Special

HsaINT0137390 @ hg19

Intron Retention

Gene
ENSG00000091428 | RAPGEF4
Description
Rap guanine nucleotide exchange factor (GEF) 4 [Source:HGNC Symbol;Acc:16626]
Coordinates
chr2:173852924-173853567:+
Coord C1 exon
chr2:173852924-173853000
Coord A exon
chr2:173853001-173853420
Coord C2 exon
chr2:173853421-173853567
Length
420 bp
Sequences
Splice sites
5' ss Seq
AAGGTATAT
5' ss Score
7.84
3' ss Seq
GTGTGCTCTACTCTATCCAGGGT
3' ss Score
7.66
Exon sequences
Seq C1 exon
TGTTTAACCAGGGGGAAGAAGGTACCTCCTGGTACATTATTCTAAAAGGATCAGTGAATGTAGTCATTTACGGCAAG
Seq A exon
GTATATATATCTTTTTCTTTTTGAAACTTTATTACGCTCCACTTACTAGTGTGGCTCTAAGTATTAGCAATGTAGTGCCACAATTAAATTTGCAACAACATTGCTCCTAGATGTAGAAAAGACATTATTGTATCTTTAATCATAAGTTACCTCAGTTATTATACTTAAAGTTGTATTGTACTTTCTGGGGTTTGTCTCCTGATGGATTATAGTGTGTACATTTAAGTTAAGCCACAGACCGTATTACTCAGTGAAAGCAAAGTGAACATCATAATGTAATTATGTAATCCCCTTTGGCATCGCTAGGTACAGCCCATTTATCTACAATGTTTTAGGGGCTTGGGGGTCTTGTGGCAGGAGGTGGTGGGTGTTTGCTCTATTTCAGGGATCTTCTTCATCTGTGTGCTCTACTCTATCCAG
Seq C2 exon
GGTGTGGTCTGCACCCTGCATGAAGGAGATGACTTCGGCAAGTTAGCACTAGTGAATGATGCCCCACGAGCTGCCTCTATCGTCTTACGAGAAGATAACTGCCATTTCTTAAGAGTAGACAAGGAGGATTTCAACCGGATCCTAAGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000091428-RAPGEF4:NM_007023:13
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:
PF0002724=cNMP_binding=FE(28.7=100)
A:
NA
C2:
PF0002724=cNMP_binding=FE(55.2=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
TGTTTAACCAGGGGGAAGAAGG
R:
TTAGGATCCGGTTGAAATCCTCCT
Band lengths:
222-642
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