Special

HsaINT0065333 @ hg19

Intron Retention

Gene
ENSG00000137942 | FNBP1L
Description
formin binding protein 1-like [Source:HGNC Symbol;Acc:20851]
Coordinates
chr1:93996312-93998625:+
Coord C1 exon
chr1:93996312-93996440
Coord A exon
chr1:93996441-93998478
Coord C2 exon
chr1:93998479-93998625
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-FNBP1L:NM_001024948:7
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.512 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