Special

HsaINT0066545 @ hg38

Intron Retention

Gene
Description
far upstream element binding protein 1 [Source:HGNC Symbol;Acc:HGNC:4004]
Coordinates
chr1:77966694-77966955:-
Coord C1 exon
chr1:77966884-77966955
Coord A exon
chr1:77966752-77966883
Coord C2 exon
chr1:77966694-77966751
Length
132 bp
Sequences
Splice sites
5' ss Seq
CTGGTAATG
5' ss Score
5.67
3' ss Seq
CTGTTTGTTTTAAATTGTAGACA
3' ss Score
8.87
Exon sequences
Seq C1 exon
TAATTGGCAGAGGAGGTGAACAGATCTCACGCATACAACAGGAATCTGGATGCAAAATACAGATAGCTCCTG
Seq A exon
GTAATGTTACATTCTCATGGTATTTTCAGTGTGACTAGAAAACTAGCTTTTTTTTTTTTTTAAGCCTTCTAGTAACAATAATGCTACTTTTAATCTTTTGACCTGAAGTTATCTGTTTGTTTTAAATTGTAG
Seq C2 exon
ACAGTGGTGGCCTTCCAGAAAGGTCCTGTATGTTAACTGGAACACCTGAATCTGTCCA
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000162613:ENST00000294623:6
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.560 A=NA C2=0.767
Domain overlap (PFAM):

C1:
PF0001324=KH_1=FE(38.1=100)
A:
NA
C2:
PF0001324=KH_1=FE(30.2=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:
TAATTGGCAGAGGAGGTGAACA
R:
TGGACAGATTCAGGTGTTCCAG
Band lengths:
130-262
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