Special

HsaINT0175319 @ hg19

Intron Retention

Gene
ENSG00000188229 | TUBB2C
Description
tubulin, beta 4B class IVb [Source:HGNC Symbol;Acc:20771]
Coordinates
chr9:140135711-140136281:+
Coord C1 exon
chr9:140135711-140135869
Coord A exon
chr9:140135870-140136172
Coord C2 exon
chr9:140136173-140136281
Length
303 bp
Sequences
Splice sites
5' ss Seq
AAGGTAAGT
5' ss Score
11
3' ss Seq
CCCGCCCGCGTCCCTTGTAGTTT
3' ss Score
8.68
Exon sequences
Seq C1 exon
ATATAAGCGTTGGCGGAGCGTCGGTTGTAGCACTCTGCGCGCCCGCTCTTCTGCTGCTGTTTGTCTACTTCCTCCTGCTTCCCCGCCGCCGCCGCCGCCATCATGAGGGAAATCGTGCACTTGCAGGCCGGGCAGTGCGGCAACCAAATCGGCGCCAAG
Seq A exon
GTAAGTTGCCGGGGCGCTGGGGCCAGGCGGGCCTGCCGGGCGGTGTGGGCGGGCGGCCGGGGAAGATGGCGGCAGCAGCGGCCGGGCGGCGCCCCCGCATTGCGGCCGCCGGGCCCCCTCCGCGGGGAATTGGCCGAGCCGGGCGACCGAAGCCCCCAGGAACCCGGCGGCCAGGGCGCGCGGGGCGGGGGAGGGGCGGGGAGGGCCGGGCTGCCGCGCCCGTCCGGGGCGGGGCTGCCTCCCTGCGCACCGGCCGCGGTGACTCAGCCCCGGCCCGCCCGGGCCCGCCCGCGTCCCTTGTAG
Seq C2 exon
TTTTGGGAGGTGATCAGCGATGAGCACGGCATCGACCCCACGGGCACCTACCACGGGGACAGCGACCTGCAGCTGGAACGCATCAACGTGTACTACAATGAGGCCACCG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000188229-TUBB2C:NM_006088:1
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion (1st CDS intron)

No structure available
Features
Disorder rate (Iupred):
  C1=0.000 A=NA C2=0.135
Domain overlap (PFAM):

C1:
PF0009120=Tubulin=PU(7.2=84.2)
A:
NA
C2:
PF0009120=Tubulin=FE(16.2=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GGAGCGTCGGTTGTAGCAC
R:
CGGTGGCCTCATTGTAGTACAC
Band lengths:
254-557
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains