Special

HsaINT0026589 @ hg38

Intron Retention

Gene
ENSG00000182389 | CACNB4
Description
calcium voltage-gated channel auxiliary subunit beta 4 [Source:HGNC Symbol;Acc:HGNC:1404]
Coordinates
chr2:151853448-151855375:-
Coord C1 exon
chr2:151855224-151855375
Coord A exon
chr2:151853544-151855223
Coord C2 exon
chr2:151853448-151853543
Length
1680 bp
Sequences
Splice sites
5' ss Seq
AAGGTAATT
5' ss Score
8.83
3' ss Seq
TTCATGTCTTCTTCTATCAGGTT
3' ss Score
10.04
Exon sequences
Seq C1 exon
CGGAAGTACAAAGTGAAATTGAAAGAATCTTTGAGTTGGCAAGATCTTTGCAACTGGTTGTTCTTGATGCAGACACCATCAATCACCCAGCACAACTTATAAAGACTTCCTTAGCACCAATTATTGTTCATGTAAAAGTCTCATCTCCAAAG
Seq A exon
GTAATTAGCTCCTTTCTGCCTTAAGGTTTAGAAGTGCATCTTTTAAAAATGTGTTTTGCTCTGTGGTTTTTTGTTAGTGGACAAAGGAGAACGTCTTGCTGATTATTAATAAGCACATTTAAAATCTTTCCACAGTGTACAGATTCTATGAATTTTCAGATAGTGAAGAATATAATAGTTCATTTCTTCTAAAAGCTACTATTGTAGATCCCAAACAAGACAGTTATGCAAGTGTATAATAGAAACAAAACATTAAGACAGATGTGGAAAAGTAGACTCTGGCTTATCATAGACTATGAATTCTATATTGGTAAATTTCTTGGATCCTGTTGATTCCTGTGTCATCCATACTCTGTACCTAGTTGAGAGAGTACATCTATATTGATCAAAAAAGGCATCTATGTTGATCATATATAAAATAGAATATCACTGTTTAAACATCTCCTATGGAAGCATTATAGACCCTGACATTTGTGCTTAGGTTGAGTTCTTGAAAGAATGTGGTTATTCCACGATAAGCACAATGGGAAATTTGCTTTGTATCTTTATGCCATTGTGGGAGGTAAAAATAAAAGTGAAATAGCCCCAAATTGGTTTCTTTTGATTTGGGTGTTCTTTCATTTTTAAAAAAGGATGTTGTTCTTAAAAAGTTAACGTGAAATGGTTACCCTTGGGAAGTACTATCTTAATAATCAGTTTCTTCTCTGTGCCTCCTAGTGTATTTTGGTGCCTAAATACAAATTCAACTGCCAACCAGCATGGCAGTCTTCTCTCATGGGTGGAGAATGTCTAAAGAAGCTGTACTCTCCTCCAGATGTTCTGAGATCCTAGCCTTCCATCTATCTCTGCAGACACTGCTTTGGTGCAGTGGACTTGGGAATCCTGAACAAACTAGGGCCTTTTGAGAATCAGTAGAATGGATTGAAAGAGCTGCTGGGGGTTCAAGCACTTCACTGCAGTGCAGGAGAGTTCAGCCCTTCCCACTGCCCATGACACTGTGGTGTCCTTAAGTGCAAGAACAGGAGTTCCCAGACACCTATGTCCTGGGGTATTATAGAGCTCATAGATTAGCATTGTTTGCAGGGGAAGGGCCACGGGACATGGCAGTATATGACCAAATGCAGTTACAGCAGTGGCCAAAAGACATAGATATATCACTGGTTTACATGTAGCAATATACTAATACAAATGTTTTGCCTGGGTCTCCAATCACAGAATAGTCTGATTAATTTAAAATTAAACTGAAATGTCCCATTAATAATCGGTGACAAAAATAACCAGAAAATGACTCTGACATTTATCTGACATGGAGATAGTGAGCTAAAACATTATTCAGGTGAATAATATTAAAGTATTACTTAACATAAATGACCTGGTACAGTCCACTCCCTCCATTTTTACAGGTCTCTCTTTGAAATCTCTGGGAAAAATCTAGGATGGGAACTCAGGCTCCTCCTGAGACTTCACACAGAGTTAGAATAGGATGAACATATCAAATCCATGGAACTGAGAGCCAATGTAAGCAGATGACATCATTACAGGTTTAAATATATGATTTCTCACACTGCATTTCCTCTCTGATAATACTCAGGGCCAAGCAGACCATTAAAAAGATCCTGGCTTATTTGATTTTCTTTCAACTCATCTACAATACCTCAGGTTCATGTCTTCTTCTATCAG
Seq C2 exon
GTTTTACAGCGGTTGATTAAATCTAGAGGAAAGTCACAAAGTAAACACTTGAATGTTCAACTGGTGGCAGCTGATAAACTTGCACAATGCCCCCCA
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000182389:ENST00000539935:11
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.006 A=NA C2=0.131
Domain overlap (PFAM):

C1:
PF0062516=Guanylate_kin=FE(24.6=100)
A:
NA
C2:
PF0062516=Guanylate_kin=FE(15.3=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:
CGGAAGTACAAAGTGAAATTGAAAGA
R:
TGTGCAAGTTTATCAGCTGCCA
Band lengths:
238-1918
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