Special

HsaEX6008779 @ hg38

Exon Skipping

Gene
ENSG00000164659 | KIAA1324L
Description
KIAA1324 like [Source:HGNC Symbol;Acc:HGNC:21945]
Coordinates
chr7:86925528-86938214:-
Coord C1 exon
chr7:86938126-86938214
Coord A exon
chr7:86926736-86926916
Coord C2 exon
chr7:86925528-86925656
Length
181 bp
Sequences
Splice sites
3' ss Seq
TTTTTTTTTTTTTTTTGTAGACA
3' ss Score
10.48
5' ss Seq
AAGGTAGGA
5' ss Score
9.45
Exon sequences
Seq C1 exon
AGGAAGGATCCAGTGAGTGTACAGAGCGCCCTCCCTGTACCACAAAAGACTATTTCCAGATCCATACTCCATGTGATGAAGAAGGAAAG
Seq A exon
ACACAGATAATGTACAAGTGGATAGAGCCCAAAATCTGCCGGGAGGATCTCACAGATGCTATTAGATTGCCCCCTTCTGGAGAGAAGAAGGATTGTCCGCCTTGCAACCCTGGATTTTATAACAATGGATCATCTTCTTGCCATCCCTGTCCTCCTGGAACATTTTCAGATGGAACCAAAG
Seq C2 exon
AATGTAGACCATGTCCAGCAGGAACGGAGCCTGCACTTGGCTTTGAATATAAATGGTGGAATGTCCTTCCTGGCAACATGAAAACTTCCTGCTTCAATGTTGGGAATTCAAAGTGCGATGGAATGAATG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000164659-'18-19,'18-18,23-19=AN
Average complexity
A_S
Mappability confidence:
100%=100=100%
Protein Impact

ORF disruption upon sequence exclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.000 A=0.016 C2=0.000
Domain overlap (PFAM):

C1:
NO
A:
PF076998=GCC2_GCC3=PU(67.6=37.7)
C2:
PF076998=GCC2_GCC3=PD(29.4=22.7)


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Inclusion Isoforms:


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GGAAGGATCCAGTGAGTGTACA
R:
TCCATCGCACTTTGAATTCCCA
Band lengths:
210-391
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains