Special

HsaINT0158337 @ hg19

Intron Retention

Gene
Description
spectrin, alpha, erythrocytic 1 (elliptocytosis 2) [Source:HGNC Symbol;Acc:11272]
Coordinates
chr1:158606431-158608031:-
Coord C1 exon
chr1:158607823-158608031
Coord A exon
chr1:158606552-158607822
Coord C2 exon
chr1:158606431-158606551
Length
1271 bp
Sequences
Splice sites
5' ss Seq
AGAGTATGT
5' ss Score
5.66
3' ss Seq
GTTTTCTTCCTTGATTTTAGGGA
3' ss Score
10.09
Exon sequences
Seq C1 exon
GATGCACTCAAGGACCTGAATACATTGGCTGAAGATTTGCTCTCCAGCGGGACTTTCAACGTTGATCAGATTGTGAAGAAAAAAGATAATGTCAACAAGCGTTTCCTGAATGTCCAAGAATTGGCAGCTGCACACCACGAAAAATTGAAAGAGGCCTATGCCTTGTTCCAGTTCTTCCAGGATCTAGATGATGAGGAATCCTGGATAGA
Seq A exon
GTATGTGCCACCAGCTCAAAAATGTGTGGATAATACAAGCGAGTAGATAATCCACCAAACTTGTTCCAATTTATGCTGAAATGAAATTTGTACTTGTTTCTTGAAGATAGCACTACTTCATGTTTGCCTCAGCTTAAGGTTAACATTGGTTTTATTTTTCCCAAATTCCCTTACTGGATGCAAGCCAGAGAAAGACAGGTGTGGAGGAAGTGAAGAGCAGTTAACATACATGACAGGAACAAAACTAAGAAGCCATCTGCATTTGCTCTGTAGTTCATTGAATAATATGCAATACTCACAGAGACACCTGGACATTTACACAGCTGATCAGAACCTTGTCATTCTATATCCAGTATATCTTATATGACACTGAATTGGACACTCAATAGAGAATATTACAAAGTATCTACCAAGGTTTCATTACTCATTCCATTTTTGGTTACACAGCTGGTCAGAACCTTGTCATTCTATATCCAGTATATCTTATATGACACTGAATTGGACACTCAATAGAGAATATTACAAAGTATCTACCAAGGTTTCATTACTCATTCCATTTTTGTTGTAAAATATGATTTGGAAAATCTTAGCACATTACACTATTTTGCCTACTTCCCATTTAACCTGCCTCATCACGCTTCTCTTCTACAAAGCTGCTTGATTATTATGAGTAATCAATAAATTAGAGGGAAGCACCATGCACAGGGCAACAAATAACATGTTTTAAAAACCTTTTTGGATAAGACCATAAGATAGAATAATCTTGTCCATGTAGTCTTCGACTGTACTTCGTGGTGATGCTCAAACCTTTTGCACTTGGAAGCATCCCAACTGCCATGACTCCTATGAAATCAGCTCTTTATACCCATTCTAGCTGAATTTATTATTGACATTAATAAATGAAAATAACAAAACCTGTGGAGGTCATATATAATTTTCACATTTTTTTGAAATAGGAAACATTAGTGTGTATTCTTGAGCAAAAAAGAGAAGATATACAAGTGGAGAAGCAAAGGGACTAATGGAAAGGCTGTTACAGTTGTGACTATGGTGGAGATCAGTATGTTACTTTAATTTGTATTGGCTCAGTCAGAAGTTTTGCTGCAAGCCTCTTCCACTAATTATATTTTTGGTCATTGGCACCAGGGTATTACAGAATTTACAACCACCTCCCTCACCACCAGCCACACACATAGTCATAGAAAGCTATTGCTGTAGGATGACATTAGATGTCTAGACTCCAAACTTTCTGTTTTCTTCCTTGATTTTAG
Seq C2 exon
GGAGAAGTTGATACGAGTGAGCTCCCAGGACTATGGGAGAGATCTTCAGGGGGTTCAGAACTTGCTGAAGAAGCACAAACGCCTAGAGGGGGAGCTGGTGGCCCATGAGCCTGCCATCCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000163554-SPTA1:NM_003126:36
Average complexity
IR-S
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:
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
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
TGCACTCAAGGACCTGAATACA
R:
CTGGATGGCAGGCTCATGG
Band lengths:
328-1599
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