Special

HsaINT0026533 @ hg19

Intron Retention

Gene
ENSG00000151062 | CACNA2D4
Description
calcium channel, voltage-dependent, alpha 2/delta subunit 4 [Source:HGNC Symbol;Acc:20202]
Coordinates
chr12:1904465-1904946:-
Coord C1 exon
chr12:1904832-1904946
Coord A exon
chr12:1904546-1904831
Coord C2 exon
chr12:1904465-1904545
Length
286 bp
Sequences
Splice sites
5' ss Seq
TATATCCTG
5' ss Score
-28.05
3' ss Seq
TAACAGTGGCTTCTGCACATAAT
3' ss Score
-5.87
Exon sequences
Seq C1 exon
GGTATTTGTGGTGCAGCAGATTCCCAACAGTAACCTCCTCCTCCTGGTGACAGACCCCACCTGTGACTGCAGCATCTTCCCACCAGTGCTGCAGGAGGCGACAGAAGTCAAATAT
Seq A exon
ATCCTGCAATGCTCGGGGATGTGTGCGGTGGGGGCGGGGGCTGTAGGAGGTGTCTGTAGGGCTCAGATTTTGAGCAGCGGGGCCAGCCTCCTTCACCGCCCGTGTCCTCCACAGGGCTCCGTTATTTGTTCTCTAACCCTTCCCTGGGCCCCGGTGCTGCCTCCTGACCCTAAAGCTGCTTGCAGGGCAACTGGTGGCACCAGAGCAGGTTCTTCCAGACCTTTTTCCAGTCTGCAGAATGGGCTCCGGTCCTGAGATATTGACCTTAACAGTGGCTTCTGCACAT
Seq C2 exon
AATGCCTCTGTCAAATGTGACCGGATGCGCTCCCAGAAGCTCCGCCGGCGACCAGACTCCTGCCACGCCTTCCATCCAGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000151062-CACNA2D4:NM_172364:36
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

In the CDS, with uncertain impact

No structure available
Features
Disorder rate (Iupred):
  C1=0.000 A=NA C2=0.111
Domain overlap (PFAM):

C1:
NO
A:
NA
C2:
NO


Main Inclusion Isoform:
NA


Main Skipping Isoform:
NA


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Primers PCR
Suggestions for RT-PCR validation
F:
GGTATTTGTGGTGCAGCAGAT
R:
CTCTGGATGGAAGGCGTGG
Band lengths:
196-482
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Genotype-Tissue Expression Project (GTEx)
  • Autistic and control brains
  • Pre-implantation embryo development