Special

HsaINT0070575 @ hg19

Intron Retention

Gene
ENSG00000155265 | GOLGA7B
Description
golgin A7 family, member B [Source:HGNC Symbol;Acc:31668]
Coordinates
chr10:99623687-99624026:+
Coord C1 exon
chr10:99623687-99623839
Coord A exon
chr10:99623840-99623924
Coord C2 exon
chr10:99623925-99624026
Length
85 bp
Sequences
Splice sites
5' ss Seq
AAGGTGGCC
5' ss Score
3.58
3' ss Seq
TCTGGCTCCTCTTTTTGCAGGTT
3' ss Score
10.98
Exon sequences
Seq C1 exon
ATCGAGCGGCAGCTCTTTGAAGAGACTGTGAAGACCCTCAACGGATTTTACGCAGAGGCTGAGAAGATTGGGGGCAGCTCCTACCTCGAGGGCTGCCTGGCCTGCGCCACGGCCTACTTCATCTTCCTCTGCATGGAGACCCACTATGAGAAG
Seq A exon
GTGGCCCCTCCCGCCCCACCGTGCATCCCTTCCCTCAGGGCTGCCCTGTGGCATGCTCATCCTTGTCTGGCTCCTCTTTTTGCAG
Seq C2 exon
GTTCTCAAGAAGATTTCCCGCTACATCCAGGAGCAGAATGAGAAGATCTTTGCACCTCGAGGCCTCCTACTTACAGACCCTGTGGAGCGTGGGATGAGGGTT
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000155265-GOLGA7B:NM_001010917:3
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:
PF102564=Erf4=FE(43.5=100)
A:
NA
C2:
PF102564=Erf4=FE(28.7=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
ACGGATTTTACGCAGAGGCTG
R:
GCCTCGAGGTGCAAAGATCTT
Band lengths:
176-261
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