Special

HsaINT0151759 @ hg19

Intron Retention

Gene
ENSG00000148339 | SLC25A25
Description
solute carrier family 25 (mitochondrial carrier; phosphate carrier), member 25 [Source:HGNC Symbol;Acc:20663]
Coordinates
chr9:130864649-130866118:+
Coord C1 exon
chr9:130864649-130864760
Coord A exon
chr9:130864761-130865959
Coord C2 exon
chr9:130865960-130866118
Length
1199 bp
Sequences
Splice sites
5' ss Seq
ACGGTGAGC
5' ss Score
9.44
3' ss Seq
TGTGCCATCTTTCCTCACAGATC
3' ss Score
12.09
Exon sequences
Seq C1 exon
CATGGATAAAAACGGCACGATGACCATTGACTGGAACGAGTGGAGAGACTACCACCTCCTCCACCCCGTGGAAAACATCCCCGAGATCATCCTCTACTGGAAGCATTCCACG
Seq A exon
GTGAGCCCCACGTGCCCAGGGCCCTCATCTGCTCCCAGGGACCCTTAGCCCAGAGTCACCCAGTCGTCCCCATCCCAGAGTGCAGCTGGGGCTTTCCAGCCACCTCCTCTTCCACAGGAGACTGTCCCCTCTTCTGCCAGCCCAGTAGAGCTGTCCGCATGTTCCCCATGTTCTGGCACTCCAGCCAACCTGAACAGCCCCATCGTTCACACACACAGGCTTCCTCTTCCAGGAACACCCTCCGTCCCCACATGCTCCCTGCTCCCTGCTCCTCATGGGCCACTTCAAATACCCCTTCCCATGATGCTGTCTGTTCTCCCAAAGCTGGTATGAGCCTTCCCCCCGGTGGGAGGGGGCTGGGGCAGAAGCTACTCTACAGAGAACACCTAGGCAGAGCTGTGAGGTGTCCCCACGGTCACACATTTGCTGCCCTCTCGCCCCCGTCCACTGTGGTTTCATGTTCAGAAATGTGAGTCTGTGCTGGTCTCTGCCCCGAGCCCTTCATGCTTGGCGTGTCCCTCTCTGAGTCCTGGTGTGCAGTCCTGTCCCTCTGGACCATCCGCTCCAGGAGGGGAGGCCAGAGGCGCTCCTCATCTGCCTCTCGCAGTGCCAGGCCAGGGCTTGTTAGGTGAGATTAAATGGACAGCTCCAGGGGTGGGAGTAGCTGGCCCAGAGCTCTGGCCTTTAGCCCTGGGATCAGAGCAGAGGTGGCTCTGATCAGCCCGGATGTCACCCGGAGAAAGGTTACGCAGGCAGCGAGCCCTCGTGTTTGCTGAGGCGTTGCATAATGTTCTGCCAGCGTGATCTGGTTACACGTGAGATCTCAGACGGCTCTCACCCCGGCCTGATCCCTTCAGCGCAGCCAGCCTGGCAATCTCACACAGGCCTGTGAGCTGTTCTTGCAGTAGCTCCCTGGCAGCATTGGAAAGGGCCGGTGAATGGTTTTCTAACCGGCACCTCCCGGCTGTGTTCAGCTGAGGTTCTATACCTGTGCCTCTCCAGGACCCCAGCAGGGGTGAGAGCTCTGCTACCTTCAGAGTGAAGGGAAAGACCCCAGCCCGCTTCCCACCCAGAGTCCTTGGCCTTCTCCCTGTCCTGTGGTCCCTGGCCTGGAGCCGTGCTAGAGGGTAGACGGCGACAGGTGCCAGCAGCCTTGCCCCAAGGGTCCTGAGTCAGGCTTGTGCCATCTTTCCTCACAG
Seq C2 exon
ATCTTTGATGTGGGTGAGAATCTAACGGTCCCGGATGAGTTCACAGTGGAGGAGAGGCAGACGGGGATGTGGTGGAGACACCTGGTGGCAGGAGGTGGGGCAGGGGCCGTATCCAGAACCTGCACGGCCCCCCTGGACAGGCTCAAGGTGCTCATGCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000148339-SLC25A25:NM_001006643:4
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.004 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF0003627=EF-hand_1=PD(68.0=44.7)
A:
NA
C2:
PF0015322=Mito_carr=PU(35.1=62.3)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GGCACGATGACCATTGACTG
R:
CATGAGCACCTTGAGCCTGTC
Band lengths:
255-1454
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains