Special

HsaINT0090233 @ hg38

Intron Retention

Gene
Description
laminin subunit alpha 3 [Source:HGNC Symbol;Acc:HGNC:6483]
Coordinates
chr18:23842611-23845124:+
Coord C1 exon
chr18:23842611-23842750
Coord A exon
chr18:23842751-23845008
Coord C2 exon
chr18:23845009-23845124
Length
2258 bp
Sequences
Splice sites
5' ss Seq
TTGGTGCGT
5' ss Score
6.18
3' ss Seq
TGCTGGTGGATTTCTTTCAGGTC
3' ss Score
8.37
Exon sequences
Seq C1 exon
GCTCCTTCCATGCCTCTTTTTGCCCCCATGTGCTTGGCTGCCGGGATCAAGTGATTGCCGAAGGCCAGATTGAGTTTGACATCTCAGAGCCTGAAGTGGCCGCAACTGTGAAGGTTCCAGAAGGAAAGTCCTTGGTTTTG
Seq A exon
GTGCGTTCCACTCGTTCCTCAACTTGCTCCTCACATGCCTGCCTGGCTGGCCATTCTGGGTGTCTGTTTAGCTCATGGAAATAATTCTTCCAAGGAATTGAAGTCATATTTGTAGAAAAATGTTTAAATTTTACAGCTGTCTTTTACCCCCCAATAAATAAATAAATAAAGCATGTGACAATTAAAGTCAAGGGAACTAGGACAGAAGAGAGTAGGCGTCGCCCCTCTCCACCAGCCCCTGCTTCCTCATCTGACCAGTCTCTGGAGCATTTTTCGCTCCTTTCTTCTTTTGGCCCCTGCAGCTGCTTTCTCTCTGTTTTCCCTGCTTTCTCTAGCGCTCCTTGGGTGATTTCTCTTTTCCACTTGTCACTGTGTGTTGGCGTTCCTTCCGATTTGACACCGAGCCCCTCATTGTGTCATTTCTCCTTGGATACATCTTCCGTGCCCATCGATTCTATTCTCTCCACTGTGGGAAGGACACCCACATCTGTGAGGTCATCTCTGATCTTTCCTGAACTCCAGTATGTGACCACCATCTCCTGCGTATCTGCCTGGCCAGAGATCTTGAAAGTCCCTTGCTTAGTCTGCACCCTGCATAGCCCCGATGTGCCTACCCTTTTCATCACCTTGAGTGATGACAACCAGTGCCTGGAGTCATGCTGACCCCCCTTCTCTAGCAGCTCTGCTCCCACATCTGTTACCACACCCCAGAGTCTTTCTCTGCCGTGCCTCCTGGAGGCAACCATTCTCTTCTAGCCCCGTTGTCCTCACTGACCATCCTTCCTCTCACTTGGGCAGGGCCAGCCTCCTGGCAGCACTCCCTTCCTGTTCCACCTCCTTCCAGTGCCTCCTCCGCACTCCTGGCCATTACCTACCTGGCTGGAGGGATTAGAGCATGCCCTGTGACCCAGCCACTTCTCTGGGCTTCCAACAACTGATGGGATACACTCCATGTATTTCCCTAGGATCCACGTGCCTCACTCAGGCCCTCACGACCCCCTAATTCATCTTTTATCTTTCTCTCTGCCATTGCCCTACTCCACGCCTCCCACACCTCACGCTCTGGCCATACAAATCCGTTCTCAAACCCCCAGATATGCCATGTCCTCTCATGCCACCAGGCTTTCTCACACTGTCCCTTTTTCTGACATTTTCTGTCTGTTTCTCTACCTGGATAAGTCCAGCCTACCCACTCACCCAGCTCAGAGTTAATTTGTCTTTCTGCAAAGCCCTCCAGGAAGCATTGCCCAGACTCTCTGTGTGGCCCTCCAGGTCTCTGAGTGAGCCTCCTCCTCTCTGAGGAAGTCGTCTTCCCAGGAGACAAGGGCTGCATCTGTTCATTTTGCATCCCTTGTGCCTGGAATACCACCTGGTGTGTGGTGCTCAGCAAACGTTTATTGAATTGAATATCATGAGAGTAATAAGCTCCCTGTAAGCTGTGAGCTGGTGAGCAGTTGACAAAGATGTTTGAAAATTTCTACAGTGTTTGCTATAGGCATATTCTGATTTATACTGGCACAGAGAACCAAACTACCATTATTCATAATAGGGTACCAAGTATGATGAAAGCTCTAAGGACAAGCTAACACCTTCTTTCTGCATTGTTCTTGCCACTTTTGTTTGTTTCCCTTTAAAAATACAAAACAGCCATCCCTGGAGATCCAGGGAGACATCAGGCATGGGTCACATGGAGCCCTGGCCATCCAGCAGGCCCCTGCTTACCCTTAAGGTCCCGTGACCCAGCCAGCATGCAAGGCTTTTGCTTCTCTGAGTAGAAGTTCCAAGGGCTCTGCCTGGGAACTCATCATTCCCTGCACAGTAATGTGGACTGAGCCTTTACTCCTGGCTTTGGCCTGTTCCTGTGATTGTTTTTCATAAATCCTGATTCATTTGGTCTTGGTCTTAACAATAAGGGTGTTGATCTCAGTGAAGAGAAAGTACAGGTTGAAAATCTCTTATCTGAAATGATTGGGACCAGCAGTGTTTTGGATTTCAGATTTTTTTCAGATTTTGGAATATTTGCATAATACTTACAGATTGAGCATCCCTAATTCAAAAATCCCAAATCCAAAATGCTCCAGTGAGCATTTCTTTTGAGCATGATCTTTGAGCATCATGTCAGTGCTCAAAAAGTTTCAGATTTTGAAGCATTTCAGATTTTGGATTTTTCGAGTAGGGGTGCTCAACCTGTATAATAAGTAGCCTTAGGTCTGTGTCATCATTGGAAATTCTAAGACATGCTGGTGGATTTCTTTCAG
Seq C2 exon
GTCCGTGTTCTAGTGGTGCCTGCAGAAAACTATGACTACCAAATACTTCACAAAAAATCCATGGACAAGTCACTCGAGTTTATCACCAATTGTGGAAAAAACAGCTTTTACCTTGA
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000053747:ENST00000313654:29
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:
NO
A:
NA
C2:
NO


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