Special

HsaINT0038041 @ hg19

Intron Retention

Gene
ENSG00000197467 | COL13A1
Description
collagen, type XIII, alpha 1 [Source:HGNC Symbol;Acc:2190]
Coordinates
chr10:71690156-71692360:+
Coord C1 exon
chr10:71690156-71690308
Coord A exon
chr10:71690309-71692315
Coord C2 exon
chr10:71692316-71692360
Length
2007 bp
Sequences
Splice sites
5' ss Seq
CCGGTGAGT
5' ss Score
10.9
3' ss Seq
GTGGTGTTTTGTGCCCACAGGGA
3' ss Score
10.39
Exon sequences
Seq C1 exon
GGACCTCGCGGTAAACCAGGAGACATGGGCCCTCCTGGTCCCCAAGGCCCCCCAGGAAAGGATGGACCTCCAGGAGTGAAGGGAGAAAACGGGCACCCAGGGAGCCCAGGAGAGAAGGGGGAAAAAGGGGAGACAGGACAAGCAGGCTCACCG
Seq A exon
GTGAGTGGCAGGGCTGGCTGCCCTTCCGTGCATACACCACTCCCAAGCATGACGCCAGCTTTGCAGGGCTTTGCACTTTGCATGATGTGAGCTGCTGCCTGGGCTAGAAACCTGGGGCCAGGGCTTAGGGGTGGAGGATTCACTCAGCTTCCCCTCAAGTCACTCACTTTATGAAGGCCAGTTTCCCGACTCAGGAGACCTGAGTTGTGCTCTGTCATCTGTATCCTTGGGAAAGCCACTCACTGTTGCAGAGTCTCCGTCTCCTCATCTCTAAACTGGCGATAATAATGTTTTCCCTGGATACCTCACTGGATTGTTGGGAAAGAGATGAAGACATGGTTTAGAGCTGCCTCTTTGGAAAGTGTACAGAAGCCCTATACCCGGGAGAGGCTGCATGTACAGAAACGGGGCCTTCGCCCAGTCCACTAGGCTGCTAACTTGACTTAGGGGCCTTCTCTGGGTCTCAGGGGTTTCCATCTGTGAAATGGGTGCCATCCTAGACACCTACCCTTGGAGCAAGGGAGCCACATCCTGTGCAGGCCACAGTTGGTCACACTCAGCAAGACCACCTTGAGCTCCACTAACAGAAATCATTGTCAGTCTGTAGGGTCTAGATGGCCCAACTGGGGAGAGGAGAACATGGTGGCCAGAGCAGACCCAGAGTGGCAGGATTGCCTAATCCAGCTGGGCTCCTGAGGTTTACAGTGAAGCCAGAGGGCTGGGTGTCAAGGTTGCCTGCAGGCAGCCACAGATGAGGGTCCTCCTGGGGGCCACCAGCCTAGTGGGTGCCTGACACTGTGACGAGGCTGCCCTAATCCCAAGCCTGCCGACCCAGCCTGGGAGCAGGCAGGGAGGGTCCTCTTAACAAGCAGCTACTTCATTTGAGTGTAAACAGGAGTTGCATCTTCCTTGGCTCACGGTATGATGGCCTCTAGGAGCACCAACCTAGTTCGACGGTGCTAGAATCTTGGTCTCAGAATTCTCCTCTAGGAAGTGGAAAGAGCCTCAGAGGTCAACCAGTCCCAAGTCTGACCCAGTGCAGGACTCCTCACTCAACCGGCACAGGCAGGCAGCTCACTGCCTCCAGACCTGTCCACTGCACCATGGGGCAGCCCCAGGATGGAGGGAGCATTCCTGGATATGGTGTGGAAGCTCCCTTGTCAGCCTCCCCGAGTTGACCCCTCAGAGCCTCTGGCCTCTGGAGCCATATTTATTATCTATTGCTGCATAACTAATCACTGCAAACGTAGCGGCCTAAGAAAATACACACTTATTGGCACATAGTTTCTGTGGGTCAGGAATTCAGGCACATCCTAGTTGGGTCCTCTGCCCATGGTCTCATGAGGCTGCAATTAATGTCTCAGCCAACTGTATTCTCATCTGGAGCTAGGGATCCCCTTCCAAGCTACTGGTATTGGCAGAATCCAGTTCCTTGCTGGAACAGAACTCAGCTCCTAGAGGCCACCTACAGTTCCTGCCACCTGCGCCCCTGCCCTCCCCACCTCCCGCAGAGTAGACAGTTCACATTATAGCAACTGGCATCTTCAAGGACAAGGCCAGCAGTAGGGTCTCTCTAGTGTCTAGTGCTAGCAAGACAGAGCTGTGTGCACGTGTGTTTGTGTGTTCATGTAACATATTTGTAACATAATCTTAATATATGTTATATGTCACCATCTGTATGACATGTATGTTATAATCTGCAACATAATCATAGAAGTGAGGTCCCACCACCTTTGCCATGTGCCTTACTCCACGGCTAAGAAACAAGTCACAGGTCACCCTAAGGCCTGTACGCTGCAGAGTCCACAGAGAGTATCAGCCTCTCCTCCCCTGTACTAGAGCCTCAGATTCTGTCCTGCAGGCTGACACCTCCACATCCTCCATGGTGTTCCTTGTTGACCCCTAGACCAGTCACGTCCCAGTCTAGTTTGTCACAGATGTGAGGGTGCGTCTGTCCCAGGCTTTCACAAGGGCTGGCATTCATGCAGTGGTGTTTTGTGCCCACAG
Seq C2 exon
GGAGAGAAAGGAGAAGCCGGGGAGAAGGGCAATCCAGGAGCAGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000197467-COL13A1:NM_080800:28
Average complexity
IR-C
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(37.7=45.1),PF0139113=Collagen=PU(71.0=86.3)
A:
NA
C2:
PF0139113=Collagen=FE(18.4=100),PF0139113=Collagen=PU(2.8=13.3)


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