic and control brains
  • Pre-implantation embryo development