Special

HsaINT0044448 @ hg38

Intron Retention

Gene
ENSG00000142973 | CYP4B1
Description
cytochrome P450 family 4 subfamily B member 1 [Source:HGNC Symbol;Acc:HGNC:2644]
Coordinates
chr1:46813482-46814063:+
Coord C1 exon
chr1:46813482-46813606
Coord A exon
chr1:46813607-46813911
Coord C2 exon
chr1:46813912-46814063
Length
305 bp
Sequences
Splice sites
5' ss Seq
CAGGTCAGG
5' ss Score
7.2
3' ss Seq
TCCTACCCTCTGCTTAGCAGGGA
3' ss Score
4.95
Exon sequences
Seq C1 exon
GACAAGTGGGAAGAGAAAGCTCGGGAGGGTAAGTCCTTTGACATCTTCTGCGATGTGGGTCACATGGCGCTGAACACACTCATGAAGTGCACCTTTGGAAGAGGAGACACCGGCCTGGGCCACAG
Seq A exon
GTCAGGAGCCACCTCGGGGCTGACCGCACTGTCTCCAAAGCCATCTTAGAGGGGAGAGTTGGCAGGGGTCCTGGGCTCTGATCTGAGAAGAGATAGGGTCCTGCCCCAGGGAGCCTTAGCTTGCGGGGAGACAGGACCTGCTCATGGTGGGGTAAACACCTGGCTTTAGCAAGGAGGCTTAAGGGCAGGGAGAAGAAGAGCAGGATGCTCTGTGGTTGGGGCTAGATTCCTGGAATGGAGTTTCTCTGGCTCTGCTCCTGGGCCAGTGTCTAAGCCAATCCCTCCTCCTACCCTCTGCTTAGCAG
Seq C2 exon
GGACAGCAGCTACTACCTTGCAGTCAGCGATCTCACTCTGTTGATGCAGCAGCGCCTTGTGTCCTTCCAGTACCATAATGACTTCATCTACTGGCTCACCCCACATGGCCGCCGCTTCCTGCGGGCCTGCCAGGTGGCCCATGACCATACAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000142973:ENST00000271153:5
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=0.011
Domain overlap (PFAM):

C1:
PF0006717=p450=FE(25.0=100)
A:
NA
C2:
PF0006717=p450=FE(11.2=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
TGGGAAGAGAAAGCTCGGGAG
R:
CTGTATGGTCATGGGCCACCT
Band lengths:
271-576
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