HsaINT0017370 @ hg19
Intron Retention
Gene
ENSG00000186716 | BCR
Description
breakpoint cluster region [Source:HGNC Symbol;Acc:1014]
Coordinates
chr22:23613719-23615320:+
Coord C1 exon
chr22:23613719-23613779
Coord A exon
chr22:23613780-23615267
Coord C2 exon
chr22:23615268-23615320
Length
1488 bp
Sequences
Splice sites
5' ss Seq
AAAGTGAGT
5' ss Score
8.4
3' ss Seq
CCTCCCCTCTCTCTCCACAGCTC
3' ss Score
14.45
Exon sequences
Seq C1 exon
AACCTGAGAGCCAGAAGCAACAAAGATGCCAAGGATCCAACGACCAAGAACTCTCTGGAAA
Seq A exon
GTGAGTTCTGCATGCTGAGGTCTCTGTGTGCCCTCGTCAGGGAGGCTGCTGCTGGCAGAGGGGGCGTTGTGGAAAAGCAGACACAGTGCCCACTTGGGTCATCCCTTGGTGCCTTCCCTGTTCTCTCTTCAGATAGAGTGGGCACGAGGAAAGAACAGCTCAGGGAGGGCAGGGAAGGATACCATCAGGACCAGTTTGCCACCAACATTAGCAACAAGGTGCTGCTTAAATTGACTTAAATGTTATCCTGTTGACCCCAGTGGCCTCATAAGGAGGATTTTTTTTTTTTGAGGCGGAGTTTTGGCTCACTGCAACCTCCACTTCCCGGGTTCAAGTGATCCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCACACACCACCACAGCCAGCTAATTTTTGTATTTTTAATAGAGATGGGGTTTCCCTCCGTATTGGTCAGGCTTGTCTGAACTCCTGACCTAAAGTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCTACCGCACCTGGCAGTAACAAGGATTTTATTTTCTGTTTTTGCCAATGACAAGTTTGGTCATAAAGTAATCTGTGCAGAGCACAGGCTTTAAGTGGCTGGGCAGGAATTGAGTCCAGAGTTGCTGGGAAAGTGCTGTCAGGAATTGTCAGTCACTTCTTATTTTCAGTTGTTAGGGTGTTGTGAATAGTTACACTTGCAAAGAACAGCAGCCCCCGGAGCTTTGTCCTCCAAGCCTCAGTTTCCCTATCTGCAAAATGAAAATAGCGATGAGTGCCTTATGCTGGTTGTGGGAGTCTTGTGAAGAACATACTTGGCATGTCTCAGAACACACCTGAGCGTCTGTGCCTGGGACGGGCCACACTCACTGTCATCATGGAGAAGCACGGGTGGCTGAGGCTGGCCAGGGCTCCCACCATGCCAGGGAGTTGCTCCCACTGCAGTGGGGCTCATGTGCCTCTGGAGTCCGGGTGTCCTCGGGCAGGTCGCCAGAGAACCTGTCAAACCAAGAGTTGTATTGGCATCTGAGTAGGTTTCTGCTTGTCTCAGAGTCAGGTGTCTGAAATGTCCTGGGATCGATGGTAAGAGCAGCTAAGAGGTCTGCTCAGCTTACCCTCTGGGCTGGGGAGCAGGTCTCCCTCCAGAATTGGGGCCCACCCCAGCCCGTCCTTGCCAGGGTGGGTTCCCTGACCTCAGGCTAGAGGAGCAGCAGTGCTGAGCCTTTTCAGCTGTTGCCACCGAGCCAGCCATGCAGGCTCGGGTCTGACAGCCGCTCTGGACTCTGCATGCAGTGAATGTCCTGGACTTAAAGTGTTCCTGTTGGGTGCTCTAGCCTTGCCCTTGTCACTGCGCAGAGGGGAGATGGGGCCTGTGGAGGCTGGGGCAGCCCCCTCCCCACTCACCCTTGCACCGAGGGTGGTCAGGCAGCTGGTGTGCTTCTCCATGTGCAACCTCTCTCACCTCCCCTCTCTCTCCACAG
Seq C2 exon
CTCTGCTCTACAAGCCTGTGGACCGTGTGACGAGGAGCACGCTGGTCCTCCAT
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000186716-BCR:NM_021574:6
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact
ORF disruption upon sequence inclusion
No structure available
Features
Disorder rate (Iupred):
C1=0.571 A=NA C2=0.000
Domain overlap (PFAM):
C1:
PF0062115=RhoGEF=PD(8.7=38.1),PF0062115=RhoGEF=PU(28.6=95.2)
A:
NA
C2:
PF0062115=RhoGEF=FE(24.3=100)
Main Inclusion Isoform:
NA
Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
No suggested primer sequences
R:
No suggested primer sequences
Band lengths:
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)