Special

HsaINT1041879 @ hg38

Intron Retention

Gene
ENSG00000181240 | SLC25A41
Description
solute carrier family 25 member 41 [Source:HGNC Symbol;Acc:HGNC:28533]
Coordinates
chr19:6432049-6433779:-
Coord C1 exon
chr19:6433487-6433779
Coord A exon
chr19:6432205-6433486
Coord C2 exon
chr19:6432049-6432204
Length
1282 bp
Sequences
Splice sites
5' ss Seq
CAGGTGAGT
5' ss Score
10.67
3' ss Seq
GGGCCGGGTCTGCCCTGCAGGTA
3' ss Score
7.83
Exon sequences
Seq C1 exon
AATCCTCCCACTAGACACTCCCGCATGGTAGCTGGAGCAGCAAACAACTGCTTAGGGATTTGAAGCCAGGTGTCCTAACTTCCTCCATGGGCGCTCAGCCTGGGGAACCTCAGAACACTTGCTCTAGGATCCAGACACTGTTTAGGAGGGTCAAGACCTTACTCATCAAAGCCCCGCCTCCCCCCCAACCTCCGCCTCCACCCCCATCCTGGAACCCTGGCTGTACACACGTGTATGGGTACGCGTTTGGCCACATGCATGACAACAACCTTGAACATCTCCCGTCACAGCAG
Seq A exon
GTGAGTTTAGGAAACACCAGTGTCCCGGCACCTCTGGTCAGGACTACAGGGAGAGGCCAGGCTACCCACGCCCTCTACAGGCCCACTCCCCTGCTAGCGGACCTAGAATTCCACCTTGAAGCAGGGTGGGGCAGGGAGGCAGGGCGCGATGGCTCCACACATGTAATCCCAGCACTTTGGGAGGTTGAGGTGGATGGGTCACTTGAGGACAGGAGTTCAAGACCAACCTGGCCAACATGCCGAAACCCTATCTCTACTAAAATTACAAAACTTAGCCAGGCATGGTGGTTGGCGCCTGTAGTACCAGCTACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAACTCAGGAGGTAGAGGTTGCAGTGAGCCCAGATCTCATCACTGCACTCAAGCCAGAGCAACACAGCGAGATTCTGTCTCAAAAAATAAGAATAAATTAAGAGTCTAGATATAGTCCTAATTACATTTGTATTCCTCCTTGGATCCTCCATGAGTAACTTAGAGAGTCTATATTACATTGGCTGGGTGTGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGTGGATCACCTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACCCTGCCTCTATTAAAATAATACAAAAATTTGCTCGGCACGTTGGCACTGTAATCCCAGCTACTGGGGAGGCTGAGGCAAGAGAATCACTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCCGAGATCACACCATTGTCCCTACTTGGGAAGCTGAGACACGAGAATCGCTTGAACCAGGGGGACAGCGGTTGCAGTGAGCCAAGATCGCACCACTGTACTCCAGCTTGGGCGATAGAGTGAGACTCTGTCTAAAAAAAAACAAAAACAAAACAAAAAAAAACCAGGGGGGAGGGTTGAATCACTTGAGGTCAGGAGTTAGAGACCAGCCTGGCCAACATAGTGAAACCCATCTCTACTAAAAAAAAAAAAAAAAAAAAAAAAAAAAATTAGGTGTTGTGGTGCATGCCTATAATCCCAGCTACTCAGGAGGCTGCGGCAGGAACTGCTTGAACCTGGGAGGTGGAGGTTGCAACGAGCTGAGATTGTGCCACTGCACTCTAACCTGGGCAGCAGAGCAAGACTCCGTCTCGAAAAAAAAAAATGCAGACTTGGGGGAACAGGGTGGGTCTTTCACCAGGTGGGTGCCCTAGATGTGTGTCTGGGGAAGGTGCCCCAACCTGGCTGAGGATGAGGGAGGGCCGGGTCTGCCCTGCAG
Seq C2 exon
GTACTGGACACAGGAGAGCAGCTGATGGTCCCCGTGGAAGTCCTGGAAGTGGATAACAAGGAGGCCTTGTGGAAGTTTCTACTCTCAGGAGCTATGGCCGGGGCGGTGTCTCGCACGGGCACGGCACCTCTGGACAGAGCCAAGGTGTACATGCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000181240:ENST00000597558:1
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion (1st CDS intron)

No structure available
Features
Disorder rate (Iupred):
  C1=0.548 A=NA C2=0.064
Domain overlap (PFAM):

C1:
NO
A:
NA
C2:
PF0015322=Mito_carr=PU(35.5=63.5)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GCTTAGGGATTTGAAGCCAGGT
R:
CGGCCATAGCTCCTGAGAGTA
Band lengths:
344-1626
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains