Special

HsaINT0037890 @ hg38

Intron Retention

Gene
ENSG00000060718 | COL11A1
Description
collagen type XI alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2186]
Coordinates
chr1:103003215-103004488:-
Coord C1 exon
chr1:103004444-103004488
Coord A exon
chr1:103003269-103004443
Coord C2 exon
chr1:103003215-103003268
Length
1175 bp
Sequences
Splice sites
5' ss Seq
GCTGTAAGC
5' ss Score
4.47
3' ss Seq
GCTTTTTCTTTTTCTCCTAGGGC
3' ss Score
10.71
Exon sequences
Seq C1 exon
GGAGAAGATGGAGAAATTGGACCAAGAGGTCTTCCAGGTGAAGCT
Seq A exon
GTAAGCAACTTACTTTTTATTTTTAAGTAATATTTCTAGTTTTTAGGACTAGTGACTGGTGTTACACATATAAAAACAATGATAAACCCAGGTAAACATTGCAGTCTTAGCTAAGCTAACCAGATAATTGCCATGCGAAAAAAATTAAAAAGGATATATAGAGCTCCTTTTGTTACAGAGAAAATCTTAGACAATTGAGGGAAAAATCTGTGGAATGTAACATTTCCAGCCAAAAAAGTTACCTTACCTAGTTTTTGTTGCTGTTTCTTTGTTTTGTTTTTTGTGCTGTCATCAATAGCTCCGAAATTTATGTACTGAGAAGAAATGAATCCTATTACCAGAAGAAAAAAAATAATATGTCACTTGGAATATACCAGACATATGGAATATATCACTTTTCTCCACCAAATATTACAAATGAGGAAACTGATCTGGGAAGGTTTACTTGAAGCTAGCTAACAAAATAACTAAACTGGAAATAGGCCTCCTAATTTTGGTTTTAAATTGCTGCATTCTACCTTGCGCCACATTTTAGATCCTTGTCAAGTAAGTTCAAGCAAATGGGAGAGAAATTAGATTATTTTATTGGCTTTTCTAAAGAAGGAAAAGAAGGTGAGCAGGTGCAGGAGGGGGAAAAAGAAGAGAAGGAGAAATCAAGTGTGAATAATAATAATTTAAGAAACCTCGAAAAATGGTTTCTGTAATCTGCATATATAGTTACACAGATGATCGTTTTCTTTCCTCAGTGAATGCTGTCTTAAGATGAAATTTACCTAAATGTACAATAAATGAGAATCAAGACTCTTCTATTTATGTAGTATATCTGATTGAATAATAATGTTCGATGCTGTCACTGAAATCAAAAAATGACACAAAAGTGTCTTATAGAAAATATTAAACTGTTTCCTATTTTAAAAATTCCCCAAGTGATTCATATGTAATATTATAGAATCAAAGAAACACAGTTTCTGTACTAAAAACTGTTATTTATTCTGGCTTTTGGATCAGTATAAACACTAGATATTTATGTTATGGACATCACTTTCAGTGTGTTAATAAAAGATGTCCAAATATTTTTATTCTAAAAATAACCTTAGGATTTCTTCATTGAAAGAGGCATGTTATTAGGACATTTTTTTTTTTTAATAAAGGCGTGCTTTTTCTTTTTCTCCTAG
Seq C2 exon
GGCCCACGAGGTTTGCTGGGTCCAAGGGGAACTCCAGGAGCTCCAGGGCAGCCT
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000060718:ENST00000370096:20
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(15.4=66.7),PF0139113=Collagen=FE(19.4=100),PF0139113=Collagen=PU(17.2=73.3)
A:
NA
C2:
PF0139113=Collagen=FE(23.6=100),PF0139113=Collagen=FE(26.6=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
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