Special

HsaINT0044335 @ hg38

Intron Retention

Gene
ENSG00000073067 | CYP2W1
Description
cytochrome P450 family 2 subfamily W member 1 [Source:HGNC Symbol;Acc:HGNC:20243]
Coordinates
chr7:983199-984574:+
Coord C1 exon
chr7:983199-983385
Coord A exon
chr7:983386-984411
Coord C2 exon
chr7:984412-984574
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:ENST00000308919:1
Average complexity
IR
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


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
Conservation
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