GLIS2

Information GLIS2

Description

This gene is a member of the GLI-similar zinc finger protein family and encodes a nuclear transcription factor with five C2H2-type zinc finger domains. The protein encoded by this gene is widely expressed at low levels in the neural tube and peripheral nervous system and likely promotes neuronal differentiation. It is abundantly expressed in the kidney and may have a role in the regulation of kidney morphogenesis. p120 regulates the expression level of this protein and induces the cleavage of this protein's C-terminal zinc finger domain. This protein also promotes the nuclear translocation of p120. Mutations in this gene cause nephronophthisis (NPHP), an autosomal recessive kidney disease characterized by tubular basement membrane disruption, interstitial lymphohistiocytic cell infiltration, and development of cysts at the corticomedullary border of the kidneys.[provided by RefSeq, Jan 2010]

Full Name

GLIS family zinc finger 2

Source NCBI

ReMap Statistics

Datasets
1
Biotypes
1
Peaks
50,170
Non-redundant peaks
50,170

TF Classification

Super Class
NA
Class
NA
Familly
NA
Sub Familly
NA

Source TFClass

External IDs

JASPAR
MA0736
Ensembl
ENSG00000274636
UniProt
Q9BZE0
Genevisible
Q9BZE0
RefSeq
NM_001318918
Aliases
NPHP7
All peaks GLIS2
Download BED file
Non redundant peaks GLIS2
Download BED file
SEQUENCES GLIS2
Download FASTA file
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Datasets Table for GLIS2

Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks
GLIS2 HEK293 ENCODE Homo sapiens ENCSR535DIA 50,170
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.