Special

HsaINT0002216 @ hg19

Intron Retention

Gene
Description
aggrecan [Source:HGNC Symbol;Acc:319]
Coordinates
chr15:89414613-89415316:+
Coord C1 exon
chr15:89414613-89414771
Coord A exon
chr15:89414772-89415233
Coord C2 exon
chr15:89415234-89415316
Length
462 bp
Sequences
Splice sites
5' ss Seq
ACAGTGAGT
5' ss Score
8.34
3' ss Seq
CACCCTCACCCTTTCCCCAGACA
3' ss Score
10.32
Exon sequences
Seq C1 exon
ACCAGGAGGTATGTGAGGAGGGCTGGAACAAGTACCAGGGCCACTGTTACCGCCACTTCCCGGACCGCGAGACCTGGGTGGATGCTGAGCGCCGGTGTCGGGAGCAGCAGTCACACCTGAGCAGCATCGTCACCCCCGAGGAGCAGGAGTTTGTCAACA
Seq A exon
GTGAGTGCGGCGGGGCCTCTGGAGCCTGAGAGGAGAGTGGCGGTGTAGGCAAAGGGCCTCACCTTTCAGAAGGCAGCAGATTTGGGCCTCGTGAGACTGCAGGACAGGGACCTGGGGGAGGGGGAACAGTGTTCCCACAGTCTGAGCTCCCAGAGAGAAGACAACGGTCTTTGGGGCCAGAAGCTGTGGCTGCAGCCAGGGCAGACCCATTGCCAGCCAGAGTCAGCCCAAGACTAAGCTATGGCTGTCACCCGTCCATGCCAGCTTGGAGAGGTGGCCCGAAGTGCACTCCAGGCATGCACGTGCTGAGCCTCTTGTGAGGACCTGAGAAGCACGTGCCTTGCTCCTAGGAGCCCACCCACCTCCTTTCCTCCTCCATCCCCTCTGCCTCCGTGAGCTCAAGTTTCTCAGACACCCTCAGGGTGTCCAGTGTGATGCCTGACACCCTCACCCTTTCCCCAG
Seq C2 exon
ACAATGCCCAAGACTACCAGTGGATCGGCCTGAACGACAGGACCATCGAAGGGGACTTCCGCTGGTCAGATGGACACCCCATG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000157766-ACAN:NM_013227:14
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.244 A=NA C2=0.079
Domain overlap (PFAM):

C1:
PF0005916=Lectin_C=PU(30.2=59.3)
A:
NA
C2:
PF0005916=Lectin_C=FE(25.5=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
CCAGGAGGTATGTGAGGAGGG
R:
TGGGGTGTCCATCTGACCAG
Band lengths:
239-701
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