Special

HsaINT0067756 @ hg19

Intron Retention

Gene
ENSG00000136895 | GARNL3
Description
GTPase activating Rap/RanGAP domain-like 3 [Source:HGNC Symbol;Acc:25425]
Coordinates
chr9:130106514-130107756:+
Coord C1 exon
chr9:130106514-130106618
Coord A exon
chr9:130106619-130107681
Coord C2 exon
chr9:130107682-130107756
Length
1063 bp
Sequences
Splice sites
5' ss Seq
CAGGTGGGT
5' ss Score
8.56
3' ss Seq
AGAGATCTCTGTTCTGTAAGGCA
3' ss Score
-0.24
Exon sequences
Seq C1 exon
AACATGCTTAATAGACGATCTTTTAGTGATGTCTTACCAGAGTCACCCAAGTCAGCGCGGAAGAAAGAGGAGGCCCGCCAGGCGGAGTTTGTTAGAATAGGGCAG
Seq A exon
GTGGGTTTTCTTCTGAAACCTTTTCTGCGAGACATGTAGTTTTGAGTTCCATCCTAACCAGATGGCCCATGTGCAAAGACTTTGTTTGCCTGCTGCTGTAGGAGCTCTGTAATTTCTGTTAGGATTGTTGTGGCAACCACGAGTGAGATTTTTGAGAACCGAGTAGGTGCAGTTCTCTGCAGGCATCACTGAGAGAGCAACACTCTGCAGAGGTAGGAATGCTACTGCCTCAAGGCAAGTAGCCACAGGGCCCAGCTCTGGGCCCCCCTCTTCCAGAGAACACAGATCTCTTGCCTGCCTCCTAGGAATTTTCTGAAGAGTGAGGAGCCGATTTGGGAAATGCCCCTTAAACCCATGACTGGCAGGAGGAAGCACAGAGTGGCAGTGGCACTCACAGAAGACTTGAATTACCACCCTATGACTTGGAAACAATCCAAGTCACCACCAAGTTAGGTGGTGCCCAGTCATCCCCTTATTCCAGGCATTGGAGAAAATCACTCCCTTTGCCCCGCTCGCATGTGACACTGGTATTTCTCAGTTCCGGGAGGCGACACAGCTGTCTGCCTTGATCACACATCACAGCATGGAGAAGGAGGAGTGCCCTCAGCTGCAAATAAGGTTCTGGCCCAGAAGTAGAAAGCTAGACAAGGCAGGTGGAGAGAGGAAAGCCATGTAATCAAGGGAAGCTTAGTTACAAGGTTCTCAAACATTGGTTCTTGTTTAAAGATACCCAGACTTTATTCCCAGAGATTCTGATTCATCAAGTTTGAGGAGGGACCTGAGAATCTGCATTTTTTCAAGCTCATGGTTTATAAATCACAGTAATGATATATTGATTCATTGAAATGATAAAATGCATTTGGATAATTTGGGTTGCGACATTGTCATTAAGGCTTCACTGTGTCCAGCTAACTTCAATTCTTGATTAACAAGTCAGTAGAGGAACCCGAAATGTTAGCCTGCAATTACTCCTGTTTTATTAAATTTTTGTCAAATCACAATTGTTTATCCTGCTGTACTTTTGCCGCCTAGTAAACTTTAATAGAGATCTCTGTTCTGTAAG
Seq C2 exon
GCACTAAAACTGAAATCCATTGTGAGAGGGGATGCTCCATCAAGCTTGGCAGCTTCAGGGATCTGTAAAAAAGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000136895-GARNL3:NM_032293:15
Average complexity
IR-C
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.343 A=NA C2=0.000
Domain overlap (PFAM):

C1:
NO
A:
NA
C2:
NO


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

  • Genotype-Tissue Expression Project (GTEx)
  • Autistic and control brains
  • Pre-implantation embryo development