AutismKB 2.0

Annotation Detail for SEZ6L


View Evidences View Variants View Annotations
Basic Information Top
Gene Symbol:SEZ6L ( - )
Gene Full Name: seizure related 6 homolog (mouse)-like
Band: 22q12.1
Quick LinksEntrez ID:23544; OMIM: 607021; Uniprot ID:SE6L1_HUMAN; ENSEMBL ID: ENSG00000100095; HGNC ID: 10763
Relate to Another Database: SFARIGene; denovo-db
Post Translation Modification Top
Location(AA) Modification
311N-linked (GlcNAc...) (Potential).
328N-linked (GlcNAc...) (Potential).
350N-linked (GlcNAc...) (Potential).
435N-linked (GlcNAc...) (Potential).
458N-linked (GlcNAc...) (Potential).
474N-linked (GlcNAc...) (Potential).
514N-linked (GlcNAc...) (Potential).
576N-linked (GlcNAc...) (Potential).
618N-linked (GlcNAc...) (Potential).
674N-linked (GlcNAc...) (Potential).
742N-linked (GlcNAc...) (Potential).
Location(AA) Modifications Resource
No data
Validated transcription factor binding site by ChIP-Chip and ChIP-Seq
  • RefSeq ID: NM_021115
  • Location:chr22 24895479-25106433
  • strand:+
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
H3K27me3 colorectalcancer 24892490 24892844 354 2813
NRSF mAbJurkat 24892106 24892844 738 3005
STAT1 HeLaGSE12782 24887504 24888734 1230 7361
STAT1 HeLaGSE12783 24887728 24888649 921 7291
STAT1 IFNSISSRdata 24887758 24888374 616 7414
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
CTCF CD4GSE12889 25124731 25124888 157 18376
CTCF CD4SISSRdata 25124731 25124888 157 18376
CTCF G2GSE9613 25124662 25124917 255 18356
hScc1 BcellGSE12603 25124662 25125164 502 18480
hScc1 CdLSGSE12603 25124662 25125096 434 18446
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
CBP T30-glioblastomaGSE21026 25048182 25049203 1021 0
CTCF CD4GSE12889 25057028 25057258 230 0
CTCF CD4GSE12889 25086360 25086688 328 0
CTCF CD4GSE12889 25093713 25093994 281 0
CTCF CD4SISSRdata 25057028 25057258 230 0
CTCF CD4SISSRdata 25086360 25086688 328 0
CTCF CD4SISSRdata 25093713 25093994 281 0
CTCF JurkatGSE12889 25056985 25057250 265 0
CTCF G2GSE9613 24895612 24895793 181 0
CTCF G2GSE9613 24898338 24898913 575 0
CTCF G2GSE9613 25044891 25045330 439 0
CTCF G2GSE9613 25056824 25057257 433 0
CTCF G2GSE9613 25086223 25086714 491 0
CTCF G2GSE9613 25090580 25090825 245 0
FOXA1 MCF7GSE15244 24900193 24900671 478 0
Fos K562GSE19551 24965457 24965864 407 0
Fos K562GSE19551 25082661 25082934 273 0
H3K27me3 colorectalcancer 24896208 24897848 1640 0
NRSF JurkatGSE13047 24896175 24897160 985 0
NRSF JurkatGSE13047 24985120 24986113 993 0
NRSF JurkatGSE13047 25039210 25039702 492 0
NRSF mAbJurkat 24896321 24898913 2592 0
NRSF mAbJurkat 24980661 24982417 1756 0
NRSF mAbJurkat 24983197 24986072 2875 0
NRSF mAbJurkat 24987495 24989148 1653 0
NRSF mAbJurkat 24989515 24991405 1890 0
NRSF mAbJurkat 24995333 24996477 1144 0
NRSF mAbJurkat 25039106 25041115 2009 0
NRSF-mono JurkatQuESTdata 24896585 24897159 574 0
NRSF-mono JurkatQuESTdata 24985215 24986106 891 0
NRSF-mono JurkatQuESTdata 25039293 25039637 344 0
NRSF-poly JurkatQuESTdata 24896340 24897325 985 0
NRSF-poly JurkatQuESTdata 24985231 24985931 700 0
NRSF-poly JurkatQuESTdata 25039175 25039729 554 0
P300 T30-glioblastomaGSE21026 25034709 25035424 715 0
P300 T30-glioblastomaGSE21026 25046895 25049060 2165 0
P300 T30-glioblastomaGSE21026 25082646 25083068 422 0
RARA MCF7GSE15244 25079793 25080082 289 0
TFAP2C MCF7GSE21234 25048477 25048993 516 0
hScc1 BcellGSE12603 25018571 25018906 335 0
hScc1 BcellGSE12603 25052169 25053154 985 0
hScc1 BcellGSE12603 25056715 25057492 777 0
hScc1 BcellGSE12603 25103503 25103724 221 0
hScc1 CdLSGSE12603 24895612 24895949 337 0
hScc1 CdLSGSE12603 25056752 25057492 740 0
hScc1 CdLSGSE12603 25086186 25086753 567 0
hScc1 CdLSGSE12603 25090544 25090881 337 0
hScc1 G2GSE9613 25044855 25045371 516 0
hScc1 G2GSE9613 25056824 25057257 433 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


Copyright © 2017, Center for Bioinformatics , Peking University | All Rights Reserved