Special

HsaINT0003195 @ hg38

Intron Retention

Gene
Description
actinin alpha 2 [Source:HGNC Symbol;Acc:HGNC:164]
Coordinates
chr1:236737122-236739532:+
Coord C1 exon
chr1:236737122-236737214
Coord A exon
chr1:236737215-236739301
Coord C2 exon
chr1:236739302-236739532
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:ENST00000366578:9
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (disopred):
  C1=0.065 A=NA C2=0.045
Domain overlap (PFAM):

C1:
PF131021=Phage_int_SAM_5=FE(28.8=100),PF0043516=Spectrin=PU(9.9=35.5)
A:
NA
C2:
PF131021=Phage_int_SAM_5=PD(47.1=63.6),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