Special

HsaINT0152830 @ hg38

Intron Retention

Gene
ENSG00000169507 | SLC38A11
Description
solute carrier family 38 member 11 [Source:HGNC Symbol;Acc:HGNC:26836]
Coordinates
chr2:164911636-164915273:-
Coord C1 exon
chr2:164915112-164915273
Coord A exon
chr2:164911749-164915111
Coord C2 exon
chr2:164911636-164911748
Length
3363 bp
Sequences
Splice sites
5' ss Seq
AAGGTAAAA
5' ss Score
8.38
3' ss Seq
TATTTTATATTACTATCTAGGGG
3' ss Score
7.09
Exon sequences
Seq C1 exon
CATTTATTTGCCACCATAACTCCTTCTTAGTTTACAGTTCTCTAGAAGAACCCACAGTAGCTAAGTGGTCCCGCCTTATCCATATGTCCATCGTGATTTCTGTATTTATCTGTATATTCTTTGCTACATGTGGATACTTGACATTTACTGGCTTCACCCAAG
Seq A exon
GTAAAATGAGAGATTCAGTTATAGTGTTCATGTGCATTGGTACAGGTATACCGAATGTTCTACTCATTATTGTTACAGGTATGCCCAGTGTTCTATTTCAAAGATTACTCTCTTCCACCCATTCTCTCTACCCTCCTGCCCCCCTGCTGTCTGTTTCCTAGTTTTTACCTTTTTAAACTGCTCAATTTAGTTCTGTAGCCCATACTCTCTCCTTCCACACACTGTCACTTCCTAGCACATGATTTTTGGCTTTCCTCCACTGCAGCTTCATTTTCAAAGGTACCAGTGGCCTCCCAATCTTCAGAGCAAATAGCTTCGATTTGGATTCTCCCGAATCTCTCTGAATCACTTAACAATACTGAACTTCCTTTCTTTGCTCAAATTTTCCTCCCTTAGAGGAAAGAGTATTATTATATTATCATTGTTATTCTTTCTCTCTGTTAATTTTTTTTCTGTTTTCTTTTTCTTTACCCTCTCTAATCCCCCACTCCACTCCATCCCACACCACCCAGATAACGGGCTCAAGCATATTGTTTTCTCTTCTCTCAAAAAAATTTCCCGGTACTTTCATTGTTTTAATTCTAACCCAGACCTTTCTTTTTGTCTCCAACCTGCTGCCTGTAGGACGTTTCTACTCAGTTGTTCTATATTTGTCTTAATCACAAAACATCATGTTTCCCTTAAAACCAGACCTTTTCTTCCTCCCTCCAAAGATATTTCTCTCTTTTTTTGCATTCACCCAGGCCCAGCAACTGAGCAGTCCTCTCTTCTACTTCCCTTGACCCTTACATTCAATCATCAGTGTAGTGTAGTAGTCAGGGCAGTCCAGCAGTAGGCTGTGATTTACATATTTCACAGCTCTTGCAGGTCTATTATCTCATTGACCTTCAGACAACCCTTTGAAGGGAAGTGGAATAACTAGTTTTACCCCCTGATTAAAACACAAAGAGGTGAAGTAACTTGCTCATGCTGGCTGATGACAAACCAGAAAACAAGTCTTCTGACTCTTAAGTTCAGTTTTCTTTCCATCCTCTTTCTGCCTGCCCTGTTTTGGTCAACCATGACCCTCTGAAAGTTGTCCCTTTGCCTCTAGCTCCCATTAGCTTAGTTTTCTGAAAACCTGGGTGCTCTTGGGAGGATGGCTGCCTTATTCTGAACAGAGGTTACAGATCACTATGACTTTAGGCAAATATTTCTCAAGAAATGAAGAAAGATGGCTTCAAAAAATAATGATTAACAAAATTCAAATGCAGTCAAAAATATAATACATGCCTGTGCCACTAGAGTGCAGTAACAAAGTGACCTTGAAACTTCTGATAAGAATTGTGTTCCAAAGCATTTCTATGTATCACTATTGCTACATAGTTTGCCAATGCAAATGGCCTATGGGCTCTGGTCTGTACAGGACCTTGGTTTTTAAATGCCTTTTCTGTAAGACATAACCTTTTTTGTTAGTTACATCTTCCTGGAGTTTTTATCAGTGGTAATTGCTCAGATATAATTAAATCTTTATAAAACAAAGCTGACAGGTTTTTAATGCCGTTTTCCCCCTAGCTGTAATTCTTTAAAATACAACTTAGATTCAGGCTGCAATAAGCTGACATTGTTTCTCCAGGCCACCTCTCCTTAGGTAAATCTAGTCTAATTTGTGCATACTGCATTCTTCTTTTCTAACCTCTTTCAGTAGATAAATTTCAGCTTGAGAGGCGGTGGGAACTCTAGATTCTCCTCGACATTTCTAGTGACTTTCGAAAAGACAATAGGGCTCATTTTTTTAGTGGAGGTTAGTGAACGGGGAACTTCAGTCCTTTTTTCTTAGAGTGCTGGAATCTTTTCAGTCAACCTTGAAGCAGGTTTCTGCCACCTTACTTTGTGTTTTAATCCCCTCCTGCCCAAAAGGGATGTTCTAAAGTAATGTAGATTTGTTCTAGTTGATGGGGGGAGGGGTGAGAGCCACTTAAAGTAAATCTTGGGAAGAGGCAAATTATTTAGGATATTCAGCTTTGTAATGAAAAAAACAGTACAGAGGTATTATAGCTTTTCTTCTTTTTAAATGGTGTAGTATTGAGTATTGATCTTAAAAAAATTTAATTTTCAATTAAGTTTAATTTTAAAAAGGTTACCACAATTTTAACATTTAAGCACGTTATATACAGAAAATCAGCAAGCCCAAGTACTCTGTTTCGGCATTAGTCATTGTTATATTTTTATTTTTTTTATTTCTTCCATGGACTACTGTACAGTTGTAGGTAATTGTTTTTTGATGACATGACATCTGTGCCCTAGTTAGATCCCTGTATTTCTTCATAGACAGTTGAGAAATATAGTCTCTAAATAAGAATTGTTTCAAGGTATATTTAGTCCATCATCTAGTCTGGAACTTATTAAATTTAATGTTCTTTCTGGGACATAGCCATATTTTCACAGTTTTGAATCAGTGCATTTACACTTGGGCTCATGAGGTGCCATGAAAGGTAACATATGTTTGGAATTTCTCGCTGTGGCCCCAAGGTTGGGATGAAACCCTATAGCATGATACACAGGAAATTCAGCTCCCCAGATGTACTGGTTTACTCTTCCTTTCAGGATTGTTCTTGATCTAAGAATAGCATTTCAAAAGGAAATTTGTTTATTTTTAACAGACATTTTTAAAAAATAATGAAGTCACTTACTCACCAGAAACAAAGACCAGAAACCAGTTTACAAAGCCAGTGCTGAAGAATTTAGGGAGTTGATTCTGATGTAAGAAGACAATGGATAAAGTATTTTTCAGAAGTCAGTACAAATTGGCAGCAAATCTACCAAAAACAAATAATAAGAGAAAAACTATCAGTGATGGATTTATCTTCACATGTAGCATGTACTGGTTTAAATCAGTGAATAACTACATAGTTATTGAATTCAAAAACTTTTATTTAGACCTGGTCATCTATTCTCTTAATTAAATGAAATGAAGTTTATGGAGATTCACTTATAAGTCATGTGTTGCTTAATGACAGGGAAACATTCTGAGAAATGCATTGTTAGGTGATTTCCTCATTGTGCAAACATCACAGAGTATACGTACACAAATCTAGATGGTAGCACCTATTACACACCTAGGCTATATGCTATAGCTTATTGCTCCTAGGCTATAAACCTCTACAGCATGTTTCTGTACTGAATTCTGTAGGCAACTGTAGCAGAATGGAAAGTATTTATGTATCTAAACATAGAAAAATATATAGTAAAAATACAGCATTGTAATCATATATGTGGGCCATTAGGTGATGCATAACTGTAATATCTAATATTTAATTTATTAGATAGTTATCTCAAACATTTAGTATCTAGTAAATAAACTTATTTTATATTACTATCTAG
Seq C2 exon
GGGACTTATTTGAAAATTACTGCAGAAATGATGACCTGGTAACATTTGGAAGATTTTGTTATGGTGTCACTGTCATTTTGACATACCCTATGGAATGCTTTGTGACAAGAGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000169507:ENST00000303735:7
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:
PF0149013=Aa_trans=FE(15.8=100)
A:
NA
C2:
PF0149013=Aa_trans=FE(10.8=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
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

  • Genotype-Tissue Expression Project (GTEx)
  • Autistic and control brains