AutismKB 2.0

Annotation Detail for GRIPAP1


View Evidences View Variants View Annotations
Basic Information Top
Gene Symbol:GRIPAP1 ( DKFZp434P0630,GRASP-1,KIAA1167,MGC126593,MGC126595 )
Gene Full Name: GRIP1 associated protein 1
Band: Xp11.23
Quick LinksEntrez ID:56850; OMIM: 300408; Uniprot ID:GRAP1_HUMAN; ENSEMBL ID: ENSG00000068400; HGNC ID: 18706
Relate to Another Database: SFARIGene; denovo-db
Post Translation Modification Top
Location(AA) Modification
655Phosphoserine.
666Phosphoserine.
669Phosphoserine (By similarity).
690Phosphoserine.
692Phosphoserine.
Location(AA) Modifications Resource
666Phosphoserine (By similarity).Swiss-Prot 53.0
669Phosphoserine (By similarity).Swiss-Prot 53.0
Location(AA) Modification Resource
47Phosphotyrosine(Jak)HMM predict
60Phosphoserine(PKC)HMM predict
84Phosphoserine(CK2)HMM predict
84Phosphoserine(ATM)HMM predict
84Phosphoserine(CK1)HMM predict
93N-linkedHMM predict
182O-linkedHMM predict
247Phosphothreonine(PKC)HMM predict
254N-linkedHMM predict
258N-linkedHMM predict
377Phosphotyrosine(Syk)HMM predict
377SulfotyrosineHMM predict
425Phosphoserine(PKG)HMM predict
535Phosphoserine(CK1)HMM predict
643Phosphoserine(CK2)HMM predict
655Phosphoserine(CDC2)HMM predict
655Phosphoserine(CDK)HMM predict
661Phosphothreonine(PKC)HMM predict
688O-linkedHMM predict
690Phosphoserine(CK1)HMM predict
690O-linkedHMM predict
691O-linkedHMM predict
692Phosphoserine(CDK)HMM predict
692Phosphoserine(CDC2)HMM predict
704PhosphoserineHMM predict
704Phosphoserine(CK1)HMM predict
Validated transcription factor binding site by ChIP-Chip and ChIP-Seq
  • RefSeq ID: NM_020137
  • Location:chrX 48715077-48743618
  • strand:-
No data
No data
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
CTCF G2GSE9613 48716531 48716905 374 0
CTCF G2GSE9613 48717240 48717833 593 0
hScc1 G2GSE9613 48717240 48717833 593 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