HsaINT0090485 @ hg19
Intron Retention
Gene
ENSG00000135862 | LAMC1
Description
laminin, gamma 1 (formerly LAMB2) [Source:HGNC Symbol;Acc:6492]
Coordinates
chr1:183086669-183087281:+
Coord C1 exon
chr1:183086669-183086858
Coord A exon
chr1:183086859-183087168
Coord C2 exon
chr1:183087169-183087281
Length
310 bp
Sequences
Splice sites
5' ss Seq
CAGGTAAGA
5' ss Score
10.77
3' ss Seq
GGCCCTTTCTTTCTCTCCAGGCT
3' ss Score
10.97
Exon sequences
Seq C1 exon
CAAAGTTCTTGGGCAAGCAGGTGTTGAGTTATGGTCAGAACCTCTCCTTCTCCTTTCGAGTGGACAGGCGAGATACTCGCCTCTCTGCAGAAGACCTTGTGCTTGAGGGAGCTGGCTTAAGAGTATCTGTACCCTTGATCGCTCAGGGCAATTCCTATCCAAGTGAGACCACTGTGAAGTATGTCTTCAG
Seq A exon
GTAAGATAGCCTTCTTTGTAAAGTGAGACTTGACGAACATTGTGAAAGTGGTGTCTTTATTTAAGTTTAACTGGCCTCTAGATGTATTTTAAAGAAAAACTTCTGGGTTATTGTGGTGATTTTGTAAAAGGGAGCCTTCCTTTCTTTACCTTTATCTTTTCCAATTGTACTACCAAACCAATAGTCTTATTTTTTATTTGATTTGATTGTTAGAGCATTGCATTGTTGGGGCATAAATGAATAAGAAATATTTCCCCAACATCCAGAATTGTCCTTACAGAGGTTAATGTGGCCCTTTCTTTCTCTCCAG
Seq C2 exon
GCTCCATGAAGCAACAGATTACCCTTGGAGGCCTGCTCTTACCCCTTTTGAATTTCAGAAGCTCCTAAACAACTTGACCTCTATCAAGATACGTGGGACATACAGTGAGAGAA
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000135862-LAMC1:NM_002293:10
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:
PF0005213=Laminin_B=FE(48.1=100)
A:
NA
C2:
PF0005213=Laminin_B=FE(29.0=100)
Main Inclusion Isoform:
NA

Other Inclusion Isoforms:
NA
Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
CAAAGTTCTTGGGCAAGCAGG
R:
TCTCTCACTGTATGTCCCACGT
Band lengths:
302-612
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)