Special

HsaINT0137475 @ hg19

Intron Retention

Gene
ENSG00000108352 | RAPGEFL1
Description
Rap guanine nucleotide exchange factor (GEF)-like 1 [Source:HGNC Symbol;Acc:17428]
Coordinates
chr17:38348465-38348945:+
Coord C1 exon
chr17:38348465-38348515
Coord A exon
chr17:38348516-38348857
Coord C2 exon
chr17:38348858-38348945
Length
342 bp
Sequences
Splice sites
5' ss Seq
ACGGTGAGT
5' ss Score
11.45
3' ss Seq
TCTCTCCTGTGGAATACTAGGAC
3' ss Score
5.62
Exon sequences
Seq C1 exon
AAGCTGCCAGGGAAATTCAAGAACTTGTTTCGCAAATTTGAGAACCTGACG
Seq A exon
GTGAGTGGGTTTGGCTCTTTCTTCTGCTCTTGGACTGAGAGCCCAGAAACCCTCTGTTCCCATAAACCCCCTTCCTCAAGCTTTCCTTTCAAGGTGTTTAGTGTATGGGACCCCCCACCCTCCTTACCATGCTGGAGGGTGAGGTTGGAAGGATTGCGCCCCTGTTTTTCTTGAAGGAAAGGGGGAGTAGTCAGGTCCCTCCCCACCACACCATTAGAAAGCCCCCAGCACCCCTATCTGATCAGGAATGTATACAAGGCAGGGGGTGAGGGAGGAAGCTGAGGACATCTTTGGGATGCATTGGCCAGTCTGTCCCTTGATCTCTCTCCTGTGGAATACTAG
Seq C2 exon
GACCCCTGCAGGAACCACAAAAGCTACCGAGAAGTGATCTCCAAAATGAAGCCCCCTGTGATTCCCTTCGTGCCTCTGATCCTCAAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000108352-RAPGEFL1:NM_016339:11
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=0.000
Domain overlap (PFAM):

C1:
PF0061714=RasGEF=FE(8.6=100)
A:
NA
C2:
PF0061714=RasGEF=FE(15.7=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
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