Special

HsaINT0151757 @ hg38

Intron Retention

Gene
ENSG00000148339 | SLC25A25
Description
solute carrier family 25 member 25 [Source:HGNC Symbol;Acc:HGNC:20663]
Coordinates
chr9:128101096-128101396:+
Coord C1 exon
chr9:128101096-128101222
Coord A exon
chr9:128101223-128101308
Coord C2 exon
chr9:128101309-128101396
Length
86 bp
Sequences
Splice sites
5' ss Seq
ATGGTAAGT
5' ss Score
11.01
3' ss Seq
CACGGCCTCTGTTCTTGCAGGAC
3' ss Score
10.96
Exon sequences
Seq C1 exon
AAAATTGTACAAGCTGGAGATAAGGACCTTGATGGGCAGCTAGACTTTGAAGAATTTGTCCATTATCTCCAAGATCATGAGAAGAAGCTGAGGCTGGTGTTTAAGAGTTTGGACAAAAAGAATGATG
Seq A exon
GTAAGTGTTGCCTTCAGAGCTGTGGCCGGTCCAGCCTCGGGCCTCCCCGTGCGCCTGGCTCCTGCTCACGGCCTCTGTTCTTGCAG
Seq C2 exon
GACGCATTGACGCGCAGGAGATCATGCAGTCCCTGCGGGACTTGGGAGTCAAGATATCTGAACAGCAGGCAGAAAAAATTCTCAAGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000148339:ENST00000373066:2
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.019 A=NA C2=0.007
Domain overlap (PFAM):

C1:
PF0003627=EF-hand_1=PD(92.6=58.1),PF134991=EF-hand_7=PU(28.8=44.2)
A:
NA
C2:
PF134991=EF-hand_7=FE(43.9=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:
ACCTTGATGGGCAGCTAGACT
R:
TTTTTCTGCCTGCTGTTCAGA
Band lengths:
179-265
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains