AutismKB 2.0

Annotation Detail for SSPN


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Basic Information Top
Gene Symbol:SSPN ( DAGA5,KRAG,NSPN,SPN1,SPN2,nanospan )
Gene Full Name: sarcospan (Kras oncogene-associated gene)
Band: 12p11.2
Quick LinksEntrez ID:8082; OMIM: 601599; Uniprot ID:SSPN_HUMAN; ENSEMBL ID: ENSG00000123096; HGNC ID: 11322
Relate to Another Database: SFARIGene; denovo-db
Post Translation Modification Top
Validated transcription factor binding site by ChIP-Chip and ChIP-Seq
  • RefSeq ID: NM_005086
  • Location:chr12 26239788-26277133
  • strand:+
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
CTCF G2GSE9613 26239530 26239979 449 34
FoxA1 MCF7MACSdata 26230021 26230146 125 9705
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
CBP T30-glioblastomaGSE21026 26283213 26284474 1261 6710
FOXA1 DLD1GSE12801 26290717 26291077 360 13764
FOXA1 MCF7GSE15244 26290785 26291147 362 13833
P300 T30-glioblastomaGSE21026 26282906 26284642 1736 6641
RARA MCF7GSE15244 26283843 26284445 602 7011
RARA MCF7GSE15244 26290785 26291501 716 14010
RARG MCF7GSE15244 26283255 26284374 1119 6681
RARG MCF7GSE15244 26290754 26291464 710 13976
TFAP2C MCF7GSE21234 26290667 26291211 544 13806
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
CTCF G2GSE9613 26271022 26271163 141 0
FOXA1 MCF7GSE15244 26270235 26270548 313 0
RNAII Tamoxifen-MCF7GSE14664 26253505 26253544 39 0
TAF HelaGSE8489 26264645 26264822 177 0
hScc1 BcellGSE12603 26239683 26239979 296 0
hScc1 BcellGSE12603 26270992 26271256 264 0
Validated miRNA targets Top
Cis-Nats regulation Top
Cluster ID Plue Type Plus Gene Name Plus Chromosome Plus Start Plus End Overlap Length Minus Type Minus Gene Name Minus Chromosome Minus Star Minus End Type
5803 mRNA SSPN chr12 26239788 26277134 364 EST chr12 26275018 26363920Sense/Antisense (SA) pairs

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