Special

HsaINT1008065 @ hg38

Intron Retention

Gene
ENSG00000204248 | COL11A2
Description
collagen type XI alpha 2 chain [Source:HGNC Symbol;Acc:HGNC:2187]
Coordinates
chr6:33175574-33176069:-
Coord C1 exon
chr6:33176016-33176069
Coord A exon
chr6:33175682-33176015
Coord C2 exon
chr6:33175574-33175681
Length
334 bp
Sequences
Splice sites
5' ss Seq
AGGGTGAGT
5' ss Score
9.25
3' ss Seq
TGTCCTTCCCTCTCACACAGGGC
3' ss Score
11.36
Exon sequences
Seq C1 exon
GGTGAGGATGGCTTTCCTGGGTTCAAAGGTGACATAGGCGTGAAAGGTGACAGG
Seq A exon
GTGAGTAGAGACCCCACACTGGCCCCAATTCCGTGTTCTACTGAGCCTCCACTCTGGAGACGCCAAGCACCGGTTTATTCTCCTGAGTCTCCAGACTCCACAGTTCCAGTGCTGTGTTCCCTTGGGAGCCTGACCCCTACAGGATGATAGCCCCATGGTCTGTGTCATGCCTGCCCTCCCATCACTACACTATCCCTACCCTGTGGGCTTCCTGTCCTGCAGTGGCTCCTGGGACCCCTCTAGCCCTCCTCAGCCTCACTGTTGCCCATTTCTCCTCTGGGCCCAGAGCCCACCTCCAGTCCCCAGCACTCACCTGTCCTTCCCTCTCACACAG
Seq C2 exon
GGCGAAGTTGGAGTCCCTGGTTCCAGGGGAGAGGATGGTCCTGAGGGGCCAAAGGGACGCACTGGACCGACTGGAGACCCTGGGCCCCCAGGGCTCATGGGCGAGAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000204248:ENST00000374708:27
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

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

C1:
PF0139113=Collagen=FE(26.6=100)
A:
NA
C2:
PF0139113=Collagen=PD(7.1=16.7)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
No suggested primer sequences
R:
No suggested primer sequences
Band lengths:
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains