HsaINT0090249 @ hg19
Intron Retention
Gene
ENSG00000053747 | LAMA3
Description
laminin, alpha 3 [Source:HGNC Symbol;Acc:6483]
Coordinates
chr18:21353461-21355887:+
Coord C1 exon
chr18:21353461-21353551
Coord A exon
chr18:21353552-21355755
Coord C2 exon
chr18:21355756-21355887
Length
2204 bp
Sequences
Splice sites
5' ss Seq
TCCGTAAGT
5' ss Score
10.27
3' ss Seq
AAAACTGGGATTTCTCTTAGCCT
3' ss Score
2.29
Exon sequences
Seq C1 exon
CACAACACAGCTGGAGTAAACTGTGAACAGTGTGCTAAGGGCTATTACCGCCCTTATGGGGTTCCAGTGGATGCCCCTGATGGCTGCATCC
Seq A exon
GTAAGTTTCATTTCAAGTTGGTGTATCTTAGCCTGTGTGTACTGCCTCAGCGAAGTCATCAGGCTAACTTTGGATCAGTTAATAACTTCCTTCATGCCCTCTCTCTTCAGAGTATTAGTTGTGCTCGCTATGTGACCTCAGTCACTTACACAGTCTCTTTGAATTTTGGATTTATTGCATGTAAATGGAAATGATAATGTATTTCATAAGATTAAATAAAATGCAATCAAAAGCATGTAGGAAAATACTTACCATTGGGCCTGTCACATATTAGGCCTGTGATAAATGTTAGTTTCTCCATTTTCTGTTGTTTTGACATGTTTCTATGATCTCTAATAATTTCAATTTTTGGGCTGGAGGCAGTGGCTCAGGCCTGTAATCCCAGGACTTTGGGAGGCTGAGGCAGGTGGATCACTTGAGGCCAAGAGGTCAAGACAAGCCTGGTCAACATGGTGAAAAACCCTGTCTCTACTAAATAGAAAAAAATTAGCCAGGTGTGGTGGTGCTCACCCGTAATCCTAGTTACTCTGGAGGTGGAGGCATGAGAATTGCTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCCAAGATCACGCCACTGCACTCCAGCCTGGATGACAGAGTGAGACTCTGTCTCAGAAGCAACAACAACAACTTGAATTAGAACAAGACAACACAGTAATGAGTTCATAAGGATTTAATAATAGTCACATTGTTTAAAATAGCTAATATTTGTTGAGTACTTGCCATATATGAGGCATTACCTAAATACTTTCACAAAGGTCTTGTTTAATTATTACAACAAATAGGACATTGTATTATTGTCCTCATTTTTAGATACGGAGAAACCAAACAGTCTGAGTAGTTATATATAATTTAGGCTAGGTGACAAAACCGCTAACTGCTAGATCCAGGATATAGTTCTTTTCTGTCTGACATGACTGTGCCATAACTCTTCTATTATACAGAAGAATGCCTCTAGTTTTTCCTTGTAGAATTATGAATCTTGGGTCAGATTTACAGACTTTTCCCTACATGTGCAACCTATACCCTATTCAATGCTTGGTTCTTTTAAGTTGTCTGGTTGTCACAGTTGGAAAGCAATTCCAGTCCTGAAGTCAATCCTGTGCCCACTCCATGATTAATCATACCATTAACATTTGTGGGTATTAAAGTCCAGGGAATATGTAGATGGATTTACTTCTCTCTAGGGCATTCTTAGTTGTTAAAAAAAATGTGTTTTCACTTTTCTTCCTTCTTCCACATCATGCTGCAAAGTATGTCTATCACCTGTCTTGTGCCTACAAAGAATAGGCATTGGGAAAGGAAAACAGGACATTGCCAATGTAATTGTACCTCATTAGGAGCCTCACTGTTTCATCACCTTTCTAGTTTTTTCATCATTGAAGTGGTCCACAGAGGTATTAGAGGCTTGGCGTAAAGGATCAGTAGGACACATGAATCCTAACTAAATTAAGCAAAGGACACCAGGATGCCAGGTCACCCAGGTCTTTACAGGAGATGTATTCAGATGAGCTGTGACAGTATTTTCCCTGTCCAGGGTGCACCTGCCAGGTCAAGGGAGGCCCCCAAGTGGGAGGTCGACAATCTTCTTATACTTGCACTATGCCTTACTCCAGTGCAAGCCTGATAATCGTGCCCGATAATCGTTTTTGGTTGCAAAAGCTGCCTTCAGTAAGCCATTTCACTCAGATTAACATTTTTTTTATGGGTCTTGGTCTGCTGTCCACAGACTCTATCTCCATGTCTAGGCACTCCACACTTGCATCTGTATCATAACTGTGTATTGATGACCACTTTGTGGGCATTCACAGTTGGTTCATAGCTAGAAAGGGCTGTGCCCAACAGAACTAAGGCAAATACCCCCACCCCCACCCCCAACCCCTCTGACTGTAGCATGCAGGCTTTGCCTCTGACTCAGTGAGCTGGGCAATGCTCAGTGGGATAAATGACATCCATGAGAACTTCTGTGTGGACGCTCATTACAGCTGATCTCTGACAGCTCACGAGCTTCGGGCAGTGAGAACCATCAATCAGGTGTGAGGTGGGAAATAGGCTGTGCCCTTTCAAGAATACCTATAGACCAAGGATCAAGTATGGAACGTTGCCTGGGAAGTGTTGGAACATATTTGCTTTGTTAAGTGCAGTGAAGGACGGATCCTTTGAAAACTGGGATTTCTCTTAG
Seq C2 exon
CCTGCAGCTGTGACCCTGAGCATGCGGATGGCTGTGAACAGGGTTCAGGCCGCTGTCACTGCAAGCCAAATTTCCACGGAGACAACTGTGAGAAGTGTGCAATTGGATACTACAATTTCCCATTTTGCTTGA
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000053747-LAMA3:NM_001127717:9
Average complexity
IR-S
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:
PF0005319=Laminin_EGF=PD(41.2=90.3)
A:
NA
C2:
PF0005319=Laminin_EGF=WD(100=95.6)
Main Inclusion Isoform:
NA
Other Inclusion Isoforms:
NA
Other Skipping Isoforms:
Associated events
Other assemblies
Conservation
Zebrafish
(danRer10)
No conservation detected
Fruitfly
(dm6)
No conservation detected
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
Other AS DBs:
FasterDB (Includes CLIP-seq data)
AS-ALPS (AS-induced ALteration of Protein Structure, links to PINs)
APPRIS (Selection of principal isoform)
DEU primates (Only for human)