Special

HsaINT0070799 @ hg38

Intron Retention

Gene
ENSG00000115806 | GORASP2
Description
golgi reassembly stacking protein 2 [Source:HGNC Symbol;Acc:HGNC:17500]
Coordinates
chr2:170951328-170954782:+
Coord C1 exon
chr2:170951328-170951458
Coord A exon
chr2:170951459-170954649
Coord C2 exon
chr2:170954650-170954782
Length
3191 bp
Sequences
Splice sites
5' ss Seq
CAGGTAAGG
5' ss Score
11.08
3' ss Seq
AGAAAAAAATGTTTTTATAGCCT
3' ss Score
2.56
Exon sequences
Seq C1 exon
TCTGAAGATCTATTCAGCCTTATCGAAACACATGAAGCAAAACCATTGAAACTGTATGTGTACAACACAGACACTGATAACTGTCGAGAAGTGATTATTACACCAAATTCTGCATGGGGTGGAGAAGGCAG
Seq A exon
GTAAGGTCATTTTTTAGACTAAGTTATGACTGCTTAAACATACCAGTCAGATATGTTGCAGACATTGATTGTTTTTATTTTGAAAGAAATTACTGGTTTATTTTAAGACTCCTCTTAAAAAAAAGGGAAGAGCTAGTCTAGAATATTGAAACCAATTTTTTTAAAGTACATATCTAGGGAACATAGTATATATACTATAGTCCTTTTCTTTACTAACCTAAGAGCTAACAGCATTTCTTTTTAATTGAGAAATTATTGCGCATAAGCCATAATTATAGAAAAGCCTAGAATTTGGAAACATTCCACATGTTTTCAAAAGTTCTAATCCCATGCTGGGAAAAGGATAACTTAGTTGCTGCAGGCAGGAAAAGCTTCCGTTTGCTCACAGTATCTTTACCCACACTACCTGAGATTCTCCAGCTGAATGTTTCGCCACAAGTATTCTAACTTGTTGCAGTTTGAGAAAAGTAAGATAGATGTGTCATCCAAGAGTCTGGCCTATATGGGGCAATACTTGATCAAATTATCATTGTCCATTGCCCAGGTTTGTAAATGCCCAGAAATAGGATCTATTCGAGGCATTCAAAATTTATTCATTACAAGAGGCACTTCCTCATATAAACTACATTTGCAGAGAAGCTGCTATATTTGAATGACAAATTTTCAGTTTGCAATAGAAAAATACCCCCTCTCTAGTTAGAAGAATACTCAGGTCAGATTAGTACCACAAGAGTGCCTGCTGAGCATGGAATCAAACTGGAGGAAGAGATTCTGTGGACAGTGAAGACCAACAGCAAAGAACATCACATATTCTTTCATTTTTAATTATGTTAACTAAATTTGGCTACATTCTTTGGAAGACATTTTTTCTTTTGATGTGTTTAATACTGTCAGTTGGCCATTGCATTAGCTAGGCCCATACAGAACATTTTCGTCAGTCTGCCTCTGACCATGCATTTGGTCTTTTTGTGCTTCTGTTTTTATTCCTTCCTCAGAGGCTGACCACATTTCATTTATTAAATCTTATTTCTCTTAATTTCATTCTTAGGCTGTCTTTAAGTTTGCCCAGGGTCTTGCTGTTGCCTCAAGTGCATTGTCTATTACCACTTAATTACTTTGACCAATAAGCACCTTGTTTTCAAATGTAGCTACCTCTGAAAGGCCATAATTGATCACTATAAATTATTTAATCTTTATTTCTCTAAATCCCAGTCCAGTGAGAATTGCAGGGTTTTGTTTGTTTGTTTGGAGACAGCGTCTTGCTCTCTGGGCTGGAGCACAATCATAGTTCACTGCAGCCTTTAACTCCTGGGCTCAAGCTGTCCTCCCGCCTCAGCTTCCTGAGTACCTGGGACTACAGGTGTACACACTGTACTTGGCTAATTTAGAAACTCTTTTTTAGAGATGGGGCCTTGCTTTGTTTCCCAGGCTAGTCTTGAACTCTTCGCTTCAAGCAATCTTCCCACCTTGGCCTCCCAAAGTCCTGAGATTATAGGTGTGATCTTCCATGCCTGGCCGAATTGCAGTTTTGATTGTGAGGGAAGAAGGGAAGAAGGAACAAATAATTGTGAGATGAAGCATCATTGTGCATATCAGACTGGTAAAGGAGGAGCTAGGCCTGGCATGGTGGCTCACGCCTGTAGTACTACCGCTTTGGGAGGCTGAGGCGGGTGGATCACTTGAACTCAGGAGTTCAGTACCAGCCTGGGCAACCTGAAGAACCGTTGTCTCTACAAAAAATACAAAAATTAGCCAGATGTGGTGGCATGCACCTATAGTCCCAGCTACTCAGGAGGCTCAGGCGGGAGGATTGCTTGAGCCCAGGAGGCAGAGGTCGCAGTGAGCCAAGATCATGCCACTGTGCTACAGCCTGGGCAACAGAATAATAAATTGTCTTAATAAATAAATAAATAAATAAATAAATAAAATTAAAAAGGCTGAAGTTGGCTACTGCCTGCTCACCCAGCTTTTGGTGGCAGTGGAGATAATAGATGATGTGGCAGGAGAAGGGCACAGAGGTATTCATGCATGGCCTACTCTGAAATTGTCAAGTTGTTTGGGAAATAAAAGACATCATGATGGAAACATAAGTTGGAACCTGATTATGGAGAGCCTTAAATACCACGGTCAGGACTTCCGATATATTTTGAGCAGTTGAGGCTGTGATAATTGTATCAGTAAGGGGTTTTGGGTTCAAATGGTAAAAACTAGCTGTCACCATCATAAGCAGATAACATACTTAATGATATGGATTAGCTCATATAATCAAGGAAACAGCTGAAGAACCAGATGTAGAAAGGACAGGACTCAGAAAACCTAGGGATTTAGATAGGAAGAAGTATTTGGCAATGTCATCAGCATTCATTCTACTAAACCCATTTTTGTTTTTTCTCTGACTCCCAAGGTTTGCAGCCATGGGCAAGAGAAATTGGCCTGGCTTTGACCATGAGCCATTCCCTTGGTTTGGGCAGGGCAGACACTCTGATTGACAATCCTACCAGCACTGCACACAACAGCAGAGAAGTAATTCCCCAAAGGGAGGAAAGAGAAAGGAATGTTGAGAAGACATCAGACTAGAAAGAAGCAATGTGATCACATCTTACTAGAAAAATGCCTCTGGTGGCAGTGGGAGGATGAAATAGAAGAGATCTGGGTTGAACATACATGACTGATTTGTGTCAGGTTCTGAAAGAGAACTATGGAATGTGTAAATGATGTCATCATACAGACGTGCTTAGAGCTCTTCAGTGGAAAGGCTGTATCGATGTCATTTGTTTAGCGAGTAATCATCAAATGTCTGCCATGTGCCGGCAGCTATGAAGGCAGTAAACAGACAAGGTCTCTGCCCTTCAGGACCTTAACATTTTGTTGGGGGAGATAGATAGTAAATAAATATGCAGTGTGTTGGATGGTGATGAATTCTTGAAAAATAAAGGAGTAAGGGTGATATCCACAGTGGAGGGCAGGGTGTTGTTTTCTGTGGGGTGGTCTGGGAGACCTCTGCTTAGATGACATTATCTAAAAGAATAGAAATTTGTTTGTTTTTATCTTTTAAAATCTCAAAGAAGGGAGTGCATGTTCAGGGCAACTTGAATCTATGCTCTTGGGTTACCCGCCCCCCCCAAAAAAAACACCTCAAAGAAATACAAGCTGTGATAGATAACAACGTTAAGAAAAAAATGTTTTTATAG
Seq C2 exon
CCTAGGATGTGGCATTGGATATGGTTATTTGCATCGAATACCTACACGCCCATTTGAGGAAGGAAAGAAAATTTCTCTTCCAGGACAAATGGCTGGTACACCTATTACACCTCTTAAAGATGGGTTTACAGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000115806:ENST00000234160:5
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.030 A=NA C2=0.444
Domain overlap (PFAM):

C1:
PF044959=GRASP55_65=FE(31.4=100)
A:
NA
C2:
PF044959=GRASP55_65=PD(11.7=35.6)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping 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