Special

HsaINT0037728 @ hg19

Intron Retention

Gene
ENSG00000188986 | COBRA1
Description
cofactor of BRCA1 [Source:HGNC Symbol;Acc:24324]
Coordinates
chr9:140161396-140161798:+
Coord C1 exon
chr9:140161396-140161538
Coord A exon
chr9:140161539-140161691
Coord C2 exon
chr9:140161692-140161798
Length
153 bp
Sequences
Splice sites
5' ss Seq
TAAGTACGG
5' ss Score
2.1
3' ss Seq
TGATGGCGCCCCGGGCGCAGGTT
3' ss Score
4.5
Exon sequences
Seq C1 exon
GAGGTAGAGCTCATCACCAGGTTCCTCCCGATGCTCATGTCCTTCCTGGTGGATGACTACACTTTCAATGTGGATCAGAAACTTCCGGCTGAGGAGAAAGCCCCAGTCTCATATCCAAACACACTTCCCGAAAGCTTCACTAA
Seq A exon
GTACGGGCTGTAGGGCCATGGTGCAGGGGTGGCCGTGGCGCAGGGATGGCACTGTTGCCCAGGGGGCTGCCTCAGGGCTGGGCAGGGGTCGGTGTGGGGCTGAGGTGGGGCTGAGGTGGGGCTGAGGTGGGGCTGATGGCGCCCCGGGCGCAG
Seq C2 exon
GTTTCTGCAGGAGCAGCGCATGGCCTGCGAGGTGGGGCTGTACTACGTCCTGCACATCACCAAGCAGAGGAACAAGAACGCGCTCCTCCGCCTGCTGCCCGGGCTGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000188986-COBRA1:NM_015456:9
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.021 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF062098=COBRA1=FE(9.9=100)
A:
NA
C2:
PF062098=COBRA1=FE(7.6=100),PF069126=DUF1275=PU(19.6=29.7)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
AGGTAGAGCTCATCACCAGGT
R:
GAGCGCGTTCTTGTTCCTCTG
Band lengths:
227-380
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