Special

HsaINT0037932 @ hg38

Intron Retention

Gene
ENSG00000060718 | COL11A1
Description
collagen type XI alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2186]
Coordinates
chr1:102889455-102890504:-
Coord C1 exon
chr1:102890451-102890504
Coord A exon
chr1:102889563-102890450
Coord C2 exon
chr1:102889455-102889562
Length
888 bp
Sequences
Splice sites
5' ss Seq
AAGGTGAGA
5' ss Score
8.68
3' ss Seq
TTTTTCTCTGCCTTTCAAAGGGA
3' ss Score
9.3
Exon sequences
Seq C1 exon
GGACCTCCTGGCTTACCTGGTCTCAAAGGTGACCCTGGCTCCAAGGGTGAAAAG
Seq A exon
GTGAGAATAAAAGAATGTGTTATTAATAAAAGAATATGCTTTTATATACTAATAGCCCTGCTTTTGCAGATTAAAATCATTCAAAAGAAAATTTCAAACAATATCTTCATTCTAACCCTGAAAAAAGCTTCAATCCTTAGCTTCCCAGATGTATGTAGAGGGGAGAAAATATGCAAATAGTGAAAAATGTGCTGGAATTCAGTGCTATATCTTCTCAAGGTTCCATTATAGCAACCATATGTAGAAAGCATATGGTTATACTAAAATAACTATTCAGAAAATAAACAGACTGAATAACAAAATATCTATTTTTATGTTTTTAAATGTGAAAATAAAAATTTTAAACTAGAAATATCTTTCAAATACTAATTTGATGTACTAGAATTTATGCTGAGTTGCACCAAGTACTTAGAGAAATTAGCCTTTTTAAAAATGGTATTATTATTGTTTGGATTATTTTTAAATCTTCAAATGCCTTTTAAAGACTGCAGAGTCTCTGAAGAGTAGAAATTATTTCATATTAAATGAGATGCCTATTAAAATAATGAGTTTTCTGTTATTTATTCAACTTATATTATAGGAGATCATTATTGGTTTAGAGATTCCTCAAATGGAACACTTAAAATGATATTTTTAGAAAGCATTTTGTTTTGTAATATTTCCAATGCTTAATAAAGCCCTCACTTAAAGTAAGCAGTAAAAGATCCAGTTAGGTGATGAGAAGGAGATTCTTAACTGTATATTTCATTCAGAAGGGTATTTTAATGTTGTTTTATCAGCATTGTTCATTTTTATGCTTTAGAAATTTAATGTGCAAATATTTTATAACTAAAATTTTATGAAGATAGTAATGTACATGTTATTATTTTTTTTCTCTGCCTTTCAAAG
Seq C2 exon
GGACATCCTGGTTTAATTGGCCTGATTGGTCCTCCAGGAGAACAAGGGGAAAAAGGTGACCGAGGGCTCCCTGGAACTCAAGGATCTCCAGGAGCAAAAGGGGATGGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000060718:ENST00000370096:58
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=PD(2.9=11.1),PF0139113=Collagen=FE(22.4=100),PF0139113=Collagen=FE(21.5=100)
A:
NA
C2:
PF0139113=Collagen=PD(7.9=16.7),PF0139113=Collagen=FE(45.5=100),PF0139113=Collagen=PU(7.9=13.9)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
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
  • Pre-implantation embryo development