HsaINT0044335 @ hg19
Intron Retention
Gene
ENSG00000073067 | CYP2W1
Description
cytochrome P450, family 2, subfamily W, polypeptide 1 [Source:HGNC Symbol;Acc:20243]
Coordinates
chr7:1022835-1024210:+
Coord C1 exon
chr7:1022835-1023021
Coord A exon
chr7:1023022-1024047
Coord C2 exon
chr7:1024048-1024210
Length
1026 bp
Sequences
Splice sites
5' ss Seq
GAGGTAAGT
5' ss Score
11.08
3' ss Seq
ACCCCCGCCATCCCTGCCAGCTC
3' ss Score
7.23
Exon sequences
Seq C1 exon
CAGCCACGTCCTCATGGCCCTGCTGCTCTTGCTGTTCCTGGGCCTCCTGGGGCTCTGGGGGCTGCTCTGCGCCTGCGCCCAAGACCCCTCCCCAGCTGCCCGGTGGCCCCCGGGGCCTCGCCCGCTGCCGCTCGTCGGGAACCTGCACTTGCTGCGTCTGTCGCAACAGGACCGGTCCCTGATGGAG
Seq A exon
GTAAGTCAGGGAGCCCGGGCAGCTCTTGCCGCTTGGACAGCTGCCGTGTCCTGGCCCCCCTCCTGGGGAAGCCCAGCCCGGTTTCCACTGCCTGTTCCCACATGGTGCCGGGCCCAGCGGGGCACGCAGGAGGCCGGAGGGCCCACCCTGCTTTTGGGAGGGGAAAGCCACCCCGTCCCACAGGGAAGCAGACACACTGAGTACGAAGAAGCCCTGGAGGTGCCACCCAGGGCCCGGCGCGGGAGCAGGAGTCTGGAGGGCTCCCTGGAGGCGGTGGCGTCTGCTGAGAGCCCGCAGGAGGCCAGGCTTAGGGACAGCAGAGGGGAGGAGGGCCTGGGCCTGTCGGCTGCCTGCTCAGCCCCCCTCGGCCCTCAGGTGTTCAACAGCAAACACTTCCCACTTTTGAGCCTCTGTTTCCTCATCTGTGAAATGGGAAGAGGACCTGTGCCTCCTGGGCAGGGATGCTGAGGACAGAGGGTACGGGGACACGGCACGGGGCAGCCTGACTAGCACTGTCGCTCTGTCCTCGCTCAGGCAGGCAGGGTCAGTGGGACAGGGCTGACCAGTCAGGCCCGGGCCCTGCCTCCGGCTGCCCCCAACTGCGGGCTGGGGTGCTGCTGGCCGGGCTGTAGCCGAAGACGGATCAGGGTCTCTGGGGGCCGAGCCTGTCAGGCCCTCACTCTGTGCAGACTCTGGCCTTTCAGAATGTGCCACCCCAGCAGACAGCCAGCCCCCGACCTTGCCGCCTGGACTCAGGGCTTGAGCCCCCCAGGAATTTTGGCTAAAAAGAAAATCCCACAACAGCCATGCCAAGCACCAGATGGCGAGAGGGCTCTGTGGGCTCCAGGCTGGGCGCTGCCCCCTCCACCCTGCACCACTGGCTTTATGGCATCTAGGCGTGCCCCCTCCACCTGCCCCCATTTTCCCTCTGTCCCCACCCCTACCCAGCACAGGCCCGGCCTGAGGGGACCTAAGGGGGGTCTTGTGGGTGAGGGCTGCCCGGGTGACCCCCGCCATCCCTGCCAG
Seq C2 exon
CTCTCAGAACGCTACGGGCCGGTGTTCACCGTGCACCTGGGGCGCCAGAAGACGGTGGTGCTGACGGGGTTCGAGGCGGTCAAAGAGGCGCTGGCGGGCCCCGGGCAGGAGCTGGCCGACCGGCCTCCCATCGCCATCTTCCAGCTCATCCAGCGAGGTGGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000073067-CYP2W1:NM_017781:1
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact
ORF disruption upon sequence inclusion (1st CDS intron)
No structure available
Features
Disorder rate (Iupred):
C1=0.051 A=NA C2=0.000
Domain overlap (PFAM):
C1:
PF0006717=p450=PU(5.7=44.8)
A:
NA
C2:
PF0006717=p450=FE(11.9=100)
Main Inclusion Isoform:
NA
Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
CCACGTCCTCATGGCCCT
R:
CCTCGCTGGATGAGCTGGAAG
Band lengths:
342-1368
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
Other AS DBs:
FasterDB (Includes CLIP-seq data)
AS-ALPS (AS-induced ALteration of Protein Structure, links to PINs)
APPRIS (Selection of principal isoform)
DEU primates (Only for human)