Special

HsaINT0044435 @ hg19

Intron Retention

Gene
ENSG00000162365 | CYP4A22
Description
cytochrome P450, family 4, subfamily A, polypeptide 22 [Source:HGNC Symbol;Acc:20575]
Coordinates
chr1:47607243-47607907:+
Coord C1 exon
chr1:47607243-47607287
Coord A exon
chr1:47607288-47607779
Coord C2 exon
chr1:47607780-47607907
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-CYP4A22:NM_001010969:3
Average complexity
IR-S
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


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
Conservation
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