Special

HsaINT0158394 @ hg19

Intron Retention

Gene
ENSG00000197694 | SPTAN1
Description
spectrin, alpha, non-erythrocytic 1 (alpha-fodrin) [Source:HGNC Symbol;Acc:11273]
Coordinates
chr9:131377911-131380039:+
Coord C1 exon
chr9:131377911-131378119
Coord A exon
chr9:131378120-131379918
Coord C2 exon
chr9:131379919-131380039
Length
1799 bp
Sequences
Splice sites
5' ss Seq
CAAGTATGT
5' ss Score
7.44
3' ss Seq
GTTTCCCATCTCTCATTCAGGGA
3' ss Score
9.38
Exon sequences
Seq C1 exon
GATCGCCTGAAGGACCTGAACAGCCAGGCAGACAGCCTGATGACCAGCAGTGCCTTCGACACCTCCCAAGTAAAGGACAAGAGGGACACCATCAACGGGCGCTTCCAGAAGATCAAGAGCATGGCGGCCTCCCGGCGAGCCAAGCTGAATGAATCCCATCGCCTGCACCAGTTCTTCCGGGACATGGATGACGAGGAGTCCTGGATCAA
Seq A exon
GTATGTCTTCTCAGCCCTCTAGAAGGCCCCTTACGCCTGTAATAGTGGGCAGCAGGAACCACAGGCTGACTGTTGAGTGGTGAGGCTGGAAACCCTGCTGGACTGGGATCCCAGCTTGGGCACACAGTCGTGGGATGCCTCAGTGTCTTCTGCTTTCCGGGTTTACAGTGATGATAATTGGCGGTGGTGGTGATCCATGCTGGCTACATAGGCCCTGTCTAGACCCTGCCTTTTAGATTCCCGTGAAAGTTAGTGAGTTTGTTTCTGAGCTTCTGGAGAAGATCACTTCTCCAAGGAAGGAGTTGCTTTTTTTCTTATTCTCTATCTGTCCCCGAAAATGTCAGTCTACTGATTCCAGTTGATGTGGCAGGTAAACAAACATTTTTTTTTCTGAGATGGAGTCTCGCTCTGTCACCAGGCTAGAATGCCACCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACTATGTTGGCCAGGCTAGTCTCGAGCTGACCTCACCTGACCTCAAGTGATCCACCCACCTGGGCCTCCCAAAGTGCTGTGATCACAGGCATGAGCCACTGCGCCTGGTCGGAAGGCTTTAAGGAAGTAAGGAATTAAGAGAGAGGATTTTGTTCTTAAAAGACGTTTGTGGCCGGGCGCAGTGGCTCACGCCTGTGATCACAGTACTTTGGGAGGCTGAGGCGGGCAGATCACTTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCCGTCTCTACTAAATACACAAAAATTAGCCAGGTGTGGTAGCAGGCGCCTGTGGTCCCAGCTGCTTGTGAGGCTGAGGCAGGATAATCGCTTGAACCAGGGAGGCGGAGGTTGCAATGAGCCAAGATCGCACCACTGTACTCCAGAGCAAGACTCCGTCTCAAAAAAATAAAAAATAAAAATATAAAAATTAGCTGGGCATGGTGGCACGTGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATGATTTGAACCTGGGAAGTGGAGATTTCAGTGAGCCAAGATCGTGCCACTGCACTCCATCCTAGGCGACAGAGCAAGACTTTGTCTCAAAAAATATATATATTACTTATATAGCTGGGTGTGGTGGCTCACGCCTATAATCCCAACACTTTGGGAGACCGAGGTGGGCAGATCACTTGAATCCAAGAGTTTGAGACCAGCCTGGGCAACATGGTGAAAACTCATCTCTACCAAAAATAGAAAAAATTAGCCAGGCATAGTGGCGCACACCTGTGGTCCCAGCTACTCCGGAGGCTGAGGTGGGAGGATCACTTGAACCGGAGTGGCGGAGGTTGCAGTAAGCAGAGATCATGCCATTGCACTTTAGCCTGGGCAACAGAATGAGACTCTGTCTCAAAAAAAAAAAAAGTGTGTATATATGTATATATATAAATATCTTTGTATATTTACAGACATATATTGATATATTAATACATATTTAGTATACATGATTGATATATATTGATATAATTTGATAGGGCTCCTCAGGGCAGCACTAGTGATGCCTCCCATCCTCCAGTGCATCCCCAACCCTCCAGAATCCGGACACACAGCAGGGCTCATAGATGCATAGATGGACAGAGGTTCTTGGTCCCTACTCATTTGGGAAGTAGAGGCTTTTGTTGTTCAGAAAACTGGCAAGGATTTTCCCAGAAAGATTAGTAGATGTCTGTGAGGTCCACAGTTGACCTGATGTCCCCACTTGAAAGCAGGGAGGTGCAGAGACTGACTGTGCTGTTTCCCATCTCTCATTCAG
Seq C2 exon
GGAGAAGAAGCTGCTGGTGGGCTCAGAGGACTACGGCCGGGACCTAACCGGCGTGCAGAACCTGAGGAAGAAGCACAAGCGGCTGGAAGCAGAACTGGCTGCGCATGAGCCGGCTATTCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000197694-SPTAN1:NM_001130438:41
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.122 A=NA C2=0.070
Domain overlap (PFAM):

C1:
PF0043516=Spectrin=PD(47.6=71.4),PF0043516=Spectrin=PU(16.2=24.3)
A:
NA
C2:
PF0043516=Spectrin=FE(38.1=100)


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:
GATCGCCTGAAGGACCTGAAC
R:
CTGAATAGCCGGCTCATGCG
Band lengths:
330-2129
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains