Special

HsaEX0016520 @ hg19

Exon Skipping

Gene
ENSG00000139219 | COL2A1
Description
collagen, type II, alpha 1 [Source:HGNC Symbol;Acc:2200]
Coordinates
chr12:48366719-48371436:-
Coord C1 exon
chr12:48371383-48371436
Coord A exon
chr12:48371103-48371210
Coord C2 exon
chr12:48366719-48366940
Length
108 bp
Sequences
Splice sites
3' ss Seq
TGAGACCTCTCTCCTGACAGGGT
3' ss Score
8.92
5' ss Seq
GCTGTAAGT
5' ss Score
8.56
Exon sequences
Seq C1 exon
GGAAGCCCCGGTGCTGATGGCCCCCCTGGCAGAGATGGCGCTGCTGGAGTCAAG
Seq A exon
GGTGATCGTGGTGAGACTGGTGCTGTGGGAGCTCCTGGAGCCCCTGGGCCCCCTGGCTCCCCTGGCCCCGCTGGTCCAACTGGCAAGCAAGGAGACAGAGGAGAAGCT
Seq C2 exon
GCAGGAAACTAACTGGTGTGAGTCAAATGCCCCCTGAGTGACTGCCCCCAGCCCAGGCCAGAAGACCTCCCTTCAGGTGCCGGGCGCAGGAACTGTGTGTGTCCTACACAATGGTGCTATTCTGTGTCAAACACCTCTGTATTTTTTAAAACATCAATTGATATTAAAAATGAAAAGATTATTGGAAAGTACATATTGACTTGTGGTTTGTTCTTTAGTTTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000139219_MULTIEX1-39/47=38-C2
Average complexity
C2*
Mappability confidence:
100%=100=100%
Protein Impact

Alternative protein isoforms (Ref)

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

C1:
PF0139113=Collagen=FE(19.5=100),PF0139113=Collagen=PU(16.5=77.8)
A:
PF0139113=Collagen=PD(16.1=38.9),PF0139113=Collagen=FE(41.2=100)
C2:
NA


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:
AGAGATGGCGCTGCTGGA
R:
ACTAAAGAACAAACCACAAGTCAA
Band lengths:
243-351
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