Special

HsaINT0145812 @ hg19

Intron Retention

Gene
Description
sodium channel, voltage-gated, type II, alpha subunit [Source:HGNC Symbol;Acc:10588]
Coordinates
chr2:166234107-166237239:+
Coord C1 exon
chr2:166234107-166234160
Coord A exon
chr2:166234161-166237101
Coord C2 exon
chr2:166237102-166237239
Length
2941 bp
Sequences
Splice sites
5' ss Seq
AATGTAAGT
5' ss Score
8.62
3' ss Seq
CAATTCTTCATATTCTTTAGGTA
3' ss Score
8.48
Exon sequences
Seq C1 exon
GCCACGTTTAAGGGATGGATGGATATTATGTATGCAGCTGTTGATTCACGAAAT
Seq A exon
GTAAGTCTAGTTAGAGGGAAATTGTTTAGTTTGATTAAATGTATATTTCTACAATATTGTAATTTAGTGATATTGTCAATAAAATAAAATTATGTGCTTAATTTATAAAACCCATCTATATTATAAGGATAAAATATTTAATCATACTATTTCTTTCAAAATTATCATAGGATGATTTTCTCTAATCACTCTGTATCTTTTAACATATCTTTTCTAGTATTTAGCAAGGCACCTGACACAAAACTTTATTGTATGTATTTTCAAAATGAGACATTTTATTTTTGGCTCTGATAGTCCTGGTCATTTGTGCATTAGAAGTTCTCACAGGCAATATTTTTTATCTGTAATATATTTCCTCCAGCTTTTGATCTTCCTTATAATAGGAAGGATATGACTAAAAACGGGGACAAAAATAAACAATTTAGTGTTTCTCTTGGGAAAGTGAGATTAAGTGGTAGAAGGGAGGGACTTCCCTAATCTACTTTATACATACCAGTACTTTGAATTCTTTTCTATAATTTTCATTAATTTCTCACTATTTAATGAGGAATGAAGTCACATTTTGAAAAAAAAAAAAAAAGAGATTGATTTCTGGTATGCCAGAGCATGATAATAAAGCTCAAAATGCTCTTTCCCTAGCACCAGCAGCTAGCTTTCTGAGTGAAGAATTCCTGAGGTTTTTTTTTTTCTTTTTTCCACTTCATAAAAACAGAGAGGGAGCAAGAAAGCATGAAAAGCCCTGCATTGTATCTCTATAAGTGCTATCAGGAATTCCAGTTATGAGATTTTTCTGAATAGTAATAATAATTTATTGATTATCACTATTCACTGTGCCAAGGACTTTCTCACATTATCCCATTTAATCCTAAATGACAACCTTATTGTATAGGTGATACTAGCTCTATTTTACTACTGAAGCAAAGAGGCTTAATGCGTTAAATGGGAAAACAAGTTTTTGAACCCTGACCACAAATAATGGCTCATACCCACTTTCCACAGTGGTTCTTACCTTTTTGATTAATTAATTCAATGCTCTCTCCACCTTCCTTATCAATAGCTTATATGCCATGAAACATTTTCAGTTTCTTCTTTAATAACTTAGCAGACCTTTTCCGCTGCAAAACTCCTGGAATTTCCAGCACATTACAAAAGATGAAAGCCAATTGAGCACTACATTTATGAAAAGTTGCTGGATCTTGAACTTTAATTAGTAAATTGCATCAGATAAATGCAAATTTAAACCAAAATAAAACATTATCTACACACCTACCAGATTGGCAATACCAAAAAGTCTGACAATACCAAGTTTTACCAAGGATAAACAGCAATAAGAACACTCGTACAATGCTGATAGGAAAAAAAATAGTTAAATAATCCTTTAAAAACAGTTGGGTATGATCACATTATTTGAGAAAGTTAAAGATATTTTTTAATACTGCAATTCTACTTTGAACAACGTATCCTAAAGAAACTTATGCACATGTTTAGGATAATCTATGTACAAAAATGAATATAACTTTTTTTTGCACTTGCAAAAAACTGGGAGCAACTCAAAAACAGTAGAAATAGGCAAATAATTGAATACTATATAGTGATGAAAATGAATGAATACCGCCATATACAACCACATGGATGAGCCTTAAAAATACAACATTGAGTTAAAGAAACTAGACACATACTATAATTCTACTTATATAAAGTTCGAAATTGACAAAACTAAGCTTATTGTTCAAAACTGCATACTGAGGTGTTAACTTGAAAGAAAAAGCAGGGACATCATTACCATAAAAGTCAGGATAATGATTACCTCCAGCAGGGATGATGGAGTTTATGTTTGAGAAGGGTACACCAAGGGTTTCTGAAGTTGTAGCAATGTCCTGGGTTATGGATTTCACTTATAAAACATATTATATTTTGCATTTATGTATTATGCACTTTCCTGTATGTATATTGTCTTTTAAAAATTTTAAAAATATAATTTTACATCACTGTTAACTAAACTCACATACACAAATAAAATCTCATCGAAGAATAGCAGTTTTACAATATTCCTGATATTTTCCATTTTGCTGTATTTCCTTAGAAACAAAATTATGCTGGTCATAATCCTCTAAATTGATTTCATAACACAGTGGGTTATAACTTGCATCTATTATCATCATCAGGGATTGGTTAACTGAGTTGGTTAGAACAATGTCCTATTAGACCTGTGAAAGCTTACAGCTAAGGCGCAAACCTACTATCACACAGTTTTCTAAACAAAAGTGGATTAGACAAGAGATAGTATCATTGTTACAGAAACAGTCCCTACTGAATAGGATAAAGCAATAGATTCATTTTCAGAAAGGAAAGATCAACCTATATACCTACATGCAGACCTACTACAATGATTCTTGCCTATCTAAAGAAATGTATTATACCAAACCCTTACACTTAGCAATTACTACTGGCCGCCACTGTTCTAAGCATATTTATATGTTAATATAGTTAATCTTCACAACCACACTATGAGGTTTAAGTTTGATTATTTTCATCTCACAGATGAGAAAACTGAGTCAGAGAAAGTAAATCTTAAAAGTTTTGACATAGAATAATGTGACGCTGACATCTCTTTTGTAAGAAGAGGAAATCTTTAATTTGCATGCTGTGTTGGGAACTTTGCTTAGAAAGGAAAGTGCATTCATAATCTGGGCATTTGTTGGGTGAAATTGTCTATAATCATTCAGACTTCTATATGGTTATTTCATTTTCCCAGGTAATGAATAGTCTTGCAGAACTCTTCAATAAGCATGTGAGATTTGAAGGTTCATAAAATCTGTTTAGTGTTTGGTTTATTTTCATTCCAGAGATTAAAACATGCTTAGATAATTAAAAACTCACTGATGTACTTTTTGTGAAACAAGTACTAGATATAATGGTTACAATTCTTCATATTCTTTAG
Seq C2 exon
GTAGAATTACAACCCAAGTATGAAGACAACCTGTACATGTATCTTTATTTTGTCATCTTTATTATTTTTGGTTCATTCTTTACCTTGAATCTTTTCATTGGTGTCATCATAGATAACTTCAACCAACAGAAAAAGAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000136531-SCN2A:NM_001040142:23
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:
PF0052026=Ion_trans=FE(7.4=100)
A:
NA
C2:
PF0052026=Ion_trans=PD(15.3=76.1)


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:
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
  • Pre-implantation embryo development