Special

HsaINT0097553 @ hg19

Intron Retention

Gene
Description
latent transforming growth factor beta binding protein 2 [Source:HGNC Symbol;Acc:6715]
Coordinates
chr14:74973401-74974013:-
Coord C1 exon
chr14:74973882-74974013
Coord A exon
chr14:74973527-74973881
Coord C2 exon
chr14:74973401-74973526
Length
355 bp
Sequences
Splice sites
5' ss Seq
TTGGTGAGT
5' ss Score
9.27
3' ss Seq
TGGTTCCCACTGTCCCACAGACA
3' ss Score
8.59
Exon sequences
Seq C1 exon
ATATTGACGAGTGTGAGGACTATGGAGACCCGGTGTGTGGCACCTGGAAGTGTGAAAACAGCCCTGGCTCCTACCGCTGTGTTCTGGGCTGCCAGCCTGGCTTCCACATGGCCCCGAACGGAGACTGCATTG
Seq A exon
GTGAGTAGGGAGGGAGGAGAGAGAGGAGAGAGGGCTGAGAAAACCTATTTTTCACATATTGAGCGAGACATGATTTTCTCCTGAGGACACGATTTTTTGCAGCTGATTGTAGCTTGTATATTTTCCATCCAGCAGAGCTTATGAAAGATGCCACAGGACTGTGAATGTTAGGATTTTCTTATCCTGGGTTGAGAGGCTGCTTTTCACAGGTCTTGGTGCTAATAAGCCAAATAAGTATTCTCAGCAGAGAACGAGAGAGTGTGCATGCGTGTGAGAGAGTGAGCACACACGCGCGCGCGCACACACACACACACACACACACACATCCTCTATCCTGGTTCCCACTGTCCCACAG
Seq C2 exon
ACATAGACGAGTGCGCCAACGACACCATGTGTGGCAGCCACGGCTTCTGTGACAACACTGATGGCTCCTTCCGCTGCCTCTGTGACCAGGGCTTCGAGATCTCTCCCTCAGGCTGGGACTGTGTGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000119681-LTBP2:NM_000428:26
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:
PF062476=Plasmod_Pvs28=FE(28.0=100),PF0764510=EGF_CA=WD(100=95.6)
A:
NA
C2:
PF0764510=EGF_CA=WD(100=95.3),PF0764510=EGF_CA=PU(0.1=0.0)


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:
TGACGAGTGTGAGGACTATGGA
R:
CCACACAGTCCCAGCCTGAG
Band lengths:
254-609
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