Special

HsaEX6030783 @ hg19

Exon Skipping

Gene
ENSG00000186377 | CYP4X1
Description
cytochrome P450, family 4, subfamily X, polypeptide 1 [Source:HGNC Symbol;Acc:20244]
Coordinates
chr1:47505014-47514301:+
Coord C1 exon
chr1:47505014-47505204
Coord A exon
chr1:47512139-47512272
Coord C2 exon
chr1:47514237-47514301
Length
134 bp
Sequences
Splice sites
3' ss Seq
TCCCTCCCTCATCCTCACAGGGA
3' ss Score
10.04
5' ss Seq
CAGGTCTTT
5' ss Score
2.36
Exon sequences
Seq C1 exon
GATGAAAGTGGTAGCAGCTTCTCAGATATTGATGTACACTCTGAAGTGAGCACATTCCTGTTGGCAGGACATGACACCTTGGCAGCAAGCATCTCCTGGATCCTTTACTGCCTGGCTCTGAACCCTGAGCATCAAGAGAGATGCCGGGAGGAGGTCAGGGGCATCCTGGGGGATGGGTCTTCTATCACTTG
Seq A exon
GGACCAGCTGGGTGAGATGTCGTACACCACAATGTGCATCAAGGAGACGTGCCGATTGATTCCTGCAGTCCCGTCCATTTCCAGAGATCTCAGCAAGCCACTTACCTTCCCAGATGGATGCACATTGCCTGCAG
Seq C2 exon
GGATCACCGTGGTTCTTAGTATTTGGGGTCTTCACCACAACCCTGCTGTCTGGAAAAACCCAAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000186377-'7-9,'7-8,9-9=AN
Average complexity
A_S
Mappability confidence:
100%=100=100%
Protein Impact

ORF disruption upon sequence exclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.016 A=0.000 C2=0.000
Domain overlap (PFAM):

C1:
PF0006717=p450=FE(13.8=100)
A:
PF0006717=p450=FE(10.0=100)
C2:
PF0006717=p450=FE(4.6=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:
AAGTGGTAGCAGCTTCTCAGA
R:
GGTTTTTCCAGACAGCAGGGT
Band lengths:
246-380
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains