Special

HsaINT0039569 @ hg38

Intron Retention

Gene
ENSG00000172752 | COL6A5
Description
collagen type VI alpha 5 chain [Source:HGNC Symbol;Acc:HGNC:26674]
Coordinates
chr3:130440166-130443566:+
Coord C1 exon
chr3:130440166-130440825
Coord A exon
chr3:130440826-130443475
Coord C2 exon
chr3:130443476-130443566
Length
2650 bp
Sequences
Splice sites
5' ss Seq
GGCGTAAGT
5' ss Score
9.39
3' ss Seq
TAACTTTGTTCTCTCAATAGGGG
3' ss Score
9.67
Exon sequences
Seq C1 exon
ATAAATGTTTTCCAAATGCTTGCATTCGAGAGGCTTTCTTACCTGAAGATTCATACATGGATGTAGTCTTCCTCATAGACAATTCTCGGAATATAGCAAAGGATGAGTTTAAGGCTGTGAAAGCCTTGGTGAGCTCAGTGATTGACAACTTCAACATTGCTTCAGACCCTTTAATCTCAGACTCTGGTGATAGGATTGCTTTGTTGAGCTATTCTCCTTGGGAAAGTTCCAGGAGAAAGATGGGTACAGTAAAAACAGAGTTTGATTTCATCACTTATGACAACCAACTCCTAATGAAGAATCACATCCAGACTTCCTTCCAACAGCTAAATGGAGAAGCAACAATTGGTCGTGCCCTACTGTGGACCACTGAAAATCTTTTTCCAGAAACACCCTATCTAAGAAAACACAAGGTCATCTTTGTGGTCTCAGCTGGAGAAAATTATGAGAGAAAAGAATTTGTAAAAATGATGGCTTTGAGGGCTAAGTGTCAAGGCTACGTCATATTTGTGATTTCTCTGGGCTCTACACGTAAGGATGACATGGAGGAGTTAGCCAGCTACCCACTTGATCAACACCTGATACAGCTTGGGAGAATACATAAACCAGATCTGAATTATATTGCGAAGTTCTTAAAGCCATTTTTATACTCGGTCAGGC
Seq A exon
GTAAGTTATTATTTCATTGTTTGTCTTTTTTTTAATAAGCTAGTGTTTGTTAATACAGTATTGATAACCTATTTTTGTATCTATAGCTAATCTAAACATAATTTATGAATTAGATGGTGAGATAGGGGCAGGAATGGATCATTTGCTGGTTATACCCTGTTTATATCCTGGTCACAAAATGGTGAGGCCTGAGGCCTTTTTTTATGATAGTGTGTCTTTTAGCCAAACTCTCAGCACTAGAAAGCCACAGAGTGACTAGAGGTCGTATGAATCACATTTGCTCAAGAAGTTCTAGCAGCAGTTAGGTGATTTCAGAAGAACATTCACGTAAAAGTTTTACTTGCTATACCTGTTTTATTTCCAACTTTGGCACACCCTGGAGACCTGTGTGAGGATGTGAAGATAGCAAAGTCCTGGGCATGCACATCACCCAGGAATCTTGTTAAAATGCAGGATATTCTTACTGAGGATATCTAGGGTGAAGCCTGAGATTCTACATTTCTAACAGATACTGCAGTAATGTCAATGCTGCTGGTTCATGGATCACATGGCTCTAGGCCAGTGCACTACAAAGGGTTGCTCATTGCATGAGTGCCAGGCTACAAATTGATGTATAAAGAAATAAACACACAAATTGAGAGTAAACATCTAGAAACTTTTAAGGCAATTTGACATTGATTGCTGCAGCGTACAGTTGCATGACCAGTGGACTCTGTCTCATTGAACAGGATGTATCAGTCTGCAAAGAACTAGAAATAAGAATACCTCGTCCTCTATCACAGATGGTTTGGAAAAATGCTCTTCTAGAGCAATTGTTCTCAATATGGCACAATTTGCCCCAGGGGACATTTGGAAATGCCTGGAGGCATTATTTGACAGTCACAACTTGGGGATGCTACTAGTATCAAGTAAATAGAGGTCAGGGATATTGCTAAACATCCTACAATTCACAGGACAGACCCCCCACCACAACAAAGAATAATACATCCCCAAAAGTCAATAACACTGATGTTGAGAAACACTTCTCCATAATATCCCACAGAATCAGAGCTGAACCTTTTCTTTCTGGAAATCTGACAGGTTTAGAAGTAAACTTGGCTGGAATTAATTCCACCACTCTACAATCCCAGTTTCCTTGCTATTCAAAGGATCACCCCACAACACCACAGTGATAATGTCTTGAGCCTTCACTCTTCATTGCAAGGAGAGCTCCACCTTTCTCCTGTGATTCATATTCAATTAAAGAATCCAATAATTGCCCTCTTGGGAACACTGTTATTTCTTTACATCTAAGATGCCCTCAATTGTATAATGTAAAGGAAAAAAATGTTTCCAATTAAATTTTGATACCAACTTTCCTATTAGAGCATTTTGTTTTATAGCAATTGAAAGAGTTCTTTTGGATGTATAGTAAATATATCACTCCTGTGCATGCATAAAAAGAAAATCTATGTGAAATAGGCAGGTTAAGGCACTCCTAAAACAACTTCTGATTCAGAATTTGACTCTTGTGAGCTACTTCTTGGCTCAGAGTCATTGGTATCCATTTTTTTCTATGCAATTTTGTTCTTTGTGCCATTAAGATTGATGATTATGCAATATTTGTAAAAGACTATAAAACAACTCAAAGATGGTCATGCTGGGCTGTTAAGTGGCTTTGCAATCATGTAGAAGTAGCCTACTGTTGACTTCCAGCTGGGAAGTGTTAAACACACCCAATTCGCTGCCTTCCCACAACCACTTGGTTTGTAGGAGTGAAAAGGCTCCTCTGCTGGTATTTATGGGAATGTTTTCAAACTGCTCTCCCCAATTCTACAAGTTTTGGTGCTGGCATGTTTGCTGTTCCCACATGCACAGGCAATGACCACTGCATCACAATTCTTGCCCACCCAACAGTAAGTGTCAGATGCAATTAATCAGAAGATATATTTTCATTTTAAAGAAATAGAAAAAAGGAAAGAAATGCTTATCTTAGTATTTGAAAATGTGATTATTATAAAACTACAGATGTTATTTGAGATATTTTCATAGATCCTTGGATCAGTCAATGGCTGAAGGCCTTCTTTAACTAAAATCTTTTATTTTCCAGAATGGGACAGGGTAACATACTTCTCCATATTCCAAAATTTATAGAACAACATCAGGAAGGGGATAAATAGGCATATTATTTAGACCAGTAAGGTAAAATCTTGTCTATGATTCTTTTCCTCATAGGAATCAGTATTAGTGGGTGCAGAAGCACAGAAATGATATCAGTATCAAGTAATGAAACATTACCTTGTCTCTGTTTGATCCGTTAGCGTAAGTCTGGGTGAAAAACCTTTGATGAATCAGAATAGAGTATCTCTTAGATTATGTTAGCCTGAGCATGTGAAAATCATGTTTCCCTGCATCACAACTAGCTCTTAGATGAACAATTTGAGGAGGTCTGTTTCCATGACTCTGGTAATCCTTTGGCTGCTAAAACACTCTGAAATCAAATTTTGAGTGCTATTTCTAACTGCTGTTTTCTGTTTTCACCCCAGCCAAATTTTGCTGAAATATGTTAGTGACATTAGTTGCTTCAAGAGGATTCCTGTTGGGATTCTCTTTACCTAGGAAACATCATTTCCAGTTTTAAAATCTAACTATAACTTTGTTCTCTCAATAG
Seq C2 exon
GGGGATTCAATCAGTACCCACCACCGATGCTTGAGGATGCCTGTAGACTCATCAATTTAGGAGGAGAGAATATTCAAAATGATGGTTTCCA
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000172752:ENST00000312481:35
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.000 A=NA C2=0.018
Domain overlap (PFAM):

C1:
PF0009223=VWA=WD(100=81.0)
A:
NA
C2:
NO


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