Special

HsaINT0033957 @ hg19

Intron Retention

Gene
ENSG00000167123 | CERCAM
Description
cerebral endothelial cell adhesion molecule [Source:HGNC Symbol;Acc:23723]
Coordinates
chr9:131185147-131185542:+
Coord C1 exon
chr9:131185147-131185257
Coord A exon
chr9:131185258-131185424
Coord C2 exon
chr9:131185425-131185542
Length
167 bp
Sequences
Splice sites
5' ss Seq
CAGGTGGTG
5' ss Score
1.16
3' ss Seq
TCTCACCTCTATCCCCTCAGGTT
3' ss Score
11.06
Exon sequences
Seq C1 exon
GTGTGCCACGGACCACAATGTGGACAACACCACAGAGATGCTGCAGGAGTGGCTGGCGGCTGTGGGCGATGACTATGCTGCTGTGGTCTGGAGGCCTGAGGGCGAGCCCAG
Seq A exon
GTGGTGATCTGAGGGGAAGGGTGCTGGGGAAGATGGAGAACAGCTGCAGCCCAGAGAGGAAAAGGGACAGCCCAGAGCCACAGCCTCCAAGCCAGGGCTCTGTCCACTGCCCTGCAGAGAGGGAGGGGCATGTACCCCATGGGAACATCTCACCTCTATCCCCTCAG
Seq C2 exon
GTTCTACCCAGATGAAGAGGGTCCCAAGCACTGGACCAAAGAAAGGCACCAGTTTCTGATGGAGCTGAAGCAGGAAGCCCTCACCTTTGCCAGGAACTGGGGGGCCGACTATATCCTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000167123-CERCAM:NM_016174:2
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=0.108
Domain overlap (PFAM):

C1:
PF137041=Glyco_tranf_2_4=PU(30.4=96.0)
A:
NA
C2:
PF137041=Glyco_tranf_2_4=FE(48.8=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:
GTGCCACGGACCACAATGT
R:
CAGGATATAGTCGGCCCCC
Band lengths:
227-394
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