Special

HsaINT0073581 @ hg19

Intron Retention

Gene
Description
gametocyte specific factor 1 [Source:HGNC Symbol;Acc:26565]
Coordinates
chr12:54855893-54856509:-
Coord C1 exon
chr12:54856426-54856509
Coord A exon
chr12:54855957-54856425
Coord C2 exon
chr12:54855893-54855956
Length
469 bp
Sequences
Splice sites
5' ss Seq
AAGGTGAGC
5' ss Score
9.6
3' ss Seq
TGTTTTGCTTCCTTTAACAGATT
3' ss Score
11.18
Exon sequences
Seq C1 exon
TCAACCAAACCAGGAGCCTTAGACAAGAGACTCTGGCTGAGAGCACTTGGCAGTGCCCTCCTTGCGATGAAGACTGGGATAAAG
Seq A exon
GTGAGCTGCCTCTACATCTTTTTCTTCACAATGTCTAAATCTCAAGTCATTTGCTTAAGACAGAAGGAAGATTTTCCTTTTTTATGAACATACCATGTTGTTCAGAATGCCTTATTATTTTTATTGGGCCCCAAAACGAGCACATTTGTATCGCTGTGCAGACACGTGGAACAGCCAATCCCTCTTGATTGGAAAAAGCACTTCTTTACATCTGTTTTTTTCCATAAATTGTGTTGTACCATCTGTGTTTGATTGTTAGTAGGCACGTTTATTATTATTTATGTTGCTTGTGTTTATATTCTTCAATTAAATTCTTGCTACTGTGTCACTTAGGCAGGACACTTGATCAATTTTTACTTGCTTCTGCAAAACTTAGGTGTATTATTTCCCATCTTATAAATTCAACCAACATGAACTGCTGGTGTCTTATCTAGTAGTACCACAAACTATGTTTTGCTTCCTTTAACAG
Seq C2 exon
ATTTGTGGGAGCAGACCAGCACCCCATTTGTCTGGGGCACAACTCACTACTCTGACAACAACAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000170627-GTSF1:NM_144594:5
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.138 A=NA C2=0.227
Domain overlap (PFAM):

C1:
NO
A:
NA
C2:
NO


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