Special

HsaINT0149362 @ hg38

Intron Retention

Gene
ENSG00000097033 | SH3GLB1
Description
SH3 domain containing GRB2 like endophilin B1 [Source:HGNC Symbol;Acc:HGNC:10833]
Coordinates
chr1:86734602-86735179:+
Coord C1 exon
chr1:86734602-86734691
Coord A exon
chr1:86734692-86735078
Coord C2 exon
chr1:86735079-86735179
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:ENST00000370558:6
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.192 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


Other Skipping Isoforms:
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