Special

HsaINT0065330 @ hg19

Intron Retention

Gene
ENSG00000137942 | FNBP1L
Description
formin binding protein 1-like [Source:HGNC Symbol;Acc:20851]
Coordinates
chr1:93988901-93989880:+
Coord C1 exon
chr1:93988901-93989048
Coord A exon
chr1:93989049-93989817
Coord C2 exon
chr1:93989818-93989880
Length
769 bp
Sequences
Splice sites
5' ss Seq
ATGGTAATT
5' ss Score
6.49
3' ss Seq
GCCGTGGTTATAATCTTCAGCAT
3' ss Score
4.25
Exon sequences
Seq C1 exon
GTTTACCTCGTGTGTAGCCTTTTTTAATATCCTTAATGAGTTAAATGACTATGCAGGACAGCGAGAAGTTGTAGCAGAAGAAATGGCGCACAGAGTGTATGGTGAATTAATGAGATATGCTCATGATCTGAAAACTGAAAGAAAAATG
Seq A exon
GTAATTCTTACAATTTTCATCCAATTGCAATAGTATATGAAATAGTCACACAGAAACACTTTGTTTTCTTTAAAATGTGTGTTCAGCATAAACTGGTTTTTCTATTTCACTACATTTCTTCTAGCTAAAAATTATCACAAAATACTCTTGCTAATTTATGATCCTTTTGGATTTAAGTTTGGCAAACTACAGCCTATGGGCCAGACCCAACCAACTGCTTGGTTTTGTTTGCTAGTTGCCACAGGCTAAGAATGATTTTTATATTTTTAGATGGTTGAAAAAAGAATAATATTTCATGACATTGACAATTATATGAAATTTTATTTTTAATGTCCATACATAAAATTTTATTGGAACAGACCCACATTCATTGACTTTTATATTGCCTGTGGCTGCTTTTGCATCACACTAGCAGAGTTGAGTGTCACAGAGACTGTGTGGCTTAAAAAGCCTGCAATATTTATCTGACCTTGTATAAAAAATGTTTGTCATCTACTATTCAAGACAATCATTATTTTTCTGGAAATTGTATCTGTTTTCAAGGTTATATGTAAAGTGTTAAGACAATATCCTATAAAATGCATTTTTAGGAAGTTTTGCATTACTTTCTTCCTAAGTCTTGGTAAAGTTATATAATTAGTACCTTGAAAAAAATAAAGTGAAAAGCCTTTTGGGGACTTTAGACTTTAGTGTTTAAATGTAATTATTTTTATTTGTTTTTGTTTTATTTTTTATTTTTATTTTTTTTGGCCGTGGTTATAATCTTCAG
Seq C2 exon
CATCTGCAAGAAGGACGAAAAGCTCAACAATATCTTGACATGTGCTGGAAACAGATGGATAAT
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000137942-FNBP1L:NM_001024948:4
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.056 A=NA C2=0.050
Domain overlap (PFAM):

C1:
PF0061118=FCH=PD(30.1=56.0)
A:
NA
C2:
NO


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GTTTACCTCGTGTGTAGCCTT
R:
TCCATCTGTTTCCAGCACATGT
Band lengths:
207-976
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