Special

HsaINT1008102 @ hg38

Intron Retention

Gene
ENSG00000204248 | COL11A2
Description
collagen type XI alpha 2 chain [Source:HGNC Symbol;Acc:HGNC:2187]
Coordinates
chr6:33165549-33165984:-
Coord C1 exon
chr6:33165931-33165984
Coord A exon
chr6:33165817-33165930
Coord C2 exon
chr6:33165549-33165816
Length
114 bp
Sequences
Splice sites
5' ss Seq
CCGGTGAGT
5' ss Score
10.9
3' ss Seq
CCATCTGTCCCTGCACCCAGGGT
3' ss Score
8.95
Exon sequences
Seq C1 exon
GGCCCAGGCGGACCCAAGGGAGAGAAGGGTGTGCAGGGCCCTCCAGGACACCCG
Seq A exon
GTGAGTGAGGAGTCAGGGCTGCTCCCAGGGCCGTACCCCTCTGCTCCACTGCTGCCACACTTCACCCTCACACCAACCTTGTCTCTTGCCCTCTCCATCTGTCCCTGCACCCAG
Seq C2 exon
GGTCCCCCAGGCGAGGTGATCCAGCCACTGCCCATTCAGATGCCCAAGAAGACTCGGCGCTCGGTGGATGGAAGCCGTCTGATGCAGGAAGATGAGGCCATACCGACCGGGGGAGCCCCCGGCAGTCCTGGGGGGCTGGAGGAGATCTTTGGCTCACTCGACTCCCTGCGGGAGGAGATCGAGCAGATGAGGCGGCCAACAGGGACCCAGGACAGCCCTGCTCGCACCTGCCAGGACCTGAAGCTGTGCCACCCAGAGCTTCCCGATG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000204248:ENST00000374708:60
Average complexity
IR
Mappability confidence:
NA
Protein Impact

Alternative protein isoforms

No structure available
Features
Disorder rate (Iupred):
  C1=1.000 A=NA C2=0.933
Domain overlap (PFAM):

C1:
PF0139113=Collagen=FE(27.0=100)
A:
NA
C2:
PF0139113=Collagen=PD(12.7=8.9),PF0141013=COLFI=PU(41.5=30.0)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Primers PCR
Suggestions for RT-PCR validation
F:
AAGGGAGAGAAGGGTGTGCAG
R:
CTGTCCTGGGTCCCTGTTGG
Band lengths:
254-368
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains