Special

HsaEX6010286 @ hg38

Exon Skipping

Gene
Description
paired box 4 [Source:HGNC Symbol;Acc:HGNC:8618]
Coordinates
chr7:127613022-127613881:-
Coord C1 exon
chr7:127613756-127613881
Coord A exon
chr7:127613450-127613532
Coord C2 exon
chr7:127613022-127613091
Length
83 bp
Sequences
Splice sites
3' ss Seq
GTGAGACTCGATCTCCGCAGAGT
3' ss Score
5.77
5' ss Seq
AGGGTGAGT
5' ss Score
9.25
Exon sequences
Seq C1 exon
CTGTTTTGGCTCCAGCTGTCCTCACTCCCCATAGTGGCTCTGAGACTCCCCGGGGTACCCACCCAGGGACCGGCCACCGGAATCGGACTATCTTCTCCCCAAGCCAAGCAGAGGCACTGGAGAAAG
Seq A exon
AGTTCCAGCGTGGGCAGTATCCTGATTCAGTGGCCCGTGGAAAGCTGGCTACTGCCACCTCTCTGCCTGAGGACACGGTGAGG
Seq C2 exon
GTCTGGTTTTCCAACAGAAGAGCCAAATGGCGTCGGCAAGAGAAGCTCAAGTGGGAAATGCAGCTGCCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000106331-'6-11,'6-10,7-11=AN
Average complexity
A_S
Mappability confidence:
100%=100=100%
Protein Impact

ORF disruption upon sequence exclusion

No structure available
Features
Disorder rate (disopred):
  C1=0.922 A=0.613 C2=0.701
Domain overlap (PFAM):

C1:
PF0004624=Homeobox=PU(29.8=39.5)
A:
PF0004624=Homeobox=FE(47.4=100)
C2:
PF0004624=Homeobox=PD(19.3=45.8)


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GCTGTCCTCACTCCCCATAGT
R:
CCCACTTGAGCTTCTCTTGCC
Band lengths:
167-250
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains