Special

HsaINT0008024 @ hg19

Intron Retention

Gene
ENSG00000130812 | ANGPTL6
Description
angiopoietin-like 6 [Source:HGNC Symbol;Acc:23140]
Coordinates
chr19:10204025-10204556:-
Coord C1 exon
chr19:10204369-10204556
Coord A exon
chr19:10204296-10204368
Coord C2 exon
chr19:10204025-10204295
Length
73 bp
Sequences
Splice sites
5' ss Seq
AAGGTGGGC
5' ss Score
7.93
3' ss Seq
TGACTTTCCTGCCCTGCCAGGCG
3' ss Score
8.46
Exon sequences
Seq C1 exon
GCCCGTGGCAGGATTGTGCAGAGGCCCGCCAGGCAGGCCATGAACAGAGTGGAGTGTATGAACTGCGAGTGGGCCGTCACGTAGTGTCAGTATGGTGTGAGCAGCAACTGGAGGGTGGAGGCTGGACTGTGATCCAGCGGAGGCAAGATGGTTCAGTCAACTTCTTCACTACCTGGCAGCACTATAAG
Seq A exon
GTGGGCACAGGTGGGCAGAGGCAGGGAAGGGGAGGGAGCCTGTTCTGGCTTCCTGACTTTCCTGCCCTGCCAG
Seq C2 exon
GCGGGCTTTGGGCGGCCAGACGGAGAATACTGGCTGGGCCTTGAACCCGTGTATCAGCTGACCAGCCGTGGGGACCATGAGCTGCTGGTTCTCCTGGAGGACTGGGGGGGCCGTGGAGCACGTGCCCACTATGATGGCTTCTCCCTGGAACCCGAGAGCGACCACTACCGCCTGCGGCTTGGCCAGTACCATGGTGATGCTGGAGACTCTCTTTCCTGGCACAATGACAAGCCCTTCAGCACCGTGGATAGGGACCGAGACTCCTATTCTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000130812-ANGPTL6:NM_031917:4
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.190 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF0014713=Fibrinogen_C=PU(28.6=96.8)
A:
NA
C2:
PF0014713=Fibrinogen_C=FE(42.3=100)


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:
TCTTCACTACCTGGCAGCACT
R:
GAAGCCATCATAGTGGGCACG
Band lengths:
167-240
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Genotype-Tissue Expression Project (GTEx)
  • Autistic and control brains
  • Pre-implantation embryo development