Special

HsaINT0136882 @ hg38

Intron Retention

Gene
ENSG00000017797 | RALBP1
Description
ralA binding protein 1 [Source:HGNC Symbol;Acc:HGNC:9841]
Coordinates
chr18:9522160-9524755:+
Coord C1 exon
chr18:9522160-9522509
Coord A exon
chr18:9522510-9524593
Coord C2 exon
chr18:9524594-9524755
Length
2084 bp
Sequences
Splice sites
5' ss Seq
CAGGTACAT
5' ss Score
7.79
3' ss Seq
TGTAAATCTTTTTTTCTTAGATC
3' ss Score
8.22
Exon sequences
Seq C1 exon
GAATTAAATCAAAGGTGGATGAGCTAAAAGCAGCCTATGACCGGGAGGAGTCTACAAACTTGGAAGACTATGAGCCTAACACTGTAGCCAGTTTGCTGAAGCAGTATTTGCGAGACCTTCCAGAGAATTTGCTTACCAAAGAGCTTATGCCCAGATTTGAAGAGGCTTGTGGGAGGACCACGGAGACTGAGAAAGTGCAGGAATTCCAGCGTTTACTCAAAGAACTGCCAGAATGTAACTATCTTCTGATTTCTTGGCTCATTGTGCACATGGACCATGTCATTGCAAAGGAACTGGAAACAAAAATGAATATACAGAACATTTCTATAGTGCTCAGCCCAACTGTGCAG
Seq A exon
GTACATGGTCTTCTCTACACATATACCCTCTGGTACTGACATTGGGGAACTGGGGTAATTTTCTATTGCTGAGTCACATGTAAAGCAGTGAACTTGAGGAGATAGGTAATGGATTAGCTTGAATACGGGTCTTTTCCTTTCATAATTTGGACAGTGTCAATGTATAAGATAACATACTTGCCCTTTAGCTTGTAGTGATGTAATTTGAATGCGGTACAGTCTTTGATGTGGGTTTATAAACAAGACCTGATGACAAGGATCCTTCATTAGGGGAGGAGGAGCCCATGGCATCTACAGTTATAGAGTTCGTGTGTAGAATTTTAGAGATCCCAGTTATTTAATCAATAGCATTATTGCTTCGTTAGATCACAGACACACATCAAACTCAGGCACAAAGGGACCTGTCATTAATTGTTTGGTCAAAGATTTAGCCTGAGGATTTCATTCATAAGGATGGATCCTAGAGAGACATGTTATAGGCTCTGAATCTGAAAAGGAACTTCAGGGAATTGGGTAGTGTGTTAATTGGTATCTTTTTACGACATACATACTTGGCTTTCCTTTATTGCTGCTCAGTTGGTGCTGTCATAGAGTATATGTTTTCTTTTAATTGCAGTTAATGATATTTTACTCAGGCCAATAAAAAGGGAGATGATAGGTTATATTTATTATCTTAAGCCCTCTTTTTGGCCAGTATTCTGAGTCACCATAAATCACTGTCACTGTTATTAGAGAGTGTTTTCATTTACTAAAGAGCGTTTCAGTCAGGCGCGGTGGCTCACACCTTTAATGCGAGCACTTTAGGAGGCTGTGGCAGGAGGATAGCGAGAGGCCAGGAGTTCAGCCTAGGCAACATAGCAAGACCCTGTCTCTACATAAAAATTAAAAATTAGCTGGGTGTGGTAGCATGTATGTGTAGTCCCAGTTACTTCGGAGGCTGAGGTAGGAGGATTGCTTGAGCCCAGCAGTGAGCTATGATCATGCCACTGTACTCCTCTCTGGGTGACAGAGCAAGATTTTATCTCTAAAAAATAAAGATTCTTCTGTTACTCATTGATTACGCTTTGAAAGCAAAATGTTTCTCAGATTTTAGTTTGATCATTAGGATTTCAGGATCTGGTAAATATTACATTGATACTTAATATTACTATAATATAATAGAGATGGTTGTATCATAGAAGAGTCAAGTGTGTTGTAAGAGTAAGTTTTAGGTAGGAAATAATTTCTTGTAGTAGCTTTTCAGCCAACCTAATGCCCTGGCCTCCTAGCATATGAACATCCATACTTAAATGCTGGCTGTGTCCAGGTATTTGTTTCTGGAGTGAGGGCTTTCAACCTCAACCCAGCTTTACTACTGTGGTGCTCCCACTTCCCTCATGGTCCTCATTCATTCCATTGCGTCTGTTAAAATATGTCAAAGTAAGTTGAAAATAAAGAATATAAGATGTTTTAGCCGGGCATGGTGGCTCACGCCTGTAATCGCAGCACTTTGGGAGGCTGAGGTGGGTAGATCATTTGAGGTCAGCAGTTCGAGCCCAGCCTGGCCAACATGGTGAAACTCCGTCTCTACTGAAAATACAAAAAAATCAGCCAGGTATGGTGGCACACGCCTGTAATCCCAGCTTACCGGGGAGGCTGAGGCAGGAAAATCGCTTGAACCCGTGAGGTGGAGGTTGCAGTGAGCTGAGATTGTGCCACTGCACTCTAGCCTGGGCTACAGAGCGAGGCTCCATCTCAAAAAAGCACCACCACCGCCACCAACAACAAAAAACACACAAAAAATAAGATGTTTAAATCAGTTAATACTGTGATAGAAAAAATAAACAAATGGATGGCATCAACTTCTCTATCCTTTTCTTGACTTTTTTTCCCTTCAGATCTTTCTGGTGCTTGAATACATGATTTAACTCATATTTTACCATTTTCTTCTTAAATTGGCTATTAACTAGCAAAGACTGTGTTGTCATTACTGGGTAGAATTTTCTTTATGTGTCCAGGATTAAAGGATATATTATGTAATAGACACAAATAAGTGAAATAGAATGATAGTTTTAATGGTTTTCTTGTAAATCTTTTTTTCTTAG
Seq C2 exon
ATCAGCAATCGAGTCCTGTATGTGTTTTTCACACATGTGCAAGAACTCTTTGGAAATGTGGTACTAAAGCAAGTGATGAAACCTCTGCGATGGTCTAACATGGCCACGATGCCCACGCTGCCAGAGACCCAGGCGGGCATCAAGGAGGAGATCAGGAGACAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000017797:ENST00000019317:4
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.017 A=NA C2=0.074
Domain overlap (PFAM):

C1:
PF0062022=RhoGAP=FE(79.5=100)
A:
NA
C2:
PF0062022=RhoGAP=PD(2.1=5.6)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
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

  • Autistic and control brains
  • Pre-implantation embryo development