Special

HsaINT0149362 @ hg19

Intron Retention

Gene
ENSG00000097033 | SH3GLB1
Description
SH3-domain GRB2-like endophilin B1 [Source:HGNC Symbol;Acc:10833]
Coordinates
chr1:87200285-87200862:+
Coord C1 exon
chr1:87200285-87200374
Coord A exon
chr1:87200375-87200761
Coord C2 exon
chr1:87200762-87200862
Length
387 bp
Sequences
Splice sites
5' ss Seq
CATGTGAGT
5' ss Score
7.83
3' ss Seq
ACTATAATTTTCCTTCACAGGCC
3' ss Score
10.51
Exon sequences
Seq C1 exon
TCTGAACAGGAATTAAGAATAACTCAAAGTGAATTTGATCGTCAAGCAGAGATTACCAGACTTCTGCTAGAGGGAATCAGCAGTACACAT
Seq A exon
GTGAGTATTCATTCATTGGAAATTCATTTGGAACAAGACTTTGGTAGTCCTAAGGCAATTTTGGGAGGAAAAACTGAACTTTTCAGTCATTCATCAAGGAAATTTAAATTGTTCTACTTTCCAATATATCCGAATAAATATTTTAAATTGTTGTTTACATCTTATCACCGAGTTCTCCCACCCTCATTAAATATACATGTTGTTGTTTATTGGCTAAGCAGAGTTTGCTAGTGTACTATTCACGAAGGCCAATCTTAATAAGCCTTGTAGTAAAATGTTAGATACTGGTGAGTCTACCTCAGTACAATATTGTGGTCTGTCTCCCCCTTGCATTTGCCATTTAAGTTGACTATACAGCTAAGAACTAACTATAATTTTCCTTCACAG
Seq C2 exon
GCCCATCACCTTCGCTGTCTGAATGACTTTGTAGAAGCCCAGATGACTTACTATGCACAGTGTTACCAGTATATGTTGGACCTCCAGAAACAACTGGGAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000097033-SH3GLB1:NM_016009:6
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.156 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF0311413=BAR=FE(11.8=100)
A:
NA
C2:
PF0311413=BAR=FE(13.4=100)


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