Special

HsaINT0007985 @ hg19

Intron Retention

Gene
ENSG00000101280 | ANGPT4
Description
angiopoietin 4 [Source:HGNC Symbol;Acc:487]
Coordinates
chr20:865721-869082:-
Coord C1 exon
chr20:868961-869082
Coord A exon
chr20:865969-868960
Coord C2 exon
chr20:865721-865968
Length
2992 bp
Sequences
Splice sites
5' ss Seq
CAGGTGGGT
5' ss Score
8.56
3' ss Seq
GTGCGCCCCCTACCCCGCAGCGC
3' ss Score
9.04
Exon sequences
Seq C1 exon
CTCCTGAACCAGACATCAAGAATGGATGCCCAGATGCCAGAGACCTTTCTGTCCACCAACAAGCTGGAGAACCAGCTGCTGCTACAGAGGCAGAAGCTCCAGCAGCTTCAGGGCCAAAACAG
Seq A exon
GTGGGTGTGGCACCTGGCACCAGACTAGGACAGGGGCTGGGGCTGGAGTCAAGTTTAGGACCTAGGGCAGGCACCAGAGCCAGGGCTAGGACTGGGGCTGGAGCCAGGACCGGAAGCTGGACGTGGGCTGGTGTCTGGGATAGGGCCTGCAGCCAGACCTAGGAGCTTGGATTAGGATTGGGGCAAGGAGGTATCCTGGGAGTTAGGGCTGAAACTAGAGCTGGGAATAGCCCCTGCTGGGGAAGGACTGAAACCAGGGTTGGAGTCTAGACTGAGGCTGGAAATGAGAGTGGATACGGGGCTGGGCTAGGAGCCAGGCAAACACATTGCCTGGCCCCTGCACTGGGTGGGACAGGGGATAGGCATCTTCCTGGGGCCCAGGACACCCTGATTCTTTCTTTCCCTTTCCTTCCTTCCTTCCTTCCTTCCTCCTTCTTTTATTTATCTCGTAAATTTTAACAGCTTTATTGAGATCTAATTCACCCACCATACTATTCATCCGGTAAACTTTATTGGCTTTACTTCTTTGCAAATAAATAAATCTGGTGCTATCTACGATTCCTTTCCCAGAAACAACCACAGTTACCAGGTTCTTGTCCACACTATCAGAGAGTCTTTGCATTTATAAGCAAATGGGCATCAGGGGAACACCCTTTAAATTACAAAAAAAAAAAAAAAAAAGCGGTCATGAGGTTTAGATAAAGCAGAAAAATCTGGCAGCTAAGGCTGATTTCACCTCAGTTTCAAGCTGAGTGAAGAAAAAAAGCTGCCAAAGTCAGGGTTCTGGAGAAGGCAAAATCTACCCACTGAACAAGCCACAGGCCTGTGAATCAGGCAAGATGTTGTTGTTCACATGCCGGTTCAGGATAAGGCCATAAGATCCCCCAGCTCTCTCTAATCTGGGTGCAATTAATGACAATCTGCCCATCTTCTTATTCTCCCAACCCAAGGTCTCAGTGGCAAGGACTGGGACACTTTCAATGACTCTAAATTAACACTAGGTGTCTAGAAATCAGTGAGGATGGAGGATGTCATCGGTAAACTCTTGGCCCATGAAGACAGGGCAGGAATTCTAGAATTTCAGTGTGCCCCAATTCTCTCTTTTCCTGCAGCATAATTGGGAGTCCAGAGGAAATTTCTTCTGCCCTAGCTGGACTCAATTTCTTAGTCTGCAGAATGAGTTGGCACAAGTGGATATACAGTAAAATGTCTCCCTCCCAGCCCTGTCTCTCAGCCACCCACCCAAGCCAGAGGTAGCCACTGTTCCTAGTTTCTTGTGTATCCTTCCATTCATTCAACCAACAATTATTTTTCAAACTCTTTTCATGTGTCAGGCACTATTGTAGACACTGTGGATACAGAAGTGAACAAAGAGACAAAAGCCCCTGTCCTCGTGAAGCTGACATCCTATAAGCTGACATTCCAGGGTTTCTTATGAATATGCAAACACATACATACAGAAGATTGCTAACTTACAATGGTTGGGCTTACAATTTTGTGACTTAACAGTGGTATGAAAGTGATACACATGCAGTAGAAACCGTACTTTGAGTACCCATACAACCATTCGGTTTTTCTCTTTCAGTACAATATCAATACCTTACATAAGCTACTCAACATTTTGTTATAAAATAGGTTTTGTGCTAGATGATCGTGCCCAATCACAGGCTAATGTAAGTGTTCTAAGCATGTTTAAGATGGTCTAGGCTAAGCTAGGATGTTCAGCAGGTTAGGTGTATTAAATGAGTTTTTGACTTAGGACATTTTCAACTTACGATGGCTTTATTAGGACATAGCCCCATCATACATTTTGGAGCATCTGTACATTCCCATTTTTATCCTTTTTAAGCCCAAATGTAGCCTACTACTTGTTTATACCTTGTTTCTACAAATTATTATTCAGTTACCTTGGAAAGATTCTATAACTGCATGACATGCTTGCTCATTTTTTTCTCCACCTTTATAATGCTCCACCATATGTGGTCCCTGCTTTTATTCCTCCAGTCCCCAGTTAATGGATATTGAGGTTGCTTCCAGCCTTTTACTAATCCAACCAGTGATACGATGAGTAACATTTCCATATCTCATTTCACACACATGTGAGTAAATCTGGAGGATAAAATGTCCAAAAAGAAAGAGCTGAGTCTAAGGCTTTCTTTTGAAAAACTCCTCTTTGCTTCTAAATCCATTACAAAAAATGTCTCTTGATTATTATAATATCATCGGACAACAGGAACCTGTACAAAATAAAAGTGAAAGTTGGGCCCTCCATCCTGCCCCCATCTTCCTCCTCTCCATCTTCATCCACTCAAACCTGCTCTGCAGAAGTCACAGCACTTGAGGGAATTTCTTTCATATTCTTCCCAAACACAGGCACCACTGCGGTCTTTCCAGCCTTCTCCTATATGTTCACCCCATTTCTCTTTATTTACATTAATACTTTCTTTCTTCTCTTGCCACACATGGGGTTAGGCTTGATGTGCCCCAAGTCCTGGGCATCTTTCCAATTCTGTGCAAATGCCTCCTCCTTCATGACTGCGGAACATTTCCAGGGACGCCAAAACGCAACGGATTCAGCCAGTCCTGGCTTTTGGGCATCTAGGCTATATCTTTTTTGGTTGGTTGGTTAGTTTGTTTTTCTATTACAAGCAAGTCCCCAGGGCCATTCTTGACCATGCTCCCTAGAGGATAACTCCTGAGAGTAGACTGCTGGGTCAAAAAGCAAGCACAGTTGGGATTTGATAATAGCTACCCAGTTGCTGGTGTCCCTCCCACACCACCTCTTTCTTCCACTAAACCTCAATCTATATTACTCCAGGGCCGGGTATCTCTTTTCTCCCCTCCTCAATCTGTGCCTACAGTGGGCACAGGACGTTCCACCACACTTGAGTCTCATCGTCGGGCTGCAGGGACTCCAGGGCCGGGGAGGCGCGCGGGGGTGCGTGCTTCGCGAGGATGCCAGGCTCACCTCTGTGCGCCCCCTACCCCGCAG
Seq C2 exon
CGCGCTCGAGAAGCGGTTGCAGGCCCTGGAGACCAAGCAGCAGGAGGAGCTGGCCAGCATCCTCAGCAAGAAGGCGAAGCTGCTGAACACGCTGAGCCGCCAGAGCGCCGCCCTCACCAACATCGAGCGCGGCCTGCGCGGTGTCAGGCACAACTCCAGCCTCCTGCAGGACCAGCAGCACAGCCTGCGCCAGCTGCTGGTGTTGTTGCGGCACCTGGTGCAAGAAAGGGCTAACGCCTCGGCCCCGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000101280-ANGPT4:NM_015985:3
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.390 A=NA C2=0.024
Domain overlap (PFAM):

C1:
NO
A:
NA
C2:
NO


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

  • Autistic and control brains
  • Pre-implantation embryo development