HsaINT0044435 @ hg38
Intron Retention
Gene
ENSG00000162365 | CYP4A22
Description
cytochrome P450 family 4 subfamily A member 22 [Source:HGNC Symbol;Acc:HGNC:20575]
Coordinates
chr1:47141571-47142235:+
Coord C1 exon
chr1:47141571-47141615
Coord A exon
chr1:47141616-47142107
Coord C2 exon
chr1:47142108-47142235
Length
492 bp
Sequences
Splice sites
5' ss Seq
TTGGTATGT
5' ss Score
7.12
3' ss Seq
CATATTCGTGTCTACCTTAGGGT
3' ss Score
9.32
Exon sequences
Seq C1 exon
ACCCGAAATCCCATGGATCCTACAAATTCCTGGCTCCACGGATTG
Seq A exon
GTATGTGTGCAAACTAGGACTGCAGCCCACTCCCTAGTTAGGTTTGAGTTATTTATTTGGCTCACAGAGAACAACAGATTAGAGGCCACCACTATCATGACCTCATCCCCAAATCAAGCCTCATTTCCCTCTTCTAACAAGACCCTCACCCCTTCCTAATGCTGGTGCAAACCTTCCTGAGGCTCAGCTTCTTCCATTTCATGTCTCAGTTCTCTCCAGACATCCTTGGCTTCACATTTATTTTACATCTGCCCACAACCCTTTTCAACCTTTATCTCACAGCTGTCATAATCACATGGATGTAGCAGCTCAATTAGAAAATTCACATGCCTGAAATATACCTCCTTTTCCTGCATTTGCCCATGATGTGGCTTCTTCTGGATAGTTCTTCCCCCAGGAAGCCACCTTTCTCCCTCCCAAATTGTCACCAGTCATCCCTAGGTCCGTGCAGCCTCTGATACACACACATACACATATTCGTGTCTACCTTAG
Seq C2 exon
GGTACGGCTTGCTCCTGTTGAATGGGCAGACATGGTTCCAGCATCGACGGATGCTGACCCCAGCCTTCCACAATGACATCCTGAAGCCATACGTGGGGCTCATGGCAGACTCTGTACGAGTGATGCTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000162365:ENST00000371891:3
Average complexity
IR
Mappability confidence:
NA
Protein Impact
ORF disruption upon sequence inclusion
No structure available
Features
Disorder rate (Iupred):
C1=0.000 A=NA C2=0.000
Domain overlap (PFAM):
C1:
PF0006717=p450=FE(3.7=100)
A:
NA
C2:
PF0006717=p450=FE(10.4=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:
No suggested primer sequences
R:
No suggested primer sequences
Band lengths:
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