HsaINT0082858 @ hg19
Intron Retention
Gene
ENSG00000056345 | ITGB3
Description
NA
Coordinates
chr17:45368320-45369934:+
Coord C1 exon
chr17:45368320-45368454
Coord A exon
chr17:45368455-45369504
Coord C2 exon
chr17:45369505-45369934
Length
1050 bp
Sequences
Splice sites
5' ss Seq
ACGGTGAGG
5' ss Score
9.2
3' ss Seq
CAATCTTTCTTTCCATCCAGGTG
3' ss Score
11.08
Exon sequences
Seq C1 exon
AAAATCCGTTCTAAAGTAGAGCTGGAAGTGCGTGACCTCCCTGAAGAGTTGTCTCTATCCTTCAATGCCACCTGCCTCAACAATGAGGTCATCCCTGGCCTCAAGTCTTGTATGGGACTCAAGATTGGAGACACG
Seq A exon
GTGAGGTGGGCTGGGCAGGGCCTTTGTCCTGGAGCATCTGTGGGCACCCAACCCCCTTTCTTCCTTTTGTAGTGACTAAAAATGGCCCCCTTCCACCAGAAAAAAAATATGGGCAAGAAAAATACGTTTCCTGAAAGTCATTCTAAGTTAGATGTAATGGATCCACCAATCTTTTCCTCTGAGGCTTCTGTTGCGTAAGCCATTTCTGTTACGTGAACTTCACTCTCAGGAATTTGAAAAACTTACAATTTGGTTACCTTTGTTTGTGTATGCACAGTTGATTGCAAAGGAAAATATTTCTTTACCTTCAGTCCCTCACCAGTCGCCAGCCTTTCCAAGGTAATTAATACCTTTCTTTTGTAAAACGACACAAGAAAGTAAAATCTAAAATGTAAAACACTCCAGTCTCTCCACGACTTTCCTTATTGGTCGTTTCTCCTCCGCTTCTGCCTAAGGGGAGAGGGGTTGGTGGGAGGGGAGGAAGGAGGGGAAGAAAATAGATCTTTGGATACGCTGATCCTTTCTATTGACCTATCTGTCTCTCAGGCACTTGTGCAAACATCCCATGTTAGAAATATTGTCCTGAAACATGCTTTATTGCATAAGCTATGAAATGTGTGGGAACTGAAGTAGATCCTGAGCTTATGATTGACCACCATGTGGGATTGTGTGGTGCAAAATAGTGCTTTGTGCATCTTGCTGATAATTATAATCAGGCCAAAGCAGGGTGTTTATATGATCACAGGTTCTGTTCAGTTTGAGCTGGTCTATTTCATATGTGGAGTGAAAAAACAGCCTTTTATTATTTATTGACTGTAAACCATGTCTCTGCATCCAGCTAGATATGTCACAACGATACTATTCCCGTGCTTGTGTTTTTGCTTTGCAGACCTTCATATAGGGAAGGCTGAGGAACTCCAGATTGCAAAAGCATAAGACACCCAATTTGGGTATTCCTTGGCAGGGCAGGGAACAACTTTTTTTTTCCTCCAGAGCTGGAGTGTTAACTGGGCCCAACTGTGTCTAAATACAATCTTTCTTTCCATCCAG
Seq C2 exon
GTGAGCTTCAGCATTGAGGCCAAGGTGCGAGGCTGTCCCCAGGAGAAGGAGAAGTCCTTTACCATAAAGCCCGTGGGCTTCAAGGACAGCCTGATCGTCCAGGTCACCTTTGATTGTGACTGTGCCTGCCAGGCCCAAGCTGAACCTAATAGCCATCGCTGCAACAATGGCAATGGGACCTTTGAGTGTGGGGTATGCCGTTGTGGGCCTGGCTGGCTGGGATCCCAGTGTGAGTGCTCAGAGGAGGACTATCGCCCTTCCCAGCAGGACGAATGCAGCCCCCGGGAGGGTCAGCCCGTCTGCAGCCAGCGGGGCGAGTGCCTCTGTGGTCAATGTGTCTGCCACAGCAGTGACTTTGGCAAGATCACGGGCAAGTACTGCGAGTGTGACGACTTCTCCTGTGTCCGCTACAAGGGGGAGATGTGCTCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000056345-ITGB3:NM_000212:9
Average complexity
IR-C
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:
NA
A:
NA
C2:
NA
Main Inclusion Isoform:
NA
Main Skipping Isoform:
NA
Other Inclusion Isoforms:
NA
Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
CGTGACCTCCCTGAAGAGTTG
R:
AGTCCTCCTCTGAGCACTCAC
Band lengths:
355-1405
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
Other AS DBs:
FasterDB (Includes CLIP-seq data)
AS-ALPS (AS-induced ALteration of Protein Structure, links to PINs)
APPRIS (Selection of principal isoform)
DEU primates (Only for human)