Special

HsaEX0004110 @ hg19

Exon Skipping

Gene
Description
ankyrin 1, erythrocytic [Source:HGNC Symbol;Acc:492]
Coordinates
chr8:41591489-41754280:-
Coord C1 exon
chr8:41753873-41754280
Coord A exon
chr8:41615554-41615655
Coord C2 exon
chr8:41591489-41591587
Length
102 bp
Sequences
Splice sites
3' ss Seq
CCTGTTGTTTTTCCTCACAGGCC
3' ss Score
11.79
5' ss Seq
CAGGTAAGT
5' ss Score
10.86
Exon sequences
Seq C1 exon
GGGAGGCGGCGGGCCCTGCCCAGAGCCCGTCCCGGGCGCCGGCAAGCGAGCTCCGGCCGCGGCGGCAGCGCCATCCCGGGCCGCGGGCAGCCGCCCCTCGCCCTCCGCGTCCGGAACTGCCTTCGCCTTCCCGCGACCCCGCAGCAGCCGGCCCTCGGGGCGCCACGAACGCTGTCCCCTCTGTGGAGCAGAGACCCCCTTCCCCTTCTTAGGGGGTGTCGCCTCGGGGATCGCTGAGCGCTAGGGGTCCAGGAGGCGGGGACGGGAGCGCCGTGACCCGCCATGGCTCAAGCGGCCAAACAGCTGAAGAAAATCAAAGACATCGAGGCGCAGGCCCTCCAGGAGCAGAAGGAGAAGGAGGAATCCAACAGGAAGCGGAGAAACCGCTCCCGTGACCGAAAGAAGAAG
Seq A exon
GCCGATGCTGCTACCAGCTTTCTGAGAGCAGCAAGATCAGGTAACTTGGACAAAGCTTTGGATCACCTGCGGAATGGGGTAGATATTAACACCTGTAACCAG
Seq C2 exon
AATGGGTTGAATGGCTTGCATCTGGCTTCTAAGGAAGGCCATGTGAAAATGGTGGTTGAACTTCTGCACAAAGAAATCATTCTAGAAACGACAACCAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000029534-'0-4,'0-3,3-4
Average complexity
C2
Mappability confidence:
100%=100=100%
Protein Impact

Alternative protein isoforms (Ref)

No structure available
Features
Disorder rate (Iupred):
  C1=0.762 A=0.048 C2=0.017
Domain overlap (PFAM):

C1:
NO
A:
PF127962=Ank_2=PU(29.0=79.4)
C2:
PF127962=Ank_2=FE(34.4=100)


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
GACCCCCTTCCCCTTCTTAGG
R:
AGCCAGATGCAAGCCATTCAA
Band lengths:
243-345
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