Special

HsaINT1006186 @ hg38

Intron Retention

Gene
ENSG00000151062 | CACNA2D4
Description
calcium voltage-gated channel auxiliary subunit alpha2delta 4 [Source:HGNC Symbol;Acc:HGNC:20202]
Coordinates
chr12:1874604-1875337:-
Coord C1 exon
chr12:1875251-1875337
Coord A exon
chr12:1874676-1875250
Coord C2 exon
chr12:1874604-1874675
Length
575 bp
Sequences
Splice sites
5' ss Seq
TCTGTGAGT
5' ss Score
7
3' ss Seq
CATTGTCTTTCCTCCTGAAGCTG
3' ss Score
7.75
Exon sequences
Seq C1 exon
TACAGAGAGGGGAAGAAACTAAAACCCAAACCTAACTACAACAGTGTGGATCTCTCCGAAGTGGAGTGGGAAGACCAGGCTGAATCT
Seq A exon
GTGAGTGGGGAAAATAGGGGGAAGGGAAGCTAGTTAGGCTCTACATCCAACTAAATGGGTCAGCTGTGTGGCTGTGAGCTTTGAGGTCACTCTGTTCCTGTCAGGCAGAACAGGTTCATCCCAGAGCCTTTCCAAGCTCAAGCCACAAGCAATGCCTAAAATGAGCAATTCTTTTAACAACTATAAAAATATAACAATATCTTCTTGAATCACAAGGACTACTGAGGCTGGATGAGATCATGTGTATAAGCTGCAGAGTCTGAGTTTTAGTGATGTTTTAGCCTGGCTTTTGATTGCAATATCTCGTCCTAGAGGAAATTATGTCCCAGCAACTTGGCACTCTGTACCCCAATGCATCAGTGCACATGGGAGTGGGATCTTGGTGAATGCCTGGAATTATGAGCTAGATGGAGCTTAGAGTCAGGTCCATCTTCCCTCCTGGTATCTCTCTCAGAGGAAAAAGGGAAGAACCAAAAGTGTTTCTGGGGATCACCTCTAATCTGGTCTGAAGAATGCCATACTTTCACCATCCCCTGTGAGCCAAGGAACTAATGCCATTGTCTTTCCTCCTGAAG
Seq C2 exon
CTGAGAACAGCCATGATCAATAGGGAAACAGGTACTCTCTCGATGGATGTGAAGGTTCCGATGGATAAAGGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000151062:ENST00000382722:17
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.201 A=NA C2=0.065
Domain overlap (PFAM):

C1:
PF0274313=Cache_1=PD(6.4=20.7)
A:
NA
C2:
NO


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Primers PCR
Suggestions for RT-PCR validation
F:
No suggested primer sequences
R:
No suggested primer sequences
Band lengths:
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains