Annotation Detail for PHOSPHO2

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Basic Information Top

Gene Symbol:	PHOSPHO2 ( MGC111048,MGC22679 )
Gene Full Name:	phosphatase, orphan 2
Band:	2q31.1
Quick Links	Entrez ID:493911; OMIM: NA; Uniprot ID:PHOP2_HUMAN; ENSEMBL ID: ENSG00000144362; HGNC ID: 28316
Relate to Another Database:	SFARIGene; denovo-db

Pathways, Diseases and Drugs

TF binding site

Post Translation Modification

PTM Sites from Uniprot:0 results
Experimental PTM Sites from dbPTM:0 results
Predicted PTM Sites by profile HMM from dbPTM:5 results

No data

Location(AA)	Modification	Resource
53	Methyllysine	HMM predict
58	Methyllysine	HMM predict
170	N-linked	HMM predict
171	Phosphotyrosine(Abl)	HMM predict
220	Phosphotyrosine(SRC)	HMM predict

Validated transcription factor binding site by ChIP-Chip and ChIP-Seq

RefSeq ID: NM_001008489
Location:chr2 170259220-170266461
strand:+

Upstream the gene:10 results
Downstream the gene:0 results
Inside the gene:5 results

Transcrip Factors	Experimental Cell	Database	TF Binding Start	TF Binding End	TF Binding Length	The Distance to Gene
Nanog	ES	GSE20650	170247242	170247620	378	11790
Oct1	H2O2-Hela	GSE14283	170239421	170239447	26	19787
Oct1	Hela	GSE14283	170239418	170239453	35	19785
P300	T30-glioblastoma	GSE21026	170258583	170259804	1221	27
PHF8	Hs68plusFBS	GSE20725	170258460	170259975	1515	3
Rb	Senescent	GSE19898	170258940	170259394	454	54
Rb	shRbSenescence	GSE19898	170258971	170259439	468	16
p130	Quiescent	GSE19898	170258663	170259323	660	228
p130	Senescent	GSE19898	170258590	170259232	642	310
p130	shRbQuiescent	GSE19898	170258544	170259353	809	272

Transcrip Factors	Experimental Cell	Database	TF Binding Start	TF Binding End	TF Binding Length	The Distance to Gene
CTCF	G2	GSE9613	170259034	170259414	380	0
FoxA1	MCF7	MACSdata	170260509	170260785	276	0
PHF8	HeLa	GSE20725	170258876	170259803	927	0
p130	Quiescent	GSE19898	170259372	170259684	312	0
p130	shRbSenescent	GSE19898	170258584	170259866	1282	0

Validated miRNA targets

Cis-Nats regulation

Simple Query:

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

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