Special

HsaINT0037940 @ hg38

Intron Retention

Gene
ENSG00000060718 | COL11A1
Description
collagen type XI alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2186]
Coordinates
chr1:102879683-102881765:-
Coord C1 exon
chr1:102881697-102881765
Coord A exon
chr1:102879917-102881696
Coord C2 exon
chr1:102879683-102879916
Length
1780 bp
Sequences
Splice sites
5' ss Seq
CTGGTATGT
5' ss Score
8.14
3' ss Seq
TTTTATTCCTTTATTCCTAGCTT
3' ss Score
6.54
Exon sequences
Seq C1 exon
GTAAGAATTTCATCATGGCCAAAGGAGAAACCAGGAAGTTGGTTTAGTGAATTTAAGAGGGGAAAACTG
Seq A exon
GTATGTTATTACCTCAACATGAAACGATTTTTCACGAACTCAAGAAGTGACATTCTGATTATGTATTTCTGGACTTTAACAGTGAAAGTCTAAATTATGCTAAATGAGGATTCCCTGTGGTCTCTAGTTTGTTCCACTTAATATCTCTTAGACCACTGTGGTATCTTAAAGCAACCTAACATTTTTGTATAAAAGTAAATGGAAATATGCTAAATTTATGGAAAACAAGGATCAAATCATGCATACAATTTATTAAGTACCTGAGATAGACATCATAAAAATTGATTATGTTAGAAATATCAGGTATAAAGAATATAATATCTACTTAATATCTTCCTATTATTTCACTTTCTGTCTGCTTGAAACCTAATTCCTTCTTTATTCTTCATATCAATAAGTTGGAATGTGCAACTTTTTCTGATTGTTCTGGCACAAATTTAAAGATTTCCATACAATTACCAGTTCATTTCAATAATTTTCTAAAGATATTTTAAGATTAGATGTCAAAATTAAATTAATCTTTAAAAGGTGTTTAATCATATACATGTGTTTAAAGTATTTTATTTAGAAGTTATTGAATTTAAAGTGTTTTCCAGTTATCCAGATAATTATTCAGTTGTTTAATTTTCTTTGAAAAGCTATTATTTTCCATTTATGATTATTTATACAGTTATTATTTCTATACAAACTCATGCATATTAACCACTTTTATTGACACTCTCCACTGGAGTTATAATTCTCTATTACAGTCTTCAAGTTGCATATTAAATATCCATATTACATTATTATCTTTGTATAAGTTTAAAAATATATACAGATAGAACTCTATGTGTGTGGATTGAATTTTCCCAGTAGATTTTTTTCTTCAACCCCCAAGAATACTCATGATCTGACCTACTATTCAGTAAGAACTAAGTAAAATCTGTTTTAAGGAAGAAAGTAACAAATAACTGCCTTTACATTGACCTAATCTATAATCTAGGTGAACATCTTAACCTTTTTTTTTTCAAATTTAAGTGTATATGTTACAGCTGAACTCAGATATTTTTATTACCAAAAATAAGACAATTTATAAAGATGATATGAGACAGTTGCTAATAAATTACAACTGAGACTATTTTCCTGCTATAATTTCAGAATAAGTATTGACTCAACAAATATTAACTTGCCTTGTCTTGCACATTATGCCTGCTGCTGGCAATACAATGTTGAATACACACATCATCTAAAAATAGATAAACAGGCATTTCTGAAAATATTAATAACCTTTGAGGACTATAGCCCCAAAATGAAAAGTGTAGGAACATGTTTACAGATTTGGGTAAAGTTGATACATTTTGAAATGTTTGAAAGGAATAGTCAAAATCAAACAACATAAAACCAGCTAATCTTTGCATTATTCTGAGATTCCTTGGTTTTCATTGTTCCATTATTTTACCAATTTTTTTTTCAAAAAGATACAGAAATATATTGAAACATTTCTTGGAAACTAAAGCATTTTTTATAGTGTTTACTGTTTAGGAAACTAAGACTTAGAGATAAAGTGGTTTTTTCAAAGATAAGCAGTGGCTACAGTAACTTAGGTGGGATACAATTCATAAAATCTTGTCTCTGGGTCTTCTGACCCTCAATGTACACTTTTTTTCATTAGGTTAAGGTGGGTCTTTTGATTCATCTACATGCTTCTGGCATCACAGTTCACTGTCTGCAGTGATTTAATTCTTTGTAGCATAAAAGAGGAAAAGAGTCATTAGGTGTCTTTTTATTCCTTTATTCCTAG
Seq C2 exon
CTTTCATACTTAGATGTTGAAGGAAATTCCATCAATATGGTGCAAATGACATTCCTGAAACTTCTGACTGCCTCTGCTCGGCAAAATTTCACCTACCACTGTCATCAGTCAGCAGCCTGGTATGATGTGTCATCAGGAAGTTATGACAAAGCACTTCGCTTCCTGGGATCAAATGATGAGGAGATGTCCTATGACAATAATCCTTTTATCAAAACACTGTATGATGGTTGTGCG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000060718:ENST00000370096:65
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.087 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF0141013=COLFI=FE(10.4=100)
A:
NA
C2:
PF0141013=COLFI=FE(36.3=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:
GTAAGAATTTCATCATGGCCAAAGGA
R:
CGCACAACCATCATACAGTGT
Band lengths:
303-2083
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