Special

HsaINT0037927 @ hg38

Intron Retention

Gene
ENSG00000060718 | COL11A1
Description
collagen type XI alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2186]
Coordinates
chr1:102912159-102913690:-
Coord C1 exon
chr1:102913637-102913690
Coord A exon
chr1:102912213-102913636
Coord C2 exon
chr1:102912159-102912212
Length
1424 bp
Sequences
Splice sites
5' ss Seq
CCGGTGAGT
5' ss Score
10.9
3' ss Seq
TATTTTTTCACATTTTATAGGGT
3' ss Score
8.49
Exon sequences
Seq C1 exon
GGTCAAGATGGTGTTGGTGGTGACAAGGGTGAAGATGGAGATCCTGGTCAACCG
Seq A exon
GTGAGTAAATGCACTAATTTATTTTTAAGTTTTTACATAGTCTCAAGGCATTTTAATGAGATAATTAGAAGTAATCAGCCTTTGAAAAACATAGCTCTATGTATATGCACTTTTTTGAAAGAATTATCAAAAAAATTTTTGAATTCCCATTAAAAATCAATCTTACATGGAGTGTTTCTTATTTGATGTAAATTAATAAACAGTATTTATAATGAAAAGTGTAATCATATTATACTAATAAGGTTGTCACAATATATCAAATTCAGTTATCTATCCATTGTGTTAAAAAATTAAAATCACTAATAATACTAAAAGCAAAGTTATTTCCTATCATTAGCAAAAGTTATTATCCCATCATTAGCATGAATTATATTAATTGTGAACCTAAATGAACTCTCAACATAGTATAGGCCTTTTTAAAAAAAACTTGTGAATGATACAGGAGTGTACTTTGACCACATTTAGTTATTTAGGGAGAAAGTAAGGGAGGGAACTCACTTTAGGAGCCAAAGACAATGGTCCCTCAACACAATTTTGTCTCTGGGGCCATTCCCACTAGATGCTTTGCTATCACAGATACAGGCTTATTCTGCATAGACAGACCTGTGGATCATATCTCAGCATGTGTATTAGTCCATTCTCATACTGCTGTGAGGTACACAAGAATGGGTAATTTATAATGGAAAGAGGTTTAATTGACTCACAATTCTGCATGGCTGGGAAGGCCTCAGGAAACTTACAATATGGTGGAAGGCGAAGCAAGCATGTCTTTCTTCACATGGCAGTAGGAGAGAGGAGTGCAAAGTGAAGGGTGAAAAGCCACTTATTAAACCATCAGATCTCGTGAGAACTCACTCACTATCACAAGAACAGAATGTGAGTAACCACCCCCATCACTCAATTACCTCCCACTGGGTCCCTCTCAGGATACATGGGGATTATAGGAACTACAATTCAAGATGAGATTTGGGTAGGGACACAGCCAAACCATATCAGTATGTTATATACAACTTGGCATAGAATGTTAGTGTTGTACAAAAATAAATTTAAAAGTAATAGTATTATGTTTTCACATATTTATGTGATATGAGCAGAATTATTAACCATATGATTATATTAATTAGCATGCCTGTTTAATGCTTGCCAGATATAAATTAGCACTTTTTAATAGGACACAGTTTTAAATAAAGAGAATTTGATTCACTTTGTTCTAACTATAAATAATTTTACCATCTAAATTTACCAGCTCTAACTATAAATATCTAGAGGAAGTTTAGGTATCTGAAATAGGGCTGAGATTTTCCAGGAAATATTGACATGTGGAAATGAAGAAAGAGGGTTGGTTTCCATCCAGATTTTGAAAATTTATGTGGGCCACAAAATAATATCCAATTTTGTTAAAGGTATTTTTTCACATTTTATAG
Seq C2 exon
GGTCCTCCTGGCCCATCTGGTGAGGCTGGCCCACCAGGTCCTCCTGGAAAACGA
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000060718:ENST00000370096:53
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(29.3=100)
A:
NA
C2:
PF0139113=Collagen=FE(23.0=100)


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