Special

HsaINT0065333 @ hg38

Intron Retention

Gene
ENSG00000137942 | FNBP1L
Description
formin binding protein 1 like [Source:HGNC Symbol;Acc:HGNC:20851]
Coordinates
chr1:93530755-93533068:+
Coord C1 exon
chr1:93530755-93530883
Coord A exon
chr1:93530884-93532921
Coord C2 exon
chr1:93532922-93533068
Length
2038 bp
Sequences
Splice sites
5' ss Seq
AAGGTAAAT
5' ss Score
8.88
3' ss Seq
AAAAAATTCTTGATTATTAGCAA
3' ss Score
1.21
Exon sequences
Seq C1 exon
GCCAAACAGCAGTTGAATCTGCGTACGCATATGGCCGATGAAAATAAAAATGAATATGCTGCACAATTACAAAACTTTAATGGAGAACAACATAAACATTTTTATGTAGTGATTCCTCAGATTTACAAG
Seq A exon
GTAAATCTTAGATATGAAGTTAATCTAGTTTTAGATTAACTGGTGTTTAAATATAAAACTTGTAAGTCTTAGACATCAGAATCTTTCTAGATTCACTAGACATCAGGGTTGGGGTGAGAGATTCCTTTATGATTATAGATTTGAAAACAAGTGTTTTCTAACTTTTAAGTCACACATTTTCCTACGTATCTACTATTAGTGTTATAAACAGTTTACTAAAACAATGACATTTGTAAGATACATTTAAATACTTTAAGTATTTTGACATGACAAAGGAGAATTAATTGAATTTGTATATTGTAATCTGCTCACCTAGAATTGAGATGTAGCATTTTTATACCAAACCAGAGTCATTGGCATCAGTCCAGATGGCAGAAATAAATCTTACAAAATATATTTGCTAGCATGGTTTTTGCCTGCTTATCATGCTGGCTCTGTTAGATGATAAATGTAATTCAGACTTTGAGCTTGCTTATAAATCCTGTCTGTCATCACTTGATGATAACAGTTGCCAAACAGCCTCAGGTAAAAAAGACCTCAGAATTTTCATGAGGGTTAAATTATTTAATTGCCTGTTCTAGAAAGAAGAGAAATTACAGAAAAGGGATTTAGTAAAGCAGTGTTGATGAGTTATTATCTCAACGAGCAGAGCTTCTGTGGGAAGAGTGTCAGCCCGGGTACACTTTTTCTTCTTTATAAGGCAAGTTGGAAATACAAAGAAAGCACAGTGAGAGATAATGAACTGGAGTGGGGACCAGAATTCTGGTCATTGAATCCAGAGGGCCAAGCCTGCCAGTCTTCACTGTGATGCTTTTCTAGGCTTAGTAGTTAAGTCTTCATATTCTGGGGAAACTATAACTTGTGGAGATAAACTACCTTTTGTGTTTTGGGCCTGATACTTGGATTTGGACCTTTCTATGGAGCAATTCTGTGAAAATGCAGGTCTCAAAGTCCCAGGCTGTGGGAGTTTGGGGAGACAAGGAGTGTAACTGCTGTCAATGAAACAGCAAGGTCAGTGCTGGCAAATAGGATATGTCAAAAAAAAAATGCCTTTAAGTTATTGGACTTTATGTGTTCCAACATATTTCCTAGTGGCATGTGCCAGTGAATTTTCAGTTGTGAGGATTCTATATGTGCCACTTTGAGCTTGTGACTTCCTGTTTTTCCTCACGTATCCCCAGCTCTGAGGTGTACACTGCAGTAGGTCTGGGTACCTGTTGATAAACAACTAGTATGGACTGTTGGTCCAGCCAAGTCTTACCAAAGTATCCTGAATTAACTTGAGGTTAGAAGTCTCAGACTTGGCCGGGGGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGTGGATCACGAGGTCAAGAGATTGAGACCATCCTGGCCAACATGGTGAAACCCCATCGCTACTAAAAATACAAAAATTAGCTGGGCATGGTGGCACGTGCCTGTAGTCCCAGCTACTTGAGAGACCGAGGCAGGAGAATTGCTTGAACCTGGGAGGTGGAGGTTGCAGTGAGCCGAGATCGCGCAACTGCACTCCATCCAGCCTGGCGACAGAGCGAGACTCCGCCTCAAAAAAAAAAAAAAAAAAAAGTCTCAGTCTTGTATATGTTATGGGCCAGTTGCTTTAAAAAAAAAAAAAAGCACCAGAATTTTGTCATCAAATGAAATGTTTTCTGGAAGCATAAACAAGAACTACTCTGATTGAATAGTAAAAGGTGGGAGTGCTATGGGGCAGGGAGCTGATAGCCAGTAAGGGGTCCTTTTAGAAGGCTAGAATCCCAGTGTCATCTGGTTTTAGGAAAACAATACTAAGTGCCTTACTATTTTTTTTCTTTCTTTTGTTGTTTAGCATGTCCCAGGTTTTAAGTATTATAAGTCAATAGCACTTGTTAAAAGGTATTAACAACAGTGTAACTATGAGGGTAGAAATATTTAATTTTTGATGGGGGATCACTAATTGAACTCCTTTAGAATGATTGAAAAATTCAGTTTTCTCTTTTTAAAAAAATTCTTGATTATTAG
Seq C2 exon
CAACTACAAGAAATGGACGAACGAAGGACTATTAAACTCAGTGAGTGTTACAGAGGATTTGCTGACTCAGAACGCAAAGTTATTCCCATCATTTCAAAATGTTTGGAAGGAATGATTCTTGCAGCAAAATCAGTTGATGAAAGAAGA
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000137942:ENST00000370253:7
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.502 A=NA C2=0.000
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:
No suggested primer sequences
R:
No suggested primer sequences
Band lengths:
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