Special

HsaINT0039277 @ hg38

Intron Retention

Gene
ENSG00000130635 | COL5A1
Description
collagen type V alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2209]
Coordinates
chr9:134820116-134822150:+
Coord C1 exon
chr9:134820116-134820223
Coord A exon
chr9:134820224-134822096
Coord C2 exon
chr9:134822097-134822150
Length
1873 bp
Sequences
Splice sites
5' ss Seq
CAGGTGCGT
5' ss Score
9.73
3' ss Seq
CATTTTCTGGTCCTTTTCAGGGT
3' ss Score
11.17
Exon sequences
Seq C1 exon
GGTCATCCAGGCCTGATCGGGCTCATCGGTCCTCCGGGTGAACAGGGTGAGAAGGGCGACCGTGGTCTCCCTGGCCCCCAGGGCTCCTCCGGTCCTAAGGGAGAACAG
Seq A exon
GTGCGTGAGATGGCACTTCTTGCATGTGGGCTGTCGAGAGGCATTTTAGATCCCTGGGGCAGGCACCCAGGGGACAGGAGGCCCATCAGAGCCCGGAAGGACGTCCACACGTCGGTTGAGTCCGGTCATCCTGCTTGGCAGATGGGAACACTGACGGGCTGGGCTTGCCCAGGTGCACAGTGAGCTGGGCAGAGCCGTCTCCCAGCTCCATGCCCTGACTGGCAGGCGGGGCTTCCTCCTCATGACCGTGGTGTCCCCCAGAGCTGGAGGGACTCGGAAGTCAGGTCATTCTGCCTGGTTCCCAGCCCTGTGGGAGAGCCTGTCACCCACCGCTTGCCCAGGAGGTCACTGGTGACAACCAGCCGTGTTTGCCAGAGCTGCGGGCAGAGTGGCTGTTCTGGCTCCTGCTTCCACCTTGTCCCCAGCTGCCCCCAAACTGTAGCTCATTGGAGTTTGCAGCCTCTGCAAACCATAGCCAAGGAAACGCCATGCAGAGAGCTTCACTCTGTCCCACAACTCTGAGTGACTTGGAAGTGGCCTGGGGAGGGTGACGTGTGCCATGGAGGCAGGAGAGGGGATGAGGTGACCTGTAGTGCCTCTGTCCTTCCCCCATGAGGGCCACGGGTCCTTATTCCTGTGTGGGAATCTTTCCGTCCCGAGCAAGGTGTGACGGACACACACACGCACAGTATGCTGTGCCCACCCACGCCCATGCCTCATAGGATGCGGGGGACAGGGCAGGAGCAGGCAGAGCCCCTGGAGGCTGGGAGTAAGGTGGCACCCTCACTATGGGCCCGGGGAAGGTTGCAGGACATGGCTGAAGGGTGGAGCTCATTGCAAACCCTACCTCACTGGCCAGTGTCCTCCATGCCATTGACTGTTTTCCTCTGCCGGTATCCCCAGGCCACAGCAGGGTCGTCGGAGGAGTGCCGCCCAGGGTGTGGTGGCCCGGCAACCACGAGAATTAGAGAGGCATCCAGGGTCCCCACGGCCAGCGGGGAAAGCACCCCTGTGTCCACCCTGTTTGCTCACCTGCCCTCACCCCAAACCATGGTCTTGGCGGCATTGCTGATGAAGGTGTCGGGTTGGTGTGCAGGCTTGGGTAGTTGTGGGGTCCTTACAATGAGCCACAGCCCAAGTTCCTGCAGGGACAAGGTGAAGGGAGGGAAGCGCTCCCTCCCCAGTGAAATACGGCCATCAGCCCTCCGCTACCCTCGCCCCCAGCTTCTGCCCGGAGAGAGCTCTGAGTGGAATCCAGGGCTGTAGGGAGAGAGGCTGCAGGTGGCTCCAGCTGCCCGTGGCAAAGCTGGTCAAAGCTGTTCTGTGCCAGCAGCTCAGTCTGGGAGGGAGTCAGTGGGGAGAAGGGGTCTGAGCGGAGGTTCCACGCTCCAAGGATGCAGAAAGCACATTTACAGGCAGGACAGGACAGTCAGCATGGATGGGACTCCCTGCCCAACCCCTCCGGGCTTAGTTCTAGAGGGGAGACTAACACCATGAGCAGGAAACAGCAAGAGGGGCCCAAGCCAGGGCCACAATGTCAGGGCAGTGGTTTCTGTATTTCCAAATGAACGTGAAAAGAGGTGCTCAGCCTGAAGTCCTCGGTGGCCTGGGGGATGAGAGTGAGTTCCTGGCAGCCCAGCCGGGGGAGCAGTGCCGAGGGCTGGCAGCCTTGGGGTGGATGCTCAGGTCGATGGCTCCCCTGACATGCACAGCCCAGGATCAGAAAGCAGCCACAGGAGGCTGCTGAGGGGCCAAAGGGCATACCGTGGGGAAGGGACAGGGGAGCCGAGGGGTGTGGCTGGGTAGCAGGGTTGCAGCCCCGCAGCTCCTCCTCGTCTGAAGGTGATAACCTGCATTTTCTGGTCCTTTTCAG
Seq C2 exon
GGTATCACTGGTCCTTCTGGCCCGATTGGGCCTCCTGGGCCCCCTGGCCTGCCG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000130635:ENST00000371817:58
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(9.0=16.7),PF0139113=Collagen=FE(38.9=100),PF0139113=Collagen=PU(3.3=5.6)
A:
NA
C2:
PF0139113=Collagen=PD(17.9=66.7),PF0139113=Collagen=FE(27.0=100)


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

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