Special

HsaINT0065334 @ hg38

Intron Retention

Gene
ENSG00000137942 | FNBP1L
Description
formin binding protein 1 like [Source:HGNC Symbol;Acc:HGNC:20851]
Coordinates
chr1:93532922-93534908:+
Coord C1 exon
chr1:93532922-93533068
Coord A exon
chr1:93533069-93534704
Coord C2 exon
chr1:93534705-93534908
Length
1636 bp
Sequences
Splice sites
5' ss Seq
AGAGTAAGT
5' ss Score
9.35
3' ss Seq
ACCTAGTTTCTTTTGTATAGGAC
3' ss Score
6.76
Exon sequences
Seq C1 exon
CAACTACAAGAAATGGACGAACGAAGGACTATTAAACTCAGTGAGTGTTACAGAGGATTTGCTGACTCAGAACGCAAAGTTATTCCCATCATTTCAAAATGTTTGGAAGGAATGATTCTTGCAGCAAAATCAGTTGATGAAAGAAGA
Seq A exon
GTAAGTGCTAAATAATTATCTTTGAATGCATCTGTTTGGTTTAGGTGTGCAGTTTAAGTTAGTGAAATGAGTTGAGAAAGGGATAAAGTAATCTGATGTGTGGTTCTAAATTATATTCTGTAGAAGAATGTCTTGCAATAGATTCCTTTGAGTTCTGAGATTCATTCTACATGCAAAAGTTCTAATTCTTTCTTAAAAAAAAAAAAAAGATTTCTAACTCTCTTCTCCCACTAAGTTTTCAGTTCTTATCAAAGAGTCTAACCTAGGAACTGTGTGTTACAAATTGTGTTATACTATTATATTAGTTTAGTGAAAATTTAGAGAAGTATGTGGTTAGAGTTGCCTTTAGCACTTGAGCTGGATCAAGAAATGTGGGTAGCATATGGAGTGATGACCAATGAGGAGGAGGAAGGAGGGCATTATGTGCAGATGAAACAGCATAGCCCTCCTCCCCTTGAGGATAGGTAATCACATTGTATCTTGATTAAGGACTAGGGTCTTTTATCTCAGTAAATGTTGATTGAGTGATCAAAAAGCATGGTTGGCAGAAACTGAGGAAAGGCAGTGGCAAGAGAAGAGAACTGGTGTTTGCAGGATATCAGATATGTGTCACATATTTTAGTCTTCATGAACCTATCAAGTAGATATTATATTAGTGAGGATCCTTTCTGTTACAGCTAATAGAATTCTCACTTAAATTTAGAAAAGAGGATTTTTGGCTTTCAGCATGGCTGGATACAAGTTTATACAATATCATTACAGCCCTCTTCTCTCTAATTACCCTTTAGCAAATTATTGCTGAGGGTAGCATTACTGACAAAAGTAAGCTATGACTTAAGGATGACTTTTGACTAAATGAAGGGCAAAATGTACTGTTAACAGAAATAGGCAACAAAAGAGAGGTTGTTGTTAGGGGTGGGGAGGAATTTGTAGAGATACTCTGAAAATAATGAGTTTAAGGTATCACTAAAGCATTCAGGTAGAGGTATGTATGTCTAAAAACAATATTTATGTGAGTTTAAAAATTTTAAATACATGGTATTAAACTTTCAAATGTTGTTTGCACTCAGTAGTGTTTATGAGATCTTTTCCCTGTTGCTCTGTTAACATTCCACAGTATATATTTAATTTATTTATCTTTTCCCATGTTGGATGAGTTAGAAAGCCTTTCCTACTCATCTTTTACTCTCTTTTACAATTAGATGTTCTTTCCTCATTCCAAAGATTAGCTTCTTTGTTGACATCTATCTTTTAAAGCAAAAAGCCTTTTTCCTTTGAAACTTCTCAGAATTTCTACTTGTTAATAACCTCTTTCTGTATTCTTTTTGTCAGTTAGGTCTTTTTCAGCTAAGTAGTCTTCAGATGAATTTCAGGTGGTTAAAGCTACCAAGTAAAAACATTTTATGAATATTATAAATTAATTAAGTTGTAATTTGCAAGTATATTTTTCTTTTGGGATTAAAATACTTTGAGTTTGTTACACATTCATGGGAATAAATTATTTACCTTAATGATTATTGTGGAATTATTTATTTAAACTTATATTTGTTGTTTTTTTGTACTGAAAAAGTTATGAAAGCTGATGTAGAATTATGAGCAAGTGAAACAGTTTTAAAACCTAGTTTCTTTTGTATAG
Seq C2 exon
GACTCTCAAATGGTGGTAGACTCCTTCAAATCTGGTTTTGAACCTCCAGGAGACTTTCCATTTGAAGATTACAGTCAACATATATATAGAACCATTTCTGATGGGACTATCAGTGCATCCAAACAGGAGAGTGGGAAGATGGATGCCAAAACCACAGTAGGAAAGGCCAAGGGCAAATTGTGGCTCTTTGGAAAGAAGCCAAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000137942:ENST00000370253:8
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=0.279
Domain overlap (PFAM):

C1:
NO
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:
ACAAGAAATGGACGAACGAAGGA
R:
GGCTTCTTTCCAAAGAGCCAC
Band lengths:
342-1978
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