Special

HsaINT0037963 @ hg38

Intron Retention

Gene
ENSG00000111799 | COL12A1
Description
collagen type XII alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2188]
Coordinates
chr6:75148358-75151287:-
Coord C1 exon
chr6:75151141-75151287
Coord A exon
chr6:75148498-75151140
Coord C2 exon
chr6:75148358-75148497
Length
2643 bp
Sequences
Splice sites
5' ss Seq
CAGGTAAGT
5' ss Score
10.86
3' ss Seq
CCCTTTATTTCCATGTGTAGGTG
3' ss Score
10.51
Exon sequences
Seq C1 exon
GTATTAAAAATGCTGATGAAGTCGAATTAAAGATGATTGCAACTGATCCTGATGATACCCATGCATACAATGTGGCAGATTTTGAGTCACTCTCCAGGATAGTGGATGATCTCACCATTAATTTGTGTAACAGTGTCAAAGGTCCAG
Seq A exon
GTAAGTTTAACCCAGAGTTTCTCTCCCTCAGCACTGCTGGTATTTTGGGCCAAATAATTATTCTTTTGGGTGGGGGGGAGGGCACTATTTTGTGCACTATGAAATGTTTAGCAGTGTGAAAGGCCTCTGCCGGTTGGATGTCAGTAGCATCCCCTAAATTGTGGCAATTAAAAAGATCTTCGGTTGTTGCCAAATGTCTGCTGCAGAAAAAAACTGTCCCCAGTTGAGAATCACTGCATTAGTCACTGATTTTTTTTTCTGATTTGTTTCTCGTGATGGCACCTCAATGACTTCTAGCTTATTTGAGGATATATTTAGTTTATATCCTGCATACCTGCACCCTCCCCCACACAACATATATATAAATGGGAAGGGGTAGGAAGAGAGGGAAGGAGAGATGCTTTCTTTTCTGGTATATACCTATTGTCTTAAAGCATCTTCACTCCATTTAGTTACTACATTGCTATTGGATGGTTGTTCCCAGACTCTTGTTTTCCTCAGTTTTGGTACCTTTTTTAAATTTCCTAGTGTGAGCAGGAATGAAAGAGCAGTCTTTATATCTGATTTGCTTTGCCTCAACTGTAGATGATCAGATTTGAAACTTTACACTTATAATCCCTAAATATAAAGAGAAGCTACAATTTTACAGTTTAGACATTTAGAAATTATATAACCTCTTTTTACCAGTGAAGAAACTGAGATCTGGAGAAAAATTACTTGGTCTGGGTCAAATGTTTAAAGATGTTTTTAGGGGTATTAAAAAAGTAGATATAGCTAAGGAATTAGGATATTGAAATAAAATTATAGAACTGGATTTATACCAAAAAAGGATGGTGCATAATGATTACTCTCTGTGCAAATCATGGGACAAAACATGGTAATCACCAAATTTGAAGGTTTTTTGAAAATTAATGATAAAAATTATGGCTCTTATTATGTGAGAAAAATTTTATTTAAGTACATGTAGATTATGGTAAAATTGTCCTTCATTAATTTAATTTGGTTTTGGAAAAGTTGGAATAAGTTTAAGAAACAATGTGGTAGAAATGGTTCACTTGCTCTGGGTGCTAGGGGTATGTTTATTTGAATGTTCCCTCTTGGCTTTCTTTCTCCTAACTTTTGCAGATTTTCTTTTTTGAATTTTGAACAACAGATTGACCTTTTCCCTGGAGAAATAGACCAGCCTGGCAGCCAGAATTTGTAGGCTTCTGGCTCTTGATTAGCTGAGAGAGTTGTAGTTTTATTCCATTGGAGAGAACTTTGAGTGGGATGAAAACATCTTTTATCTGTTTTGCTTTTTTTAAAAAATGAACTATGTAATAGTTGCATTCATTCTAGTTTCCCAGACAGTAAAATTGCTTGATAATTTTGTAGGTTTGACTCTTACCCAAGTACAATAAAAGTTAAGATACTAAGAATGGAAAGGCTTTCCCCAGTTTTGGCTTGCACAAAAAGTAGAAAGAGTTTATACGAGAATGATTTGCCATGCTTATGGAGTTATTGGATTAATCCCTTTCTCTTTTAATTATTATTTGGGCCATTTTCCTGTTAGACATATTGAGCTTAATATTTCCATTTTCATCAGCATTTATTCCAGACACTGTTATGTATTAGTCATTTCACCTATATCCACCCACAGGGAGCACAATCACAGGCGGTAGGTTGTTCCCAGATTGAAAAACATGTGTTTCTTTGCACTCTCTCCAGTGATACATTGTCAGCTTCCTTTGTTATGCAACTAGATCCTGTTAGAGAATAGAATGAATGAAAAATCAATTCTGTCCTCACAGAGCATAACCTTTAGTTAAGGAGAGAAGACATGAGTATATAGAAACAAAATGATAATGAGGGCAGGGAAGTTGTGTGGTGCCAATAGTGATAGGGACAATGGAGAAGCTAAATTGTCAGGACCTAAATTCTTATTTACTGATTATATGTACAAGGGTAGAGAGAGGAGAAAGTATCAAAAGGTGATTCAGAGGTCTTAGTCTGTTCTCATGCTGCTAATAAAGACCTACCCAAGACTGGGTAATTTATAAAGGAAAGAGGTTTGATTGACTCACAGTTCCATGTGGCTGGGGAGGCCTCACAATCATGGAGGAAGAGCAAGGGAGGTCTTACATGGTGGCAGGCAAGAGAGAGAATGAGAGCCAAGTGAAAGAGTAAACCCTTATAAAAGCATTAGACCTCGTGAGACATTTACTACCACTAGAGTAGTATGGGGGAAACCACCCCCATGTTTCAATTATCTCCCTGTGGGTCCCTCCCACAACACTTGGGACTTATGGGAGCTACAATTCAAGATGAGATTCAGGTGGGGACACAGCAAAACCATATCGGGTCTTGAGTCTCAGTGACTTGTAAATTGGTAAAGTTTGTAAGGAAGAGGAGGATCAGGTTTTAAGGAAAGACAATGAGCTCATGTTTTAATCTTTTGAGGCTAGAAAACCTTTTAGTTACCTATTCATAACGGTCTTACAGGTGATGAGCCTCTAATACAGATTTATTGTAGCTACTTAGTATGTGAAAAGAAGTGTGTGAAAGCTTAGAATATGGAGCATAATATTGTTTCAATGTCATTTCAAATATTGTCACCTTTCTACAATAATGAGAAAAGTGTATACCCTTTATTTCCATGTGTAG
Seq C2 exon
GTGATTTGGAAGCACCTTCTAACTTAGTTATTTCTGAGCGAACCCATCGTTCTTTTAGAGTGAGCTGGACACCACCTTCTGACAGTGTGGATCGATATAAGGTGGAATACTATCCAGTTTCTGGAGGGAAACGTCAAGAA
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000111799:ENST00000322507:21
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.057 A=NA C2=0.106
Domain overlap (PFAM):

C1:
PF0009223=VWA=PD(21.4=74.0)
A:
NA
C2:
PF0004116=fn3=PU(53.8=91.5)


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