Special

HsaINT0149372 @ hg19

Intron Retention

Gene
ENSG00000148341 | SH3GLB2
Description
SH3-domain GRB2-like endophilin B2 [Source:HGNC Symbol;Acc:10834]
Coordinates
chr9:131772399-131772972:-
Coord C1 exon
chr9:131772949-131772972
Coord A exon
chr9:131772489-131772948
Coord C2 exon
chr9:131772399-131772488
Length
460 bp
Sequences
Splice sites
5' ss Seq
AAGGTAAGT
5' ss Score
11
3' ss Seq
GGCTGCCCTGCCCTGCCCAGGCC
3' ss Score
6.96
Exon sequences
Seq C1 exon
CTCTGGAATGATGAAGTGGACAAG
Seq A exon
GTAAGTTGGGGCCTGGGGGGCTGGGCTCGAGGAAGAAGGGGTGGCGGGGTGCAGGCACACTTGCTGCTGTGGGGTCTGATCTGTTTCTCACTCTGCCCCACACCCACTGGGGAGGGGTTACTGCTTTCCCTCCCTGGGCCTCAGTTTCCCCTCTGTGGGGAAATGTTTTCTCCACAGTACCCTGTAGCACACAGTAGGCCCTCAGGATGCACTTGCTGGGTGGATTTCTCCGATGGGTGATGGAGGAAGGGTCTGTCACTGCAGCTGCCTGTGGGGTCCTGAGTGGGGCTCTAGCTTCTCTGGGGTTGGGGCTCCAGGTGTGAAGTCAGGCATAGACCCAGAAGGCTCTCTGTGTTCCCAGGGGAAAGGGACAGGCGGCTCCCAGGTAGGCTCCAGGAGAAGACTGCGGGGAAGCTGGTGGGTGGTGTGTGGGTGCTCATGGCTGCCCTGCCCTGCCCAG
Seq C2 exon
GCCGAGCAGGAGCTCCGCGTGGCCCAGACAGAGTTTGACCGGCAAGCAGAAGTGACCCGTCTCTTGCTGGAGGGAATCAGTAGCACTCAC
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000148341-SH3GLB2:NM_020145:7
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=0.167
Domain overlap (PFAM):

C1:
PF0311413=BAR=FE(2.7=100),PF0313112=bZIP_Maf=FE(7.8=100)
A:
NA
C2:
PF0311413=BAR=FE(11.4=100),PF0313112=bZIP_Maf=PD(24.4=73.3)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
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