AutismKB 2.0

Annotation Detail for SCN4B


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Basic Information Top
Gene Symbol:SCN4B ( - )
Gene Full Name: sodium channel, voltage-gated, type IV, beta
Band: 11q23.3
Quick LinksEntrez ID:6330; OMIM: 608256; Uniprot ID:SCN4B_HUMAN; ENSEMBL ID: ENSG00000177098; HGNC ID: 10592
Relate to Another Database: SFARIGene; denovo-db
Post Translation Modification Top
Location(AA) Modification
45N-linked (GlcNAc...) (Potential).
71N-linked (GlcNAc...) (Potential).
113N-linked (GlcNAc...) (Potential).
Location(AA) Modifications Resource
45N-linked (GlcNAc...) (Potential).Swiss-Prot 53.0
71N-linked (GlcNAc...) (Potential).Swiss-Prot 53.0
113N-linked (GlcNAc...) (Potential).Swiss-Prot 53.0
Location(AA) Modification Resource
45N-linkedHMM predict
53S-palmitoylHMM predict
Validated transcription factor binding site by ChIP-Chip and ChIP-Seq
  • RefSeq ID: NM_174934
  • Location:chr11 117509303-117528744
  • strand:-
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
ER E2-MCF7GSE14664 117530248 117530337 89 1548
p63 keratinocytesGSE17611 117528616 117529746 1130 437
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
Pol2 GM12878GSE19551 117502277 117502877 600 6727
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
CTCF CD4GSE12889 117521212 117521587 375 0
CTCF CD4SISSRdata 117521212 117521587 375 0
FOXA1 MCF7GSE15244 117523629 117523933 304 0
H3K27me3 colorectalcancer 117519744 117520842 1098 0
NRSF pAbJurkat 117513664 117513935 271 0
NRSF pAbJurkat 117521749 117522280 531 0
RARA MCF7GSE15244 117518573 117518944 371 0
Rb QuiescentGSE19898 117521299 117521537 238 0
hScc1 BcellGSE12603 117520983 117522219 1236 0
hScc1 CdLSGSE12603 117520983 117522090 1107 0
hScc1 G2GSE9613 117520911 117521934 1023 0
Validated miRNA targets Top
Cis-Nats regulation Top

Simple Query:


  (e.g. CHD8)

Syndromic Genes

Non-syndromic Genes

AutismKB Statistics

  • Studies: 1,036
  • Genes: 1,379
  • CNVs/SVs: 5,420
  • SNVs/Indels: 11,669
  • de novo Mutations: 5,669
  • Mosaics: 789
  • Linkage Regions: 172
  • Paper Collected: 6/30/2018
  • Last Update: 8/26/2018