PHIP

Information PHIP

Description

This gene encodes a protein that binds to the insulin receptor substrate 1 protein and regulates glucose transporter translocation in skeletal muscle cells. The encoded protein may also regulate growth and survival of pancreatic beta cells. Elevated copy number of this gene may be associated with melanoma severity and the encoded protein may promote melanoma metastasis in human patients. [provided by RefSeq, Oct 2016]

Full Name

pleckstrin homology domain interacting protein

Source NCBI

ReMap Statistics

Datasets
8
Biotypes
2
Peaks
428,335
Non-redundant peaks
265,034

TF Classification

Super Class
NA
Class
NA
Familly
NA
Sub Familly
NA

Source TFClass

External IDs

JASPAR
Ensembl
ENSG00000146247
UniProt
Q8WWQ0
Genevisible
Q8WWQ0
RefSeq
NM_017934
Aliases
BRWD2; DCAF14; FLJ20705; ndrp
All peaks PHIP
Download BED file
Non redundant peaks PHIP
Download BED file
SEQUENCES PHIP
Download FASTA file
DOWNLOAD All ReMap
Got to catalogue

Datasets Table for PHIP

Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks
PHIP HEK293 ab833 GEO Homo sapiens GSE101646 67,329
PHIP HEK293 flag_brwd2_phip GEO Homo sapiens GSE101646 147,081
PHIP HCT-116 ab833 GEO Homo sapiens GSE101646 79,635
PHIP HCT-116 ab834 GEO Homo sapiens GSE101646 34,192
PHIP HCT-116 BRWD2-KO_ab833 GEO Homo sapiens GSE101646 1,280
PHIP HCT-116 MLL1-KO__ab833 GEO Homo sapiens GSE101646 67,864
PHIP HCT-116 MLL4-SET-KO_ab833 GEO Homo sapiens GSE101646 17,929
PHIP HCT-116 MLL4-SET-KO_ab834 GEO Homo sapiens GSE101646 13,025
Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks

ReMap is a database of transcriptional regulators peaks derived from curated ChIP-seq, ChIP-exo, DAP-seq experiments in Human and Thaliana.

You are using the 2020 ReMap (3rd) release.
The ReMap catalogues (2020, 2018, 2015) are under CC BY-NC 4.0 international license, while ReMapEnrich, remap-pipeline under GNU GPLv3 licence.

Inserm TAGC
AMU AMU-MESO

This work was granted access to the HPC resources of Aix-Marseille Université financed by the project Equip@Meso (ANR-10-EQPX-29-01) of the program "Investissements d’Avenir" supervised by the Agence Nationale de la Recherche.