Special

HsaINT0037900 @ hg38

Intron Retention

Gene
ENSG00000060718 | COL11A1
Description
collagen type XI alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2186]
Coordinates
chr1:102987633-102989571:-
Coord C1 exon
chr1:102989518-102989571
Coord A exon
chr1:102987741-102989517
Coord C2 exon
chr1:102987633-102987740
Length
1777 bp
Sequences
Splice sites
5' ss Seq
AGAGTAAGT
5' ss Score
9.35
3' ss Seq
GTTGTTATTCTGTGCCTCAGGGA
3' ss Score
6.94
Exon sequences
Seq C1 exon
GGTGAAGATGGTTTTCCAGGATTCAAAGGTGACATGGGTCTAAAAGGTGACAGA
Seq A exon
GTAAGTATAGAGAAAATGTACACCAGTACACAAAATTTAATATATATATATATTTTTTCCTTTGCTTATCTTTAAATATAGTAAGCATATGATAAATAAAATGTTTGTACTACCTAAGTCTTTACTCATTTAAGTTTTTATACAAAGATTTAAGGATTTTAATTTTTGTGGAGATAGTGTAGTATCAATTGTCTTTTAGATGTTATATTTCCATAGGTTCCATAATAAACATGAGCATGCACGCGTGCACACACACACACACACATGCACACACACGTGTTAGTATTTATACACAGGACATTAGAAAGTTAGATCAAATTACTAGAAGTAATTTGATAAGTTTGCTCTAAATTTTGTTCATATATAATGAGCTATGCTGCCTGGAAAGTATACGTCTGTAACTTTCATGAATTTTCATTATATGGTGGTGTTCAATTTTTGAATGTAAAAATAGTAGTTTTTTCTAGTAATACATTATAGAAAACAAACAGAAATATTAGTTATCTAAAGCAAATTAAATGCTTTATTGGGAAGATTTATTTTTAAGTAATATACTAGTACCTAATACATCTGAATAAAGAAGCATTCTATAGAAAATATTTCTTTTCCTAAAATTCAAATGAAGTCTGCATGCAGGATTGGGGGCAATAACATCCATATACAAGTTCTTAAACGTTAAAGATAAAAGCCACGTACAAAAGAGAGACATTTTTCTTGTGTTCCAAACAGTAATTTCCAAAGCTGCTGAACAATCTTTATTATTATTTTTCCCTCTCTCTATAACACAGGTGCATTAAAAGCAATTTAATGTCATATATGATATGATTCAGCTTTTGTAGATTTTCAAATATCAGACTATATTCAGTTGTTTATTAAATATGAAAAGATTGATTAAGTCAAACACTTTCAAGCCTCTTTTTCATGAACAAAAACATGAGTAAACACACCAAAGTTGAAAACTCTGACTTTCAACAGACTGTAATTTATGCCTTTCAATCTCCAAATATATTTTTGTAACTGCCTGATGGGTTTATCTTGCCTGCTGCCCAGACAGGGCCTATTTATCCAGACAGGGGAATTGCAAACTCTTTCTCTATGCATACAGTTAGCTGAATAGGAGACTAGAGTTTTATTATTACTCAAATTAGCCTCCACAAAAATTTGGAGGATAGGGTTTTTTAAAGATAGTTTGGTGAGCAGGAGGCTAGGAAATGAGAACTGCTGCTTGGTTGAGGATGCAATCATAGGGGTATGGAAAATGGTCCTTGTGTGCTGATTCAGCTTCTGGCTGGGGAACATGAGGCCAGTTAAATCACGAATCATGGGTCTGAGTGGAGTCAGCTGGTTGTCAGAAATGCAAAAGTCTGAAAAGACATCTCAAAAGGCTAATCTTATGTTCTACGTAGTGATGTTATTTACAGGAGTAATTGGGGAAGTTATAAACATTGTAACTTTCGGAACAATGGCTGGTAATTTTTTACTATGACTACATTTTAGTGGAATTCACACCCCTCTCATAATTCTAACCTTGTGGCTTTGTATTAGTTTTTATAAAGGCAGATTTGTTTGGGGAAAGACTATCATCATTTAAACTATAAAGTACATTTCTCCCAATGTTAGCTTGCTCCATGCCCAGGAACGATCAAGGGCAGTTTGAAGGTAAAAGGCAAGATGGAGTTTATTATATCAGATCTCTTTCACTGTCATAATTTTTTCCCTGTTACAATTTTTGTAAAGGACGTTTCACTCATAAGAATGTTGTTATTCTGTGCCTCAG
Seq C2 exon
GGAGAAGTTGGTCAAATTGGCCCAAGAGGGGAAGATGGCCCTGAAGGACCCAAAGGTCGAGCAGGCCCAACTGGAGACCCAGGTCCTTCAGGTCAAGCAGGAGAAAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000060718:ENST00000370096:29
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(21.8=100),PF0139113=Collagen=PU(22.4=94.4)
A:
NA
C2:
PF0139113=Collagen=PD(5.1=11.1),PF0139113=Collagen=FE(46.1=100),PF0139113=Collagen=PU(13.5=27.8)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
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