Special

HsaINT0039280 @ hg19

Intron Retention

Gene
ENSG00000130635 | COL5A1
Description
collagen, type V, alpha 1 [Source:HGNC Symbol;Acc:2209]
Coordinates
chr9:137714844-137715315:+
Coord C1 exon
chr9:137714844-137714879
Coord A exon
chr9:137714880-137715261
Coord C2 exon
chr9:137715262-137715315
Length
382 bp
Sequences
Splice sites
5' ss Seq
TCGGTAAGT
5' ss Score
11.78
3' ss Seq
ATTCTTTTCTTTCTCCCCAGGGT
3' ss Score
11.84
Exon sequences
Seq C1 exon
GGTCCGCCTGGTCCAAAAGGTGCTAAGGGCTCCTCG
Seq A exon
GTAAGTAACATGCTGCCCAGCCAGGCCAATGCCTGGAAGGTAGGGGAGGGCGACGGGTCCCCTGGCACGGGAACAAACTACCCAGACAACCGTCCTAGCTCAGGCCCTGCTGCTCACGATCCTCCCATCTTTCTACACTGACCCATGGCGGACTGAGGCAGGTGGGCTGCTCGCCGCCTGCCCTAGGAAGGGCTCCATCCCTCTCTGTTCTCATCTCAAGGATCCAGGAGGGTACAGGGGTCTCTGCCATTCTCTTCTCTGCTGTGGCTGATAGGGCCACCTCCCCCACATAGGTCTCCAGGGACCATTCTAGAGCTGAAGGTGGATTCAAAGTCCCCTCATACCTCTGTGACCAAGGGTTGATTCTTTTCTTTCTCCCCAG
Seq C2 exon
GGTCCAACTGGCCCGAAGGGTGAGGCAGGCCACCCAGGACCCCCAGGCCCCCCG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000130635-COL5A1:NM_000093:60
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:
PF0139113=Collagen=FE(17.5=100)
A:
NA
C2:
PF0139113=Collagen=FE(27.0=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping 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