Special

HsaINT1008077 @ hg38

Intron Retention

Gene
ENSG00000204248 | COL11A2
Description
collagen type XI alpha 2 chain [Source:HGNC Symbol;Acc:HGNC:2187]
Coordinates
chr6:33172050-33172378:-
Coord C1 exon
chr6:33172289-33172378
Coord A exon
chr6:33172104-33172288
Coord C2 exon
chr6:33172050-33172103
Length
185 bp
Sequences
Splice sites
5' ss Seq
GCTGTGAGT
5' ss Score
7.39
3' ss Seq
CCCAAATGTCTGGTTCATAGGGT
3' ss Score
6.16
Exon sequences
Seq C1 exon
GGTGACCCTGGTCCCCCTGGGGCCCCAGGGAAGGATGGTCCTGCTGGTCTGAGGGGATTCCCAGGAGAGAGAGGCCTCCCAGGCACTGCT
Seq A exon
GTGAGTGTGACTCCCAGACCCCTGCCTGTCACAAGCACCAAGCATCCTGAGTCCCCACCCCGACCCTGTCCCTGACCCCCTCCATGTCACTCCCCACTTCCATCTTTTGGAGCCTGTCTTCCCTCTCCAGCTCTCACCCTTCTCTTTTCGTGAAGTCTCATCTTCCCCAAATGTCTGGTTCATAG
Seq C2 exon
GGTGGACCTGGTTTGAAGGGGAATGAAGGTCCGTCTGGCCCCCCTGGCCCTGCA
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000204248:ENST00000374708:38
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(35.8=100),PF0139113=Collagen=PU(43.9=96.7)
A:
NA
C2:
PF0139113=Collagen=PD(13.6=61.1),PF0139113=Collagen=FE(25.8=100),PF0139113=Collagen=PU(25.8=94.4)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Primers PCR
Suggestions for RT-PCR validation
F:
GGTGACCCTGGTCCCCCT
R:
GGCCAGACGGACCTTCATTC
Band lengths:
130-315
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains