Special

HsaINT0039220 @ hg19

Intron Retention

Gene
ENSG00000197565 | COL4A6
Description
collagen, type IV, alpha 6 [Source:HGNC Symbol;Acc:2208]
Coordinates
chrX:107454902-107457458:-
Coord C1 exon
chrX:107457342-107457458
Coord A exon
chrX:107454971-107457341
Coord C2 exon
chrX:107454902-107454970
Length
2371 bp
Sequences
Splice sites
5' ss Seq
CCCGTATGC
5' ss Score
1.37
3' ss Seq
TTTTAAACTATTTTACTCAGGGG
3' ss Score
4.75
Exon sequences
Seq C1 exon
GGCCACCCTGGACAACCAGGCCCCAGAGGCCCACCTGGTCTGGATGGCTGTAATGGAACTCAAGGAGCTGTTGGATTTCCAGGCCCTGATGGCTATCCTGGGCTTCTCGGACCACCC
Seq A exon
GTATGCTGCCAGATATTTGCATTTTATTTCAAATGGCTTTGCTTGTCTCTACGTGTGCCCTTTTTCTGCCTCTCTGGAAACCTCAAGATTTTGTGGGGCAGCCACTACACACCCTTGTCCAATGTAGGAGTCAATACTGGCAGCACCACAACAGTAAAAGTCTAAAGAAGAATACCAGTTGCAGTGGGGTGTGCACATGCTACACTGCTTAGGGTTGCCTTTTTTTTAATGCAGCTTGTGAAATTGGCAAGATTGTTAAAAGGCTGTAGTAAATTTCATGGCAAAATACACACTTGGGCTATTTGACATGGTCCCACATCAGACAATATTGAGGAATGTTTGGAAGACTTATATGGGATCATGGAAGCACTAACCAAAACCCAAAGGGGCTTGCAAGCTTGGTCTATACCAGTGGTTTTTAACCAGAGGTGATTTTTGCCACTCAGGGGACATTTGGCAATTACTATTGATATTTTGAGGTCTCACAATTGGTGGTGTGCTACTGGCACAAGACAGCCCCCTCCCCAACATCTAGAAATCATTTGGCTCAAAGTGTCAATAATGCTGAGGTTGAGAAACCCTACTCTATAGTAACAGAGTTTGTGGCTACACTCCCACATCATAACCCTTGGTTATGGTATTGATAAGGTATTTATTGGATTCCAGTGTCACCACTTTTATTTAATTCTATTCATCCAGATAGGGCTCAGATATTTTGATCTAAGGGATCTCTAGTAAATACAATGCCCTTCCAGGCTGATTTTACAAGTGGCTGGAAAGAGTAAAATAACACATTTCAGACTCATTGTCAACCTCCCTTGAAATAATCTAAACTCATGAGGGCACTGATCTGAGATATTTAACTAGAAATCACTCCATTCATGAGACATGTTTTATAGCTACATGAATTAATTGACACTTCATTGGAAGAGCAGCACCACCACCTTCAGTGACCAGGTTGGGGTGTGGGTATATGTGTGAGAAAATGAGATAGATGGACAAAGCACAAGCCCCAGATTGGCATATAGGACTTTGACACCTAAGGACCAAATCAATATGCCGGGGGGTGGGGAGGTAAGGAAAGATGTATTGCTAACATAGGATGAGATAAGTGGGTTACAAAGTTCTCCAAAGATTGCCATGGCAACCAGGTATAGAACAAAACATTTCCATGAAAATCCAGCAAAGCAAGGACATGCTACCCCCTAAAAGGAGAAAATAAATGTTGAGGTAATAAATACCCATTGACAAAGGACAAAGGAAAAAACCTAGTTCTGTCTCTTAACTTAACCTCAAGCCTAAATAGGAACTTGGGCATGTATTTTACTAAGTGGAGATGTATCCTTTGCTGAATACCAAACAGATCATTCAGTTGGCTTTTTTGAAGCTTCTTTCAAGACAGTAGTGGCCACAAGAATAAAGTGAAACAGGCAGTGTTAGGAAAAAAAGTGAGAAAAAAAAAACGGTTTCTGCTCCTGGGATCACGTTGTTGTTTTATGATACCAATAATCCCTGTGCTGAAGGAATCAATCATTCAATAAATGCTTCAGTCCACAAAGCTTAGCCCTACCCCACATACTAATCCTGACTTCCCCTTAGGTGTAGGGACGTTGATTATCCCCAGGTGTACAAACTCTAACAGATATTAGCCAGCATCTGCCAGTAAGACAGCAAAAAATCTAGTTGAAAGATTGGAATTGTGTACTTTGAACCATTTTTCATGTTAGCAGTGAGATACACCAGCCTCTTAGACAGACTTTGAATCTGAAGTTGTGTGGTAGAAGTACAGGATGAAGGTAGTTTTGTAGATATCTTTTAGACCAGAGGTCTACAAACTGGACCACATGGCCTTTGGCTTGTGGCCTGTTTTTTTTTTTTTTAAATAATAAAATAAAAAGAAAGAAAGAAGAAGAGTATAAAACAGAGTTTAGATATGACCCAAAAGGCCTAAATTATTTACTATCTGGTTCTTTTCATAAAATTTTACTAACCTCTGTCCTAGACAAAGGTTCTGTCAGTGACCTATACCTGTGAGGGGTGAAGCAGCGAACTCTCCATTACATGAGTTATTTGTGGTTGTTCAGACCAGTACTCTGAATAGATGTAAAGTATCTGACTTTAACACATTTCAGACCCATTCAAACCCTTTCCCTTTACAGACTTCTGGCTTGGGGATTGGGAGGGCATATAGCTCTGAATCAGAGCACCCGGTCAAGGAATGTGTTTTGCCCCTTAGTACAGCCAATTTTGCCATAGAAAAAGCCACATGGTTTCAGGCTCTTGCTGTCCCATCCTCTATCTGATCAGATAATGCAATTAAAAAGACTGTAAGTGTGTGTATTTCTTCAATTTTTTAAACTATTTTACTCAG
Seq C2 exon
GGGCTTCCTGGTCAGAAAGGATCAAAAGGTGACCCTGTCCTTGCTCCAGGTAGTTTCAAAGGAATGAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000197565-COL4A6:NM_033641:6
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=0.899
Domain overlap (PFAM):

C1:
PF0139113=Collagen=FE(62.3=100)
A:
NA
C2:
PF0139113=Collagen=PD(19.7=52.2),PF0139113=Collagen=PU(11.9=30.4)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
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