Special

HsaINT0067766 @ hg19

Intron Retention

Gene
ENSG00000136895 | GARNL3
Description
GTPase activating Rap/RanGAP domain-like 3 [Source:HGNC Symbol;Acc:25425]
Coordinates
chr9:130147306-130149610:+
Coord C1 exon
chr9:130147306-130147424
Coord A exon
chr9:130147425-130149471
Coord C2 exon
chr9:130149472-130149610
Length
2047 bp
Sequences
Splice sites
5' ss Seq
AGGGTGAGT
5' ss Score
9.25
3' ss Seq
TGCTCTCTCTTCCTTTCTAGTCG
3' ss Score
10.88
Exon sequences
Seq C1 exon
TCTGTGCTTTCCCGTATCTCCTGGCCTTCACCACCGACTCCATGGAGATCCGCCTGGTGGTGAACGGGAACCTGGTCCACACTGCAGTCGTGCCGCAGCTGCAGCTGGTGGCCTCCAGG
Seq A exon
GTGAGTAGGACTGGGATTTTATCTCTGAGTGGTTTGGGGGACCCCGGCACTGTGGGATTTCAGGTGAGCACAGAAGCCGCCTCTTGTCAAGTTAGGCTGATGAAGACCGGTGTCAGAATGCCAGCACGAGATGGAAAGCCTGAAACCAGACTGATCTGTTGGGTTTTCATGTGTGATTTCTGTGGGCTTTCAGAACACTCCTCAGCTTTGTTAATAGTCATTAACTGGTGCTGGTGGCAGCTGGGGAGCACTTAGCTGAAAAGAGATATCCCCGCTCAGAGACTGGGTCAGTTATTCATGTCACTGCTGCCCTGGAGGACAGTCCAAGTCTAGAAAAGTCAGAGCTTGCAATCTTTCTTCCTTTCCCACCCTCTATCCTCAGTTTGAATTCTTAGCCTATGAAACATGGCTAATTGATTAATCCCTGCCTCATAACCCACAGCTAGGGCAAAACGGAGGGATGCAGGAACAAAGATGCCTTCCAAGATGTCTTTTGTCGCTGGCATATAATCTGGGGGGTCTTGTTCTAGTCCCCTCCCCTGAGTCAGGCCCACAAAGTCCTCCCCAGCCCTGCCAGACTGGGCTGGCTCCCCCGCTGTGTCCCCTGTTCCCTTCCCTGGTCCTGACATCCATCACATTTGGTGGTAGGTGACTGCCTATTTGTTCATCTTTGCTGCTGCACTGATGGTTCTGTGAGAGCAGATGCCATGCTGTCTTACCATCATAGTACCAGTGGTGTGCTCAATGCTTCAGTCCCGCAGTGCTCTGGAAAATGTGTGTGTGTGCACATATGTGCATATATGTATGATATGTGTACATATCTGCATGTATGTATCATATGCGTGTACATTAGTTGATTGTAAATAGCTTACAATTTACAAATAATAAATATACAATGCTGTTTATCATAAAAATCCACTTAGCCAATTGGTTCTTACAAAATGTTTTTGTTAATATTTGCTGAACTCTTGTATCCATAGCCAACCTACAGTTGCAGTTCAACCATGATTTTACACTTGGAGTTATATCTCAATCCACTCATTTTTTTCCAATGTATATTGTCATTTAATCTGATAGGTAATCTGCTATAAAACTATTTTTCACCCTCATACAACTCATAGTCATTAAACTGAAACTTCTTTCAGCTTCTGTACCAGACTAAACACACTTCTACGTTTCTTGTTCATTACTAGTACTTTCTCCATCACTGTAAGTCTAGACAATCAACAAAACAACAAATCAAAGTCAAACTGATAGTCTTTGCTGGATTCCATGGTGTAAAGAGTCCCTGCATGATTGATTTCAAGCTGCCAGCGTGACGCCACTGCAGGTGGTGCTGGGGAGACGTGCATTATCCCCCATGGTGCAGTATCTCTCCCCCAAGCCCCACACAGACACTGTTGGTGTCAATAACTCCAGAGCAGATGTAATAGTAAGCACAGTCAAATAATTAGGAATGGCTGGATTTGGATATTTAGGGCCTTTGTTTTTTTAGGTTTGTATAATTTAATTTCTAATCATGTGTGTTTAACAGCCAGTTTGCAAAATTCCTGAAAATTGGATTTCATAGATCACATCCAGCACACCACTGCTGTTAGCAGCAGCGCCAGCGCATCACGGGTGTGCCTGAGTATCTGCTGGATCAGTGAATGAAGAATCCATTTCCCCATCTGCCAAATGGGCCTAACTGAATCCCTAAGATCTTTCCCGTTCTAACACTCCAGGTGCCTGAGATTCCTGTTAGGGAAGTGTGTGCTGTGTTTGTGATTGCAGAAGATGTGTGGTGGAACACTGACTGTTTTCTATTGTGGATCAACAAATAGATGATGAAAAGTGGCGGGGAGTGGAATACTCAGGAAAAGTGTAACTAGCCACGCTGGGCTTTCCTCCAGAAGGCTCTCTCCATCCCTCGCCCCGGCATCCCGCACTGCACTGTATGCTCCAAGGATGGGGACCAGTTGGAGGGTTTGCAGTGATGGCAGGAGGGCCAGTGGATGCAAGGCCTAGAACACCAGGCAGCCCGGTAATGCTCTCTCTTCCTTTCTAG
Seq C2 exon
TCGGATATATACTTCACAGCAACTGCAGCTGTGAATGAGGTCTCATCTGGAGGCAGCTCCAAGGGGGCCAGTGCCCGAAATTCTCCTCAGACACCCCCGGGCCGAGATACTCCAGTATTTCCTTCTTCCCTGGGGGAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000136895-GARNL3:NM_032293:24
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.000 A=NA C2=0.574
Domain overlap (PFAM):

C1:
PF0078017=CNH=FE(12.8=100)
A:
NA
C2:
PF0078017=CNH=PD(0.1=0.0)


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

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