Special

HsaINT0062495 @ hg38

Intron Retention

Gene
Description
fibrillin 2 [Source:HGNC Symbol;Acc:HGNC:3604]
Coordinates
chr5:128271999-128273968:-
Coord C1 exon
chr5:128273840-128273968
Coord A exon
chr5:128272119-128273839
Coord C2 exon
chr5:128271999-128272118
Length
1721 bp
Sequences
Splice sites
5' ss Seq
AAGGTTAGT
5' ss Score
8.54
3' ss Seq
TGCCGGGCTTGTTTTTGCAGATG
3' ss Score
10.09
Exon sequences
Seq C1 exon
ACAACAACGAATGTGGGTCTCAACCTTCGCTTTGTGGAGCAAAGGGAATCTGTCAAAACACTCCAGGCAGTTTCAGCTGTGAATGCCAAAGAGGGTTCTCTCTTGATGCCACCGGACTGAACTGTGAAG
Seq A exon
GTTAGTTGATTTGCTCAAAAATTCTTAATCTAATAACAGTAAACCATATATATTTTTAACTTCCAAGACAAATTGGTATAATCTGAAAAAAAGAAAAAAAAGTATTGAACAAAATAGGACCCAGCAACTTATTCCTGGTCATAAATTTCTATGTATCACTTTGGGGACAGAGGGAAACCTAAATGCAGTGAAACAAAAATTCTGTGATTACGAATTGACTTTTAAAGTAACTGTTGACTAATCATGGATCTGAGAAAGAATTGAATTGAAAAAGAATTCTGTGCCTAATATGGTTTGCGGTAGTGTACAAGCATACCAGAAAAAAATAATAATTGGCCTTTTGTTCCATGATTCTTAAATGTATAAGAATTAAATATAAAAAGAATCTGTCATCAGAGAGAATTGAACAAATGTACTGAACACGCTAAGGTGAAATGATGGCTGTTTCTGTTTTTTACGAGTCAAGCTCCCGCTTCACTCCTTCACTTTCTTACAGTGGACCTTGGTCTCCTCTGCAATAACTATTTCCTGTAAAATCCAAGGGAACATTTAAGTGGAAACAAAATAAGAACATGCTTGCAGTTAAGAAAATTTCATCTAGTTCTTCACTATTTATATTGCAAGTGGCAGTGTATGACAAGAAAAATGTATTAGGATTAGTGTCTTATAAACACCCATGCCAGAGATTATGAGACTATATTTATTTCCCTTACATTCTTATATCGTATTGCAATTTATAGTTTTCTTGATTTTAATCACCCTTTTAACATTAACTATTCTTAGAAATATATGATTTGGATTTCTAGAAATATATGTTAAGTATTTAATTTGCTCTCTGTAAGGCTTGTGGGGCTTTTATATGTATCTCATTTTCAGCAAAGAAAAATTCAGTTTTTAAAATGTCAATTTTAATATTTTATCTTTCAAATCGTTGAGACGTTGAAAGTATTCTTAACCTACAGCTGTTTGCCACATGCGAGTTCAGCTCGTGACCATCCCCATAAGATACCATTTATTAATTATCCATGTAAATTTGTTACACCCCTCAGACATGCCAATTTTATTTTACTCTTTATGGATAGATTTCAAATATTCGGTTGTCATTCCAAAAAAGCATACATAAATAAAGAAATTATTCCACATGTATAATAATACCACATCTTGTCTAAAAATAACATATTTAAATACTTAAGAGGGATTTGCATCTAATTAATCTTGAATGGTAATAAAAATTTTTACGTGCAATATAATTGTACTTTTTAGGTATCTCTGTAATGCTTCTATCCTCCCAAAAATGAGGATTGTATCTCAGTCACTTTCAAACTTACTGGACTATGCAATGCAAATATATTTTATATATATATATATATATATATGATTTACCAAATAAATCATACCATTTGCAGTTAATTAGTTCAAAATGTACAACATTTGTGGTTGCTATGGTTGACTTGCTGAAATTGAGATGTTATTTAGAGCACTGACATGCCGTGGTCTGGTGGAGAGCAGAAGAATGAGCTGGTCTCTTATCTCAGAACTGTTCCCTGCACCACCACTGACTAATAACCATGTGACCTGGAAAAATGACAGCCTCTCTATGTGTCATGTCTTGTTTGTTTGTTTGTTCCCATGATAACAGTTACCCCAGGTTTCGTTTGGAGTGCATTTAAAAATAGTAGAAGAAAGGTGACATAAAGGTTTTGCCGGGCTTGTTTTTGCAG
Seq C2 exon
ATGTTGATGAATGTGATGGGAACCACAGGTGCCAACACGGCTGCCAGAACATCCTGGGTGGCTACAGATGTGGCTGCCCCCAAGGCTACATCCAGCACTACCAGTGGAATCAGTGTGTCG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000138829:ENST00000508053:67
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=0.000
Domain overlap (PFAM):

C1:
PF0764510=EGF_CA=WD(100=95.5),PF0764510=EGF_CA=PU(0.1=0.0)
A:
NA
C2:
PF0764510=EGF_CA=WD(100=95.1),PF0764510=EGF_CA=PU(0.1=0.0)


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:
ACAACGAATGTGGGTCTCAACC
R:
CGACACACTGATTCCACTGGT
Band lengths:
246-1967
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