Special

HsaINT0090509 @ hg19

Intron Retention

Gene
Description
laminin, gamma 1 (formerly LAMB2) [Source:HGNC Symbol;Acc:6492]
Coordinates
chr1:183085902-183086577:+
Coord C1 exon
chr1:183085902-183086038
Coord A exon
chr1:183086039-183086454
Coord C2 exon
chr1:183086455-183086577
Length
416 bp
Sequences
Splice sites
5' ss Seq
TTGGTAATT
5' ss Score
5.73
3' ss Seq
TTTTCCTTCTCTACCTGCAGATG
3' ss Score
13.74
Exon sequences
Seq C1 exon
ATGCAAACCTGGATTTTTTAATCTGGAATCATCTAATCCTCGGGGTTGCACACCCTGCTTCTGCTTTGGGCATTCTTCTGTCTGTACAAACGCTGTTGGCTACAGTGTTTATTCTATCTCCTCTACCTTTCAGATTG
Seq A exon
GTAATTTAGACCTCATCCCCCAACCTGTTAGAACTGTGAGATTACACTTAAAATATTTTTAAAAATAAAATCAGTGACTCTTTGAGGGCTTTTTGATGGTTGGCAACACTTTGTATTATTTAGCATGCATAGTTTTTGTAGTTTGGCCTTTTAATTTAATGAAAATGTACTTTTGGCTTTAGAATTTATCTCAATGAATGGTGATTACAAATGTTATATAAATAGTAATAAAGTAAAATATAGTTTGAGTGGTATAGCATATATTGGTACTGTTGTAGGATCCATTTATTCAAAAAGGTTTATTGATGCCTTTCTGTATACAAGGTGTGGTCTTACACATTTTTATGATACATAGAGGACCTGAATTCAGGATGTTTACAGTGTAAAGTGCTTGTGTTTTCCTTCTCTACCTGCAG
Seq C2 exon
ATGAGGATGGGTGGCGTGCGGAACAGAGAGATGGCTCTGAAGCATCTCTCGAGTGGTCCTCTGAGAGGCAAGATATCGCCGTGATCTCAGACAGCTACTTTCCTCGGTACTTCATTGCTCCTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000135862-LAMC1:NM_002293:8
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(33.3=34.0)
A:
NA
C2:
PF0005213=Laminin_B=PU(3.8=11.9)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
CTGGAATCATCTAATCCTCGGGG
R:
CAGGAGCAATGAAGTACCGAGG
Band lengths:
238-654
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