HsaINT0044336 @ hg19
Intron Retention
Gene
ENSG00000073067 | CYP2W1
Description
cytochrome P450, family 2, subfamily W, polypeptide 1 [Source:HGNC Symbol;Acc:20243]
Coordinates
chr7:1024048-1024735:+
Coord C1 exon
chr7:1024048-1024210
Coord A exon
chr7:1024211-1024585
Coord C2 exon
chr7:1024586-1024735
Length
375 bp
Sequences
Splice sites
5' ss Seq
GAGGTCGGT
5' ss Score
5.44
3' ss Seq
CGCACTGTATCTGCCTACAGGCA
3' ss Score
8.73
Exon sequences
Seq C1 exon
CTCTCAGAACGCTACGGGCCGGTGTTCACCGTGCACCTGGGGCGCCAGAAGACGGTGGTGCTGACGGGGTTCGAGGCGGTCAAAGAGGCGCTGGCGGGCCCCGGGCAGGAGCTGGCCGACCGGCCTCCCATCGCCATCTTCCAGCTCATCCAGCGAGGTGGAG
Seq A exon
GTCGGTGTGTGGCCGGCGCTACGGGGCCTACTGGGTGTGGGGGCACCTGGACCCCAGGAGGGGTGGGGGCTCCAGCAGCGGGAGAGGCTCCCAGGGTGGCCTGGGGAAGAGCAGGCAGGAGCTGGGCCTCCGGGCTGGTGCTGAGAAGGGCCAGGTGTCCACACAGCAGGTCAGGTGCTCAGAACCAGCAAGCGGGGTTCTTTTCATCCCAAGTCAAGAGGGGCCAGGGCCAGCCCAGGGGGACGGGAGTGGGGATGGGGGTGAGGGCCCAGCCAGTCTCGCTGCCCTGTCAGCCTGCTCACTTCCTGCCCACTTGCCTGGCGGGGCTGGCTGGGGTGGGAACCTGGGCTCACCACGCACTGTATCTGCCTACAG
Seq C2 exon
GCATCTTCTTCTCATCTGGGGCGCGCTGGAGGGCTGCCCGCCAGTTCACGGTGCGTGCCCTGCACAGCCTGGGCGTGGGCCGGGAGCCGGTGGCTGACAAGATTCTGCAGGAGCTGAAATGCCTCTCTGGGCAGCTGGATGGCTACAGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000073067-CYP2W1:NM_017781:2
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact
Alternative protein isoforms
No structure available
Features
Disorder rate (Iupred):
C1=0.000 A=NA C2=0.000
Domain overlap (PFAM):
C1:
PF0006717=p450=FE(11.9=100)
A:
NA
C2:
PF0006717=p450=FE(11.0=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:
CTCTCAGAACGCTACGGGCC
R:
CTCTGTAGCCATCCAGCTGC
Band lengths:
313-688
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)