Special

HsaINT0026576 @ hg19

Intron Retention

Gene
ENSG00000167535 | CACNB3
Description
calcium channel, voltage-dependent, beta 3 subunit [Source:HGNC Symbol;Acc:1403]
Coordinates
chr12:49220150-49220637:+
Coord C1 exon
chr12:49220150-49220301
Coord A exon
chr12:49220302-49220541
Coord C2 exon
chr12:49220542-49220637
Length
240 bp
Sequences
Splice sites
5' ss Seq
AAGGTAAGT
5' ss Score
11
3' ss Seq
GCTCTGCCCTCCCCGCTCAGGTA
3' ss Score
9.45
Exon sequences
Seq C1 exon
CGGAAGTGCAGAGTGAGATCGAGCGCATATTTGAGCTGGCCAAATCCCTGCAGCTAGTAGTGTTGGACGCTGACACCATCAACCACCCAGCACAGCTGGCCAAGACCTCGCTGGCCCCCATCATCGTCTTTGTCAAAGTGTCCTCACCAAAG
Seq A exon
GTAAGTCAGCTGGGCTCATGGAGGAGGCCCACAGGGCTATCCTACTAGAATGTGGCATGATTCTACTTGGTCCCTGCCTGGGGCACCTGAGTTCCCTTTTCCTGCTGCCCTTAACACAACTCTGAGTCATCCTCACCTGCTACTGATGCCACAAGTGGAAGAAATGCCTAGCTCTGCCCGGGCTCAGCTCTGCCCAGAGTCCTGAGAGACTCCAGGCCTAGCTCTGCCCTCCCCGCTCAG
Seq C2 exon
GTACTCCAGCGTCTCATTCGCTCCCGGGGGAAGTCACAGATGAAGCACCTGACCGTACAGATGATGGCATATGATAAGCTGGTTCAGTGCCCACCG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000167535-CACNB3:NM_000725:10
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

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

C1:
PF0062516=Guanylate_kin=FE(27.6=100)
A:
NA
C2:
PF0062516=Guanylate_kin=FE(17.1=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
CGGAAGTGCAGAGTGAGATCG
R:
GTGGGCACTGAACCAGCTTAT
Band lengths:
246-486
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