Special

HsaINT0097620 @ hg19

Intron Retention

Gene
Description
latent transforming growth factor beta binding protein 4 [Source:HGNC Symbol;Acc:6717]
Coordinates
chr19:41129509-41129987:+
Coord C1 exon
chr19:41129509-41129637
Coord A exon
chr19:41129638-41129840
Coord C2 exon
chr19:41129841-41129987
Length
203 bp
Sequences
Splice sites
5' ss Seq
TCGGTACAA
5' ss Score
2.47
3' ss Seq
CTTAATCATCCTCTCCCTAGACA
3' ss Score
8.7
Exon sequences
Seq C1 exon
ACGTGGACGAATGTCAGCTCTTCCGAGACCAGGTGTGCAAGAGTGGCGTGTGTGTGAACACGGCCCCGGGCTACTCATGCTATTGCAGCAACGGCTACTACTACCACACACAGCGGCTGGAGTGCATCG
Seq A exon
GTACAAGCCCCACCTCCCCCAACCCCCGGCAACTCTCTCCAACCCCTAGCCTTGCCAGCTCCCCTCTGGAATGTGGCCACCACCAGCGGGAAGTCTTTCCTGGAGTCTAGACTCCATCCATCACACTGCCAATGTGCTGGGAAGAGAAATGGGAAAGGGTGGGGAGAGTTGAAGGGGATGCCTCTTAATCATCCTCTCCCTAG
Seq C2 exon
ACAATGACGAGTGCGCCGATGAGGAACCGGCCTGTGAGGGCGGCCGCTGTGTCAACACTGTGGGCTCTTATCACTGTACCTGCGAGCCCCCACTGGTGCTGGATGGCTCGCAGCGCCGCTGCGTCTCCAACGAGAGCCAGAGCCTCG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000090006-LTBP4:NM_003573:28
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:
PF0764510=EGF_CA=WD(100=95.5),PF0764510=EGF_CA=PU(0.1=0.0)
A:
NA
C2:
PF0764510=EGF_CA=WD(100=82.0)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GACGAATGTCAGCTCTTCCGA
R:
GGCTCTGGCTCTCGTTGGAG
Band lengths:
268-471
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