HsaINT0145204 @ hg19
Intron Retention
Gene
ENSG00000133812 | SBF2
Description
SET binding factor 2 [Source:HGNC Symbol;Acc:2135]
Coordinates
chr11:10019813-10022569:-
Coord C1 exon
chr11:10022461-10022569
Coord A exon
chr11:10019927-10022460
Coord C2 exon
chr11:10019813-10019926
Length
2534 bp
Sequences
Splice sites
5' ss Seq
CTTGTAAGT
5' ss Score
8
3' ss Seq
AATTTTTTTATCTCTTTCAGTTA
3' ss Score
9.78
Exon sequences
Seq C1 exon
TTATCCTTATATCCCTATTCTCCCGGCTCAGCTACTGGAAGTTCTAAGTTCCCCAACGCCTTTCATTATTGGAGTACATTCTGTCTTTAAAACTGATGTCCATGAACTT
Seq A exon
GTAAGTATTCATCTTTAAAGTTTCCAGTTATTGAGTCCAGAAGTTTATCATATTTCTTTGGGTCCTATAACATTTCAACTCATCACTATTTTCAGATCTGTAGCATTTCCAGTAGAAAAGATTGGATAGAAGAAAAATATCATTGAAAAGTCTGTATATTAATTTTGCCATATAGCAAGTATAGGAGGTTTTATAAAGGAATTTATTAATATTTTTAAATATCCCTCTTTTGGTACATTGTTTATCTTTATTATTCATCTTACATATGACAAAAGATAAAATTCTATTTATACTTTTGATATTAGTGCATAATTGTTTTATATTTTGAAGTGAGACGTGTCTTGATACCAAATTCCTGATAACTAACAAAGCAGAAAGCATATGCAAAAGAGTGAAGAGTTTTAGTGGAACAGAAGTTTGGTATGAGCTTCCACGAAATTTTTGTATTCTTAATGCCATATGAATAGAAGAAGCAAAAGTATACTCTATATTCAAGCCAGTTCTGGAATAATTCATTTAGTTCTGTGTATCACACTTTATGAGGGACTGTAACAAAATAAAGCACATCAGAAAAGGACATCCAGGATTATCAAGTATTTAGAAACTATGTTCTGTAAGGGCCTAAGGAAATTTTCTCAGGTAATAATCTGATACTATTTGATAGGTAAAAGTAAGTATTTAAGTTACTGTCATAGAAGAAGGGTTGAGATTCATTTTTTGTAACTCTAAAAGGCTGAAATAAAATCAGTGGATGAAGTGGCTATAGAAACAGATTTCTGCCCAGTAAAAGTGTTTCCAACAATTAGAACTGCCTGGTTATGGAATGGATTTCCTTATGTGAGATGAGGAGTGTACTCTCAAGCACTGTAAGTAGAGTGTAAGGAAAAGATTATGTGACACTTTTCAGAGAGCCTGAGAAAAATTCTTCACTGTAAAGTTAGGCTGCATAGCATCTATGATCCACAGATCCCTAAGATTTTGTAATTCTTCTTCTGTTTTAGTTTTAAATGCCAGCAAAGAAGTAATTATAGTTGTAACCAAATCAGAGGTGTCATTTAAACTAACAAAATATTATTTAACATTATAATTATAAGCAGGACTTTCATTCGTATAGTCATCATTCTTTCTAACTTTATATGTTGATACTTAGTTCCTATTTAATTTTGGTATCACTGTATAAAAATATGTGTAAATCAATAAACATTTAATAAAACCTAATTAATACTAGTTAGAAGCATATCCACCTGGTTTGTACATAATTTTATTTCTGCTAAATATAAACAGTCACTGGAGGCCAGGCACGGTGGCCCACACCTGTAATCCTAGCACTTCGGGAGGCCAAGGCAGGCGGATCACCTGAGGTCAGGAGTTTGAGACCACCCTGGCCAACATGGAGAAACCCTGTCTCTACTAAAACTACAAAAAATTAGCTGGGTGTGGTGGTGCATGCCTGTAATCCCAGCTACTCAGGAGGGTGAGGCAGGAGAATCACTTGAACCTGGGAGGTGGAGGTTGCAGTGAGTCAAGATTGCACCACTATACTCCAGCCTGGGCGAGAGTAAGACTCTGTCTCAAAAATAAATACATACATACATACATACATACATACATACATACATACATACATACATACAGTCACTGGAGGTAGGACCAACCAAGTGTTGCCAAATAAATAAAAACAGTCGCTGGAGGTAGGACAAACCAAGTGTTGCCAAATGCAAATTTCTTAAAATCGTAATGAATAAATTAGAATGAAGTATAATATTGTCAATATAACAACTTCACTCATCTTGGTTGTTTTCTCTTACACTTTTATGTAAGTTATTTTTAAATAGACTTTTGTAAAATGCTAAAGATCAGCTTTTTCTAAGTGGCTAAACAGCACCCTTTTGATGTATACTAATTGTTAATTCTTATAATAAATACTAATTTTTTTAGAATATTACTAAACTACTTGAATAAAGTGTCTCAAATGCAATCCTCTGTGCTTGCTGCAGCAGCATATATAGTAAAATCAGAACAAAATGCAATGGCTCAAACAAAATAAAGTGTTATCGAACATTCATGCAGCAGTCCATAGAGATGTTCCATTATGCCAGACCAGTTTGCTCTATGAAGTCACTCAAGATCCAAGTTTCCTTCCTTCTTGTTTCTCCAACAGAATCCTCCCAGGCATTGTCATCATGTGTATGCTGAAGGCTGGTTTGCTGCCAGTTAATAATTTCAGTCTAAGGGAAAAGGAAAGACAGCATAGGAGAGCTTTACATATCCCCTGTCTTGAAGGACAGGAAAACACATGTCACTTCTCATGTTTTATTGGCAGAATCTTAGCCACATGCCACACTTAATTTCAAAGGAACCTGGGAAATACAGGGTAGGTGGGAACTTGTTAGCCCAGAATTCTACTACTATGGACAAACAAGAGTCTCTTCCACATCTGATTCTTCTCGTTTTGAATTAGTCAAGGGAAAAATAATTTGCTTAACAACAAATGTATTTTGGTAATTATAGGTTAATTTTTTTATCTCTTTCAG
Seq C2 exon
TTAGATGTAATCATAGCAGATTTGGATGGAGGCACTATTAAAATTCCCGAATGTATTCACCTCTCTTCCCTCCCAGAACCACTTCTACATCAGACTCAATCAGCTCTTTCTTTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000133812-SBF2:NM_030962:8
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:
PF0214116=DENN=FE(19.7=100)
A:
NA
C2:
PF0214116=DENN=PD(5.5=26.3)
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)