Special

HsaINT0003195 @ hg19

Intron Retention

Gene
Description
actinin, alpha 2 [Source:HGNC Symbol;Acc:164]
Coordinates
chr1:236900422-236902832:+
Coord C1 exon
chr1:236900422-236900514
Coord A exon
chr1:236900515-236902601
Coord C2 exon
chr1:236902602-236902832
Length
2087 bp
Sequences
Splice sites
5' ss Seq
GAGGTAAAG
5' ss Score
8.27
3' ss Seq
TTTTTGTGTTTGCGGAGCAGCTT
3' ss Score
3.36
Exon sequences
Seq C1 exon
GCCGAGACAGCGGCTAACAGGATATGTAAGGTTCTTGCTGTGAATCAAGAGAATGAGAGGCTGATGGAAGAATATGAGAGGCTAGCGAGTGAG
Seq A exon
GTAAAGGAAACTGGTGACCTGCAGTTCTGTCCATCCTCACGCAGGGGCTGAGGCACAGAGGGTGAAAAAATACTCCGTGGGGGCATATATATATATATATATATTTTGCATTTTTCATCTCAGATAGGATGAAAGTAGGAAAATACACTTGATCTCTGAGGTTGTTCCTATTGTAGTAACCTAACTTTTGGCAAAAACATAATCCCCAGTGGTCTTTCCAACGATCCCAAAGCAGAAAGGTATAGTTTGCATGTCTGAAGATAGGAGAATGCGATTCTCTGCTCAGCTCTGCACCTCCAGGGTTGGACACCCCTAGACGACCTTGGGTTACTTGTTTTTTTTTTTTCCTGTTCACTGGCTACCAACATCACATAGGATGCACTCCATATGCAAAAGCCTCACTCCACATAGGGACCCAGTGTCAAAGGAACTGGCCCAGCCTGGTGTGCGGAGCTGGCTCGGGCTCGTGTGTCTGTATAAATACCCAGAGGAAATCTGGGGAAGACAGAGCCCTCCCTGCAGAATATTTGAGCATGAGTTTCTGTGGTGCCTTTCCAGAGCTCTTCAGCTAGACTCTTGGTTAGGACAGCAGTTTCCAGGTTGTTTTTCTTTTCGTTCTTGTTATAGCATACGTAGCGACTACGCAGTATCCTCGCTGCATCTGCACTGTTTTCCCAAATACAAGCATGGGCTGCATGAGGCCCCCAGCCACCTCCTCTCTAAATTGGACTCAAGTACAGTGACACATACTTCAGACCAAATAATTTTTGCCAAGCCTTATTTTTTGCTTTGTTTTGTTTTGTTTTGTTTTCTATGACAGAGTCTTGCTCTCTGGCCCAGGCTGGAGTGCAGTGGGGCAGTCCTGGCGCACTGCAACCTCCGCCCCCAGGGTTCAAGCAATTGTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCGTGCACCACCACACCCAGCTAATTTTGTATTTTTAGTAGAGATGGAGTTTCACCGTGGTAGCCTGGCTGGCCTTGAACTCCTGACCTCAGGTGATCCACCCGCCTTGGCCTCCCAAAGTGCCGGGATTATTGGCGTGAGCCACCGCACCTGGCCTTCTTTTTAATTTAGCTGATATTTGGTCTTTATTGGGAAAAGTATCAGGACATTTGGAATAAATGTTCCAATAAATAGTAGTGTAACTTTATGATACTGAGTTCATATCTTCATACTGCTGCTATAGAAAAATTAAGCTTGATGGCATTGTTGAATGGCAGTGACAGGGTTGCCAGACATGAAGCATGGCCAGTACTGAAGGCCAGAGGATCCTTAGGAATTCAATTCTTCCTTTTCTTACTGGGTCCTTCATTTATCCTCCTAAAACCCTTAGACTCTAGGTATATCACCATTTAAACTATTTTTCATTCGAATCTGCTGTCATTTTCCAAGTGCTCAGTAGGCATAAGTGTAAATGATGGGGTTTTCAGCAAGTCATTTCTAAGACCTAGGTAGTAATTCAAGAGGTGCATGTGTATTTTGTCCTTAGGGATTCACTACCACGTTCGCTTTTATCATGCAGATTTACTTAAAAGCTAGACGTCAAAATACACTTTGGCATTGAGTTAGGCCCAGGCTTACAATACAGTTGTGTAGTAAGTAATCTAATTAGATTTGAGCTTATTTTTTAAAAACACATTTTAAGTGAAATCCAGTTCTTTGCTGAATTTATTACACTACAGTTCTGCCATGTCAAGTATTTTGGGGTTGTTTTGTTTTGTTTTTTGTTTTTTTAATTTGAAAGCTCCATCCAGCATTTGTCTGCTAATGTCTGGTCCCTGAGTTTCTTGTAAACGTCACATTTTTGTAAGACACGACTTTACGTGCTCACTTTAAGTTTTCGACCTGTGTTTGGTATCGTTGGGGTGATCACTCGCGGCCATGGGCGGACACTGAACATCTCGTTCATGCCTCTGTGCGTAGAGGTACCACATCTCAGTGATTTTAGGAACATTCATCCTTTACAAATTATTGGATGCCTCATTTTTTTTTTTTAACTGGGGGAGGGGGCTTGCTGGTGTCTTCAGCAGTATTTTTGTGTTTGCGGAGCAG
Seq C2 exon
CTTTTGGAATGGATTCGTCGCACGATCCCCTGGCTGGAGAACCGGACTCCCGAGAAGACCATGCAAGCCATGCAGAAGAAGCTGGAGGACTTCCGGGATTACCGCCGGAAGCACAAGCCACCCAAGGTGCAGGAGAAATGCCAGCTGGAGATCAACTTCAACACGCTGCAGACCAAGCTGCGGATCAGCAACCGTCCTGCCTTCATGCCCTCCGAGGGCAAGATGGTGTCG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000077522-ACTN2:NM_001103:9
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (disopred):
  C1=0.129 A=NA C2=0.019
Domain overlap (PFAM):

C1:
PF0043516=Spectrin=PU(9.9=35.5)
A:
NA
C2:
PF0043516=Spectrin=FE(68.5=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
Conservation
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
  • Pre-implantation embryo development