Special

HsaINT0090234 @ hg38

Intron Retention

Gene
Description
laminin subunit alpha 3 [Source:HGNC Symbol;Acc:HGNC:6483]
Coordinates
chr18:23747943-23749546:+
Coord C1 exon
chr18:23747943-23748060
Coord A exon
chr18:23748061-23749427
Coord C2 exon
chr18:23749428-23749546
Length
1367 bp
Sequences
Splice sites
5' ss Seq
CTCGTAAGT
5' ss Score
9.63
3' ss Seq
TTAAAATATTTTCCTTCTAGATT
3' ss Score
8.95
Exon sequences
Seq C1 exon
CTCTTCCATGTGGCCTATATTTTAATCAAATTTGCAAATTCTCCTCGCCCTGATCTTTGGGTCTTGGAAAGATCTGTAGACTTTGGAAGCACCTACTCACCATGGCAATATTTTGCTC
Seq A exon
GTAAGTAATCTTGCCTACCATGTTATGCATGGCTTTAATTACTTGGAACAGATAAAGACTATGGATTTAATTAGAAAATTAATCTTGGCTGGGTGTGGTGGCTCACCCCTATAATCCCAGCATTTTGGAAGGCCAAGGCGGGTGGATTACCTGAGGTCAGGAGTTTGAGACCAGCCTGGCCAACATGGTGAAACCCTGTCTCTACTAAAAATACAAAAATTAGCCAGGCACATGCCTGTTATCCCAGCTACTCGGGAGGCTGAGGTCGGATTATCACTTGAACCCAGGAAGCAGATGTTGCAGTGAGCCAAGATTGTACCACTGCACTCCAGCCTGGGCAACAGGATGAGACTCTGTCTCAAAAAAAAAAAAAAAAGAAAAGAAAATTAATCTCTCAGTATGACTAGTTAGGGACTGGTCACTTTTAACCTCTAAATTACTCTCAGAACATTGACTGGGCGCGGTGGCTTATGCCTGTAATCCCAGCACTTTGGGAAGCCAAGGCAGGCGGGTCACTTGAGGTCAGGAGTTTGAGACCAGCCTGGCTAACATGGTGAAACCCTGTCTCTACTAAAAATACAAAAATAAGCAAAGTGTGGTGGTGTGCACCTGTGGTCCCAGCTACTCGGGAGGCTGAGGTGGGAGAATCACTTGAATCCAGGAGGCGGAGGTTGCAATGAGCCAAGACTGTGCCACAGCACTCCAGCCTGGGTGACAGAGTGAGACTCCATCTTGGAAAAAAAAAAAAAAAGAATATCCCCATTTTTCAAGCATGTGTTCAATAATTTCAAGGATACTACATGCAGAAATGAAGTAGAAACTCCTTTTATGATAACAGTTCTTGGCACTATTTGGGAGTACCTGTAAGATGGTAGAAGCTGTGAATTGATGAGATGACTTTAATAACTGTCATCTCCAATCTTTTCCCCTTTATGCAGAATTAGAAACTAAGTTCCATCTTTATAGTTCCTGTGCTGTGCTTTACTTACCTCAACTCTGTTATCTTCACTAATGAAGAATGTCAGGGTTTCTGAACCCTATGATGAACAGAGGTGGACAAGAATTTTGCTTATAAAGGCATTGGGTTTTCCACTAGGTTTCCTTAGAAGATAAACTTGCCTAAGTATGAGCGTGGAGTTAGCACTGCATCTCCAAGCATTGCCACTGAAAGTCAACTGGCCTGAAATGGCTTGGTATTTTCTTTCATGAATTAAAAACTCCATTATCAGCCTTTCTCTAAAAGTTTTAAATGCCTTTCTGTTTTTTCTTTCTTTGTGTATTTTCTTAAGGAAACATAAGGCTTCTTAAGAGATTTGCAACAAAATGATAATATTTTGTTTTATAATATTAAAATATTTTCCTTCTAG
Seq C2 exon
ATTCTAAAGTAGACTGTTTAAAAGAATTTGGGCGGGAGGCAAATATGGCTGTCACCCGGGATGATGATGTACTTTGTGTTACTGAATATTCCCGTATTGTACCTTTGGAAAATGGTGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000053747:ENST00000313654:3
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

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

C1:
PF0005512=Laminin_N=FE(15.5=100)
A:
NA
C2:
PF0005512=Laminin_N=FE(15.5=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:
CTTCCATGTGGCCTATATTTTAATCA
R:
CCATTTTCCAAAGGTACAATACGGG
Band lengths:
231-1598
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