Special

HsaINT0151631 @ hg38

Intron Retention

Gene
ENSG00000115840 | SLC25A12
Description
solute carrier family 25 member 12 [Source:HGNC Symbol;Acc:HGNC:10982]
Coordinates
chr2:171784370-171787661:-
Coord C1 exon
chr2:171787571-171787661
Coord A exon
chr2:171785476-171787570
Coord C2 exon
chr2:171784370-171785475
Length
2095 bp
Sequences
Splice sites
5' ss Seq
CCTGTAAGT
5' ss Score
7.52
3' ss Seq
GGCTTTTTTTCTGTCAACAGCAA
3' ss Score
7.97
Exon sequences
Seq C1 exon
CTCGAGTGTTTCGATCCTCTCCCCAGTTTGGTGTTACCTTGGTCACTTATGAACTTCTCCAGCGGTGGTTTTACATTGATTTTGGAGGCCT
Seq A exon
GTAAGTCAGCTGCTCAACTCCTTTACAAAGAAATCACTAAGTCCAAAACAAATGTTTGTTCTGTCTACAAAAGCATTGTTGCAACTCTTAGAAAACTGATAAGACAGAACCTTTAAGACCAATGCATTTAAAACAGTGAGCTTAAGAAGCATTTGTGTTAAGCAAGTAAAACTTGACAGAGTGACATCGTACATAATATTAAGCAGCTATTTGGGGGATTTTAGGGAAGCAGCAAATTTTTTTAAAAAAGACAGGATATCCTCTGTTGCCCAGGCTGGAGTGCAGTGGCATGTTCTTGGCTCACCGTAGCCTCAACCTCCCGGGCTCAAGCGATCCTCCCACCTCAGCCTCCTGAGTAGCTGGGACCACAGAGGCATGCCACCACACCCAGCTAATTTTTGTACTTTTTTATAGAGATGGGATCTCACTGTGTTGCCCAGGCTGGTCTCGAACTCCACCAGCCTTGGCCTCCCAAAGTGCTGGGATTACAGACATGAGCTACCGTGCCTAGCCAGGAGGCAGCAGATTAAAATGCTGTGTAAATAATTGTCTTTTTTCACATAAGCAAATACTGAACTTCATGGCGTTCTCATTATGTGGATTTTATTATATGGCCCTTTCACAGAAGTAATGTAAATGTATACCAGTAACACTTTTGTGCATTTTCTTTCAAAGTCCCAAGCCCTTTTGCATCTCTGATATTTCATTATTCACCACAATTTATTATTAGTTAGGTGCAGATGTTCTTGAAGCTAATTTACTGGAAAAACCAATAGGTTTGAAGAGAGATTTTGCCCATGGATATAATCACTAGTGAGCTGTAGGCCAGAAATTGGGCTTCTAAAAGCTTACCACTTGAAGCTTGCACTGAGAAGAAGAATTACAAGTTGAATTTTCTGGGTGGGGAAGTTGTACCCAAAGCAAGCAATTATTAGCTTTTCAGCAGAAGACCAAGTACCATTCCTGAGTCCTCACATCAGAAACCTGTGAACTCCTCTGTGCCCAAAGGCCATATAGGGAATCAGCTGCTGAACCAAGTGGAGGGACCTATGCAAAAAAAGTGAGAACAGCAGTCTTACAGTTGCATTGTAGAAATGTGAGGCTTCAGGCTTTTCCATGCTTCTTTCATCTTCTGTAAAAGAACTAAAGCTATTTCTCTCTCTCTCTTTTTTTTTTTTTTTTTTTTTTAGACGGAGTCTTGCTCTGTCGCCCAGGCTGGAGTGCAGTGGTACGATCTCGGCTCACTGCAACCTCCACCTCCCAGGTTCAAGTGATTCTCCTGCCTCAGCCTCCTGAGAAGCTGGGACTAAGGGCGCCCACCACCGCGCCTGGCTAATTTTTTTTTTTTTTAATATTTTTAGTAGAGACGGGGTCTCACCGTGTTAGCCAGGATAGCCTTGATCTCCTGACCTCATGATCCGCCTGCCTCGGCCTCCCAAAGTTCTGGGATTACAGGCGTGAGCCACCATGCCCGGCCTATCTCTCTTTAAATAATTTAATTGATAATCTTTATGAGTCTACTACATAAAAAGTTAACTTCTAAAGTTATGTCAAAAGAAAAATATATACTTTAAAAATTACTTTCATATGTGCTAAGTGCAGAAAATTTGGAAAACCATAAAGCATAAAAGAAAAAAACCAGCCTGGGTGTGGTGGCTCACACCTCCCAGTGCTCTGGGAGGCCAAGGCAGAAGGATTCCTTAGACCAGAAGTTCGAAACCAGCTTTGGCAACATAGCAAGACCCCATCTTTACAAGAAGAAAAAAGAAAAAAATCATCCATAATCTTACTACCCAGAGAGTCTTCATATTTGAGTGTCTTTTCTTCTGACTTTTTTCCTATGGATTTGTTTATATATGTATGCAAGCATTGGAAATAAGGCCATTTCTCTTGTAAATCAAATATGTAGATAAGTTGCTGTCAAAGCAGCTATAAATCATGACTGTGGTTTCTAGTCATGCAGCACAGATGCCATGGAAATGGTTGAGAGAAACATTCTTCTTTGTGGCACATGGGTCAGACCGAAAATGTCCAGCTGTAAGCTGCGCTCATCCACCTTGAGCATGCTAACCATTGGCTTTTTTTCTGTCAACAG
Seq C2 exon
CAAACCCGCTGGTTCAGAACCAACACCTAAGTCACGCATTGCAGACCTTCCTCCTGCCAACCCTGATCACATCGGTGGATACAGACTCGCCACAGCCACGTTTGCAGGCATCGAAAACAAATTTGGCCTTTATCTCCCGAAATTTAAGTCTCCTAGTGTTGCTGTGGTTCAGCCAAAGGCAGCAGTGGCAGCCACTCAGTGATGAGACAACTGTTGAGTGTGGCAAAATGGCGCCTTGAAGAAAGAGGCCTAGGAGAGCAGCCCTGTAATGTATCCAGTCAGCTGCATGGTACTGACTGAGCTGAGGAGTCAAACTCTTCTTTCTGTATGACATATACATATACTTGTTTATAAAATAATCATTTGCCCAGGGAAAAAACCACAACGCTGTTTCAAGCTTTAGTCTTATGTGTTGAAATGTTTTTGTAAGCCTTGGCATGAATTAGTGTTCTAGACTCTGCTTTGCACAGCTTGCACTTACAGTGATTGTACATATTGTACATCTTTGTACAGAGACATCTTGGCACCTCATCCCAACAAATCACATTTGTAGAAATGTAATGCGGTTCTGAGTGGCTTGAAATGTACAGAATGTTTTGAAAGTGTTTTATTAAGAATCACACAAAAATAAATGTATTAAAATTAAATTCATTCTCTTATTGGTGACTTATGGAAATAAAGCATCAATATTGGATGTATTTAATTCCTAGTTTGTTTTCCATTCTGGAATAAAAAGGTATTTGCTGATAAAAGGCATAACGAGACATAGTGCTGCTACCACTGAATAAGTGATACTTTGGAAAGATGCATGCCAGTGGATGCCAGAGGACCAGGCTAATGACTTGTGTGTGCTGATGTGTTTCCATTTGTATTTAATGTGTGTAGACCCTCCTCTGTTCATCAATCAAAAAGCATTTCCTAGGCAGCTCCTCGCCTGTCAGTGTGCATATGGAAACAGGGACATCTCCATCATTACTGGCTTAGTTTTGCTTTCCTTTGACACAGTAAGGCAAAGGCCAAGCTTTCAAAAGAGTAAAGGATACTTTCACAATTTCCCTTCATATGGATATGATTCCAGTCAAAAATAAAATGCACACCAAAATGTA
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000115840:ENST00000422440:17
Average complexity
IR
Mappability confidence:
NA
Protein Impact

Alternative protein isoforms

No structure available
Features
Disorder rate (Iupred):
  C1=0.000 A=NA C2=0.164
Domain overlap (PFAM):

C1:
PF0015322=Mito_carr=PD(28.1=87.1)
A:
NA
C2:
NO


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:
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

  • Autistic and control brains