Special

HsaINT0037883 @ hg19

Intron Retention

Gene
ENSG00000060718 | COL11A1
Description
collagen, type XI, alpha 1 [Source:HGNC Symbol;Acc:2186]
Coordinates
chr1:103477969-103480150:-
Coord C1 exon
chr1:103480067-103480150
Coord A exon
chr1:103478026-103480066
Coord C2 exon
chr1:103477969-103478025
Length
2041 bp
Sequences
Splice sites
5' ss Seq
CGGGTAAGA
5' ss Score
9.84
3' ss Seq
TGATATATTTTGTTTTCTAGATT
3' ss Score
9.68
Exon sequences
Seq C1 exon
TTCCGTTATGGTGGTGATGGTTCCAAAGGACCAACCATCTCTGCTCAGGAAGCTCAGGCTCAAGCTATTCTTCAGCAGGCTCGG
Seq A exon
GTAAGACAGGATAAACTTGCATTCCCACAAGATGACTGACTCTGTATCAAGTATATATGTGTGTACATACGGAAGATGCTACCATTATTAATAGAATATTTACTTCCGAATACTGTGTTAAACTTACTTGGAAAACTGCTAAAATTTTATTTGTTTTTCTAGTAGTAATGTTTATTAATTGAAAATTATAGTTAGGTAGTTGACCAATGCAATGTTGCCATTATATAATTCTAGCAGTTTCCCACCATAACACGCAAGATTTCTATTTTTTTTTCCCAAGAGTATTGATATATTTACACCTAGTGCACCTTATCTTTCACATCCAGTTTTACTCTGCTAACTTATAAGTCAATGATTGGTTATAATTAAGAGAATAAAATTTGAAATACATTTGTTCTTAATTTTCTGGATTATTTAACATATCATGGATAACACAGAAAATTAAATTTTTTGGGCATCATATATAAAAAAGAAACCTTCAAATTTCTTACCAACCCTAATCTTTATAATCTGTAGTATTTTTAAAATTTCAATTTATGTTTTTTAGTTTAAAGCTTCCACTACTTGTAGACTTATAAAATATAGAATTACATTTATGTTTTTTAATTAGTTTCATTGAAATTAGAATATACACAAGAAAATCAAAAGGATAGACCAGGAAGGAAATGGAATTCATATAACATTTTTATTCATAGTATTGGTTTTCTTTTTAAGGAAGAAGGAAATAAAGGATTTTTGTTTGGTATGGATATGGTTACCCACTTTCTAACCAATATAAATCACTTCTGTGATAAAATTTTTATGCATCATGATGAATTTATGCAGCATGTGTAAAAATATCTGAAAACATGAGTAAAAATTGTAATTCATCCTCAATATTTGTTTATGTCTTTCCTAAGTCTATTAATCTGAAAATATATCATTATTTGATTGTATCATGTTTAAAGATAATGAAAAATTAAAATATTTGTTTATTAGATTTTGGCATAATGCAAATCTAAAATTATTTAAAATAATTTACTAAAGATTTCTATAACTTATTTTATAAAATATATTCTTTTGAACGATTTTAAGGTAATTATTTGAACTTAAATATTTTATGAGGTCATTGAATTCCTCACTTTATTAGTCCTCTTAACCTACTTGAAAAATAGGTAGCAAGCATTATAATTCAATTTTTCAGATATTTAATCTCAAGGATTAAGAAGTATATTGTCAAAAATCTCATGGTGAGTCAGTAGTGATTTTGGAGATCCTACTGTTTTCATCTCGTGCACTTTTCTAATATGATTTTGCATTTATTTCTGTTGTATTATTTTTGATATCTTTGTGATAAATCTAAGTGTTCATCTGTTGAGCTCTCTAATATTCAAAAGTAGCACACAATACTAATTTAACATCTATCAAATTTTTATCTTTTGTACTGTATGTGTTTCAGCTTTTCAAGTATGCTAATTTCACATTTCTAATATTCAGTGTAACAATAGTGCATGTAATCAGTTTATTATGCGTATGATTATACAAAATAAAACATTCTTCTCTATAGCATTATATCTGAGATTTGTTAAAAGGCACATATTATCATAACACTTCCTGACCAGTTTTGTTTTATGGTGTCTGGCTTTGGTTATCATAATTTTTCCTAAAATATTGCTAAAAGAATTTTATTTAAAGCCTCTCAAATTGTGCCTACACATTTAAGAGAAAAAGGCTATGCATTATTCTTGAGTAAATTCAGAATAGTAAATTATCAGATATTAGTTGTTCTAAAATCTAGTTTAACTTTTATTTTTGATTAAGTCATAGCAATATATATTACAAGATTTTATATGTTAAAAAGTTTTTAAAATGTCTGATATTTACCTCTTTTGTCATTCTAGAAATTTGCAGTTCTTCAGTAACCTGACACTCTTTCTAGCATGTAGTTATTAAATCTGTGTTGATCATGTATTACTTAAGGGCAGCTTGTGCAGATTCATATTGTACTTTAATGTGCTCTTCCAGGAGAATATTACTGAATTTGATATATTTTGTTTTCTAG
Seq C2 exon
ATTGCTCTGAGAGGCCCACCTGGCCCAATGGGTCTAACTGGAAGACCAGGTCCTGTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000060718-COL11A1:NM_001190709:12
Average complexity
IR-S
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:
NO
A:
NA
C2:
PF0139113=Collagen=PU(25.8=84.2)


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

  • Genotype-Tissue Expression Project (GTEx)
  • Autistic and control brains
  • Pre-implantation embryo development