AutismKB 2.0

Annotation Detail for MID1


View Evidences View Variants View Annotations
Basic Information Top
Gene Symbol:MID1 ( BBBG1,FLJ57031,FLJ58683,FLJ76288,FXY,GBBB1,MIDIN,OGS1,OS,OSX,RNF59,TRIM18,XPRF,ZNFXY )
Gene Full Name: midline 1 (Opitz/BBB syndrome)
Band: Xp22
Quick LinksEntrez ID:4281; OMIM: 300552; Uniprot ID:TRI18_HUMAN; ENSEMBL ID: ENSG00000101871; HGNC ID: 7095
Relate to Another Database: SFARIGene; denovo-db
Post Translation Modification Top
Location(AA) Modification
90Phosphoserine.
92Phosphoserine.
96Phosphoserine.
98Phosphoserine.
Location(AA) Modifications Resource
92Phosphoserine.Swiss-Prot 53.0
92PhosphoserinePhospho.ELM 6.0
98Phosphoserine.Swiss-Prot 53.0
98PhosphoserinePhospho.ELM 6.0
Location(AA) Modification Resource
45N-linkedHMM predict
76N-linkedHMM predict
81N-linkedHMM predict
90Phosphoserine(IKK)HMM predict
92Phosphoserine(IKK)HMM predict
92O-linkedHMM predict
96Phosphoserine(CDK)HMM predict
96Phosphoserine(IKK)HMM predict
96Phosphoserine(CDC2)HMM predict
96Phosphoserine(MAPK)HMM predict
100Phosphothreonine(PKC)HMM predict
311Phosphoserine(PKB)HMM predict
311Phosphoserine(CK1)HMM predict
311Phosphoserine(IKK)HMM predict
311Phosphoserine(CAMK2)HMM predict
314Phosphoserine(ATM)HMM predict
319Phosphoserine(CK1)HMM predict
334N-linkedHMM predict
356N-linkedHMM predict
410Phosphoserine(CK1)HMM predict
459Phosphotyrosine(INSR)HMM predict
503N-linkedHMM predict
513Phosphoserine(CK1)HMM predict
518Phosphothreonine(CDC2)HMM predict
518Phosphothreonine(MAPK)HMM predict
667ProlineHMM predict
Validated transcription factor binding site by ChIP-Chip and ChIP-Seq
  • RefSeq ID: NM_000381
  • Location:chrX 10376165-10548458
  • strand:-
No data
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
Nanog hESGSE18292 10369652 10369939 287 6370
TFAP2C MCF7GSE21234 10372122 10372571 449 3819
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
CTCF G2GSE9613 10525977 10526394 417 0
ER Fulvestrant-MCF7GSE14664 10382025 10382060 35 0
ER Fulvestrant-MCF7GSE14664 10437158 10437191 33 0
ER Fulvestrant-MCF7GSE14664 10514637 10514672 35 0
FOXA1 MCF7GSE15244 10397885 10398439 554 0
Fos K562GSE19551 10510369 10510894 525 0
H3K4me3 colorectalcancer 10547878 10548247 369 0
Nanog hESGSE18292 10436749 10437895 1146 0
Oct1 H2O2-HelaGSE14283 10397832 10397871 39 0
Oct1 HelaGSE14283 10382027 10382060 33 0
Oct1 HelaGSE14283 10397833 10397867 34 0
Oct1 HelaGSE14283 10420144 10420205 61 0
Oct1 HelaGSE14283 10437157 10437204 47 0
Oct1 HelaGSE14283 10489204 10489246 42 0
Oct1 HelaGSE14283 10514636 10514670 34 0
Oct4 hESGSE17917 10526058 10526243 185 0
RARA MCF7GSE15244 10494376 10494827 451 0
STAT1 HeLaGSE12783 10474446 10475305 859 0
Sox2 hESGSE18292 10437065 10437318 253 0
Sox2 hESGSE18292 10539307 10539906 599 0
p130 SenescentGSE19898 10528489 10528752 263 0
Validated miRNA targets Top
Micro RNA Name Stem Loop Name The chromosome that miRNA located Publication
hsa-miR-135b hsa-mir-135b 1 19795981
hsa-miR-135b* hsa-mir-135b 1 19795981
hsa-miR-224 hsa-mir-224 X 19795981
hsa-miR-31 hsa-mir-31 9 19795981
hsa-miR-31* hsa-mir-31 9 19795981
No data
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