Special

HsaINT0044497 @ hg19

Intron Retention

Gene
ENSG00000171954 | CYP4F22
Description
cytochrome P450, family 4, subfamily F, polypeptide 22 [Source:HGNC Symbol;Acc:26820]
Coordinates
chr19:15648346-15648804:+
Coord C1 exon
chr19:15648346-15648473
Coord A exon
chr19:15648474-15648682
Coord C2 exon
chr19:15648683-15648804
Length
209 bp
Sequences
Splice sites
5' ss Seq
CATGTGAGT
5' ss Score
7.83
3' ss Seq
ACCATGTATCTCTCTTCCAGGCT
3' ss Score
10.6
Exon sequences
Seq C1 exon
GGGATGGGCTGCTGCTCAGCAAAGGTGACAAGTGGAGCCGGCACCGTCGCCTGCTGACACCCGCCTTCCACTTTGACATCCTGAAGCCTTACATGAAGATCTTCAACCAGAGCGCTGACATTATGCAT
Seq A exon
GTGAGTCCTAAGGCTTTGAGGGAAGAGGGTGTCTTGGGAGTGAGGCTGGTCCAGGCTCCAACTCATGCATGGGCAAGCCATGTGATGTCAGGAGCCCTCACTGACTTTATCTATAAAATGAGCTTGTAGTGAAAACGCAGTCGGGTCCTTGTTAGGCTGACTCCCTCTCTGTGGTTTCCATGCACAGTCACCATGTATCTCTCTTCCAG
Seq C2 exon
GCTAAATGGCGGCATCTGGCAGAGGGCTCAGCGGTCTCCCTTGATATGTTTGAGCATATCAGCCTCATGACCCTGGACAGTCTTCAGAAATGTGTCTTCAGCTACAACAGCAACTGCCAAGA
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000171954-CYP4F22:NM_173483:6
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(9.0=100)
A:
NA
C2:
PF0006717=p450=FE(8.6=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
TGCTCAGCAAAGGTGACAAGT
R:
TCTTGGCAGTTGCTGTTGTAG
Band lengths:
238-447
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