Special

HsaINT0097537 @ hg19

Intron Retention

Gene
Description
latent transforming growth factor beta binding protein 2 [Source:HGNC Symbol;Acc:6715]
Coordinates
chr14:74995186-74995825:-
Coord C1 exon
chr14:74995661-74995825
Coord A exon
chr14:74995402-74995660
Coord C2 exon
chr14:74995186-74995401
Length
259 bp
Sequences
Splice sites
5' ss Seq
CAGGTAACC
5' ss Score
8.66
3' ss Seq
TCTGGCTGTTGGCTTTGCAGAGG
3' ss Score
8.43
Exon sequences
Seq C1 exon
CGGACAAGGCAATCTCCATGCTGCAGGGACTGTGCTACCGGTCGCTGGGGCCCGGCACCTGCACCCTGCCTTTGGCCCAGCGGATCACCAAGCAGATATGCTGCTGCAGCCGCGTGGGCAAAGCATGGGGCAGCGAGTGTGAGAAATGCCCTCTGCCTGGCACAG
Seq A exon
GTAACCTCCTGTTCCCATCCCAGCTTTCACTGCCCAGGGGCTCAAGGCCAGTGACCATGTTGCCAGGCCTGGGTAGACTTCCCTCAATCTGGAAGACTGAAGTAGCCTTCCCTGCCTGCTCACGTGCTTATCCCAACCTGGGGCTCCCTCCCTCCTTGCTGCCACAATTGCCGTGTCTCCCAAAGGGAGGGAAAGGAAGGCCCTGGTTTCCTGCAGGAACAGCACCTCTCAGTTTGTCCTCTGGCTGTTGGCTTTGCAG
Seq C2 exon
AGGCCTTCAGAGAGATCTGCCCTGCCGGCCACGGCTACACCTACGCGAGCTCCGACATCCGCCTGTCCATGAGGAAAGCCGAGGAGGAGGAACTGGCAAGGCCCCCAAGGGAGCAAGGGCAGAGGAGCAGCGGGGCACTGCCCGGGCCAGCAGAGAGGCAGCCCCTCCGGGTCGTCACGGACACCTGGCTTGAGGCCGGGACCATCCCTGACAAGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000119681-LTBP2:NM_000428:11
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=0.671
Domain overlap (PFAM):

C1:
PF0068312=TB=PU(86.0=66.1)
A:
NA
C2:
PF0068312=TB=PD(11.6=6.8)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GGACAAGGCAATCTCCATGCT
R:
CTGCTCCTCTGCCCTTGCTC
Band lengths:
294-553
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