Special

HsaEX6006791 @ hg38

Exon Skipping

Gene
ENSG00000073067 | CYP2W1
Description
cytochrome P450 family 2 subfamily W member 1 [Source:HGNC Symbol;Acc:HGNC:20243]
Coordinates
chr7:984950-986797:+
Coord C1 exon
chr7:984950-985099
Coord A exon
chr7:985166-985323
Coord C2 exon
chr7:986624-986797
Length
158 bp
Sequences
Splice sites
3' ss Seq
GAGGCCCGTCTCCCTCGCAGGCC
3' ss Score
7.86
5' ss Seq
CAGGTGAGG
5' ss Score
10.07
Exon sequences
Seq C1 exon
GCATCTTCTTCTCATCTGGGGCGCGCTGGAGGGCTGCCCGCCAGTTCACGGTGCGTGCCCTGCACAGCCTGGGCGTGGGCCGGGAGCCGGTGGCTGACAAGATTCTGCAGGAGCTGAAATGCCTCTCTGGGCAGCTGGATGGCTACAGAG
Seq A exon
GCCGGCCCTTCCCGCTGGCCCTACTGGGCTGGGCTCCCTCCAATATCACCTTCGCGCTCCTCTTCGGCCGCCGATTTGACTACCGGGACCCCGTGTTTGTGTCCCTGCTGGGTCTCATCGATGAGGTCATGGTCCTCTTGGGGTCCCCTGGCCTGCAG
Seq C2 exon
CTGTTCAACGTCTACCCATGGCTCGGGGCCCTGCTCCAGCTGCACCGGCCCGTCCTGCGCAAGATCGAGGAGGTCCGTGCCATTCTGAGGACCCTCCTGGAGGCGCGGAGGCCCCACGTGTGCCCGGGGGACCCCGTGTGCAGCTATGTGGACGCCCTGATCCAGCAGGGACAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000073067-'2-7,'2-2,3-7=AN
Average complexity
A_C1
Mappability confidence:
100%=100=100%
Protein Impact

ORF disruption upon sequence exclusion

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

C1:
PF0006717=p450=FE(11.0=100)
A:
PF0006717=p450=FE(11.4=100)
C2:
PF0006717=p450=FE(12.5=100)


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Inclusion Isoforms:


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GCATCTTCTTCTCATCTGGGGC
R:
GTCCTCAGAATGGCACGGAC
Band lengths:
242-400
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains