Special

HsaINT0151624 @ hg38

Intron Retention

Gene
ENSG00000115840 | SLC25A12
Description
solute carrier family 25 member 12 [Source:HGNC Symbol;Acc:HGNC:10982]
Coordinates
chr2:171813339-171815202:-
Coord C1 exon
chr2:171815121-171815202
Coord A exon
chr2:171813498-171815120
Coord C2 exon
chr2:171813339-171813497
Length
1623 bp
Sequences
Splice sites
5' ss Seq
GAGGTGAGT
5' ss Score
10.03
3' ss Seq
AAAAATTGTTCTGTTTGTAGCTG
3' ss Score
6.44
Exon sequences
Seq C1 exon
CAGTCTCCTGGGTTAGGCAGGCCTATCTGGCTCCAGATTGCCGAGTCTGCTTACAGATTCACTCTGGGCTCAGTTGCTGGAG
Seq A exon
GTGAGTGACATGTCTGTGTGCTGTTTGAGGCTTGTGTTAATGTAATATTATCTCACCAGACTGAGGCAGATCAGCAAAGGTGCAGTTCATTGTTCCCATGGGTCACGACTTCAGGGCTTTCTGAAGTGTTCTTTATTTTTACCTATGATCAGGAGACTTGTCGTAGCAATGGCTATGACCATCTGGCTCCAGTCTGTCTTCAGGACAGAACCTCTGTAATGATGTGAAAGTCTGGGATGCAGTGCTGCACTCACCTTAATTATACTGGCTAAGGCCAGTATGAAAAAATGGAAAATGAGACTGTGTTTATGGGACAGGTTAAGAAATTGAGATTCGCTATTATCCTTAGCAAACTAACGCAGGAACAGAAAACCAAATACCACATGTTCTCATTTATAAGTGGGAACTAAATAGGAGCTTATTATGAACACAAAGAAGGAAACAACAGACACTGGGGTCTACTTGTGGGGGAGGGTGGCAGGAAGGAGGGGAGCAGAAAAAATGACTGTTGGATGCTGGGATTAATACCTGGGCGATGAAATATGTACAACAAACGCCCGTGACACGTGTTTACCTATGTGACAAACCTTCATATATACCCCACACCTAAAATAAAACTAAAAAAAAAAAGAAAGAAATTGAGATTTGGGATATGAATCCCAGAACCTCGTGAAATAAAAGAGCCTCTCAAAGTGACCCAGTTTTGCTTTTCTGCTTGTATGTTTTCCTTTCCCTTATCGCTTGCTTAACAATATCTGGACTTGATGTTTATTTGCAAAAATGAACCTCCCTTCCCTCCCTGTTCACAGCCAAAATTTGAGAGACTGTTTTTGCTTAAATACTCTACTTAGAAAATGTGTACAATCTGAAGTTGCTTTGTTGAGAAGAAGCTAGCAGGTGTGATTAAAATGCTTACGATTTTTTAAGATAAGCCTGAACTCAAAAGACTTTTTTTTTTCTTTTCACTCTCAGTTTTAGAAGTTGCAAACCAGGTTTTGGCTTTCAGCAGTCAAAATGTGTAATACTCTCGTTCATGTAAATAAATTTTCATTCCCTGAGAAATTCTAAAGCATAGCCATATTTTCTTTTAAACCAAATTCTATACATAGGGATAGGATAATGTTGAAGTGTGTTTCTAATATTATGGTTGTAACTATGATTAATTTACCAAGATGCTTTATTAAACTAAATTTTAAAATCGTAGCCACCTAGTGTACGGATATAGTCATTTTAAGAAGTAACTGGCATAATATTTAAGCATTTAATGGAAAATATAAATAAATGTTATACATAATAGTTTAATGTTGTTACTATAGAAAACTGAGTGTTGATTATCTAATTTGGGAAGTGACTCGATAATCCACTCTGTAGTTTATGAACCTACGATATCAAAGAGCATTCTTGACAGTTGTTTTCTGAAGCAGCTGTATTTATGGATTTCAGTGCTTGCTATAGCCTGCTATCCCTAAGGTGTTTGTGAGGGAAAGAAAAATAATAAACTCTCTTTTGTGAGAATACATGTTGTGTTTTATTTTCTCATCCTTTAAGATAAGATTTGTCATCCTTATGGACTCTCCATTTAATTGTGTTCTTTTTTAAGCCTAAAAATTGTTCTGTTTGTAG
Seq C2 exon
CTGTGGGAGCCACTGCAGTGTATCCTATAGATCTGGTGAAGACCCGAATGCAAAACCAGCGTGGCTCTGGCTCTGTTGTTGGGGAGCTAATGTACAAAAACAGCTTTGACTGTTTTAAGAAAGTCTTGCGTTATGAGGGCTTCTTTGGACTCTACAGGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000115840:ENST00000422440:10
Average complexity
IR
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:
PF0015322=Mito_carr=PU(14.3=50.0)
A:
NA
C2:
PF0015322=Mito_carr=FE(54.1=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:
CAGTCTCCTGGGTTAGGCAGG
R:
CCTGTAGAGTCCAAAGAAGCCC
Band lengths:
240-1863
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains