Special

HsaINT0035754 @ hg19

Intron Retention

Gene
ENSG00000163539 | CLASP2
Description
cytoplasmic linker associated protein 2 [Source:HGNC Symbol;Acc:17078]
Coordinates
chr3:33645646-33648250:-
Coord C1 exon
chr3:33648083-33648250
Coord A exon
chr3:33645702-33648082
Coord C2 exon
chr3:33645646-33645701
Length
2381 bp
Sequences
Splice sites
5' ss Seq
CAAGTAAGG
5' ss Score
7.66
3' ss Seq
GCATTTTTTATACTTTGCAGTCG
3' ss Score
6.89
Exon sequences
Seq C1 exon
GACATACATGGGTCTTAGAAACCACTTTCCTGGTGAAGCTGAAACATTATATAATTCCCTTGAGCCATCTTATCAGAAGAGTCTTCAAACTTACTTAAAGAGTTCTGGCAGTGTAGCATCTCTTCCACAATCAGACAGGTCCTCATCCAGCTCACAGGAAAGTCTCAA
Seq A exon
GTAAGGTCATATAAATAATGATTACTAGTCTCTTCCTCTCCTCAACTCCCTGAAGTTTCATAAGTTGGATACTTGAATATCTGTTTGCTTTCACCTAAAGCCTTGAAAGAATGGTAACTCTAATACACTTATTTATTTTGGTCTACTGTTTCAAGAGTTGGATTACTTTCCAGCATAATTCCTTCTCTTTGGATAAAGAGTTCTATGATTCATATTTTGCTTCAATATGTTCACGTCTGTAGAAGCCTGGGAAGCACTACATTTTTTTTTAATACCACAAAAACAGTACTTACAATAAATAGCCCATTTAATGGAGGAATTGTAATGGAGATTCAGAAGTTATCTTGAGAATTCTACAACACTATGTGACTAGTCTGCTTTCCTTCCTAACCTGTCGCACAGCTTAAAAATTCAGGAAATCCCTCAAGGGACAACATTATCTAGTATCTGACTTAGTTCTCTGTAACTCCATTCTCATCTTGATGACGGCTACCTCAAATCCTTACTGCTTAGCAGCCATAACCCTGTTTTCTGTCTCTCTAGCCCTATGAGATTGCTAAAATTACTGATGCCTTCTCCACTTCCTAGCACTGGCCCTGTCCCTCTTCGTGACCTCTTGCCCTGTGCCATGTATCTGCAGATTTCCCCCAGGGAAGAGCAGCTCAGAGAATGTCAGCTTAGGCCAGGCATGGTAGCTCATGCCTGTAATCCCAGCACTTTGAGAGGCTAAGGCGAGCAGATCACCTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATTAGCCAGGCATGGTGGCGGGTGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGTTTAAACCTGGGAGGTGGAGGTTGCAGTGAGCTGAGATCGTGCCACTGCACTCCAGCCTGGGAAACAGAGTGAGACTCTGTTTCCAAAAAACTTCTCTGTAATTTCTTTCTTTTTGGGATCTTGACCACCACAAAGATTGCCGGTTTCCTTGGCAACTCTGATGCAGAACTGGGACCAGGGTGAGGCAAGTGAGGCACCTAGGGTACAGAATTTAAGCAGGCACTCACTGGGTCATTCAAATACTGTACTAAAGTTCAGTTGCTTATAGGTTTTCAGAGTAAAAGCAGTTATGATCTGATTTCAAAAATAATTGTTGTAGGAATAATGACCTATCTAAACTTTTATTTAAATTTCTGTTTAAACTTCTATTTAAATTTGTGATAAGTTCCTCATCTGAAATGAGCTGTCTTTGTTGCTTTTGTTCTCTTTTTATTAACTATGCTCAGACTTTAAAGTATATACAAATCACCTGAAGATCTTTTTAAAATCTAGAATCTGATTCAGTAATTTTGGGGTGGGGCCTGAGATTTTTCATTTTTTGCAAGCTCCTAGGTGATGCTAAATGCTGTTTGTTCATGGACCATATTTTGAGTACAAAGGATCTAAAGGAAGATATTTTATATTGCTCTAATGTAACATTTTTAAACATAAACAACTTTAGATTCTGTGAACCTTAAAGTGATCCGCCTCAATCTAAGAGAATAACAATTTTGGGAGACACTTATAAAAATAATGTGATGTTAGCTTAAACATTACACGGACATTACAACCTTACAACTTAGGTGAGAGAGGCTTTGGTTATGCTGAGTTGCCTATGTGCTAGTGATAACACTACCCCTTTCTTCTAAGTAAAATATCTCAGGATACAAGTGAAAAATAATAGTACTGTTATCGAGTTCTCTTTGGTGGTCACCATGATGTGTGTTGAGGAGCAGAGTGAACAAAGGCAACCTGATCCCTGTCTCTGTAGAGCTTAGTCTTTATTCACTGCCAGTATTTTATTTTTGCTTCATAGCTAATTGAGACACATTGATACCTGATGATTGGGAGGAACTGTTCTAATGCGATTTGTAAAAGGAGAATTCAAATTGGAAGTACCAGCTAGGCACGGTGGCTCACACATATAATTCCAGCACTTTGAGAGGCTGAGGTAGGAGGATCACACTTGAGCCCAGGAGTTTGAGACCAGCCTGGGAAACTTAGGGAAACCCGATCTCTATTAAAAATTTAAAAATTAGCCACGCTTGGTGGCAGGCACATATAGTCCCAGGTAACTTGAGAGATTGAGGTGGGATGATCACTTGAGTCTGGGAAGTCAAGACTGCAGTGAGCCATGATTATGGGACTACACTGTAGCCTGGGTGACACAGCAAGACTCTGTCTCAAAAAAAAAAAAAAAGAAAAAAGAAATACTTCTCAACTTTCCACAAAATTCAGTAGTATTTTATTGGTTTTTATCAGAGGAGTGTTAAATTGTCTTCTTACTAAAAGCATTTTTTATACTTTGCAG
Seq C2 exon
TCGCCCTTTTTCTTCCAAATGGTCTACAGCAAATCCATCAACTGTGGCTGGAAGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000163539-CLASP2:NM_015097:16
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (disopred):
  C1=0.616 A=NA C2=1.000
Domain overlap (PFAM):

C1:
PF123483=CLASP_N=PD(13.3=50.9),PF123333=Ipi1_N=PD(6.5=8.8)
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