Identity
HGNC
LOCATION
1q21.3
LOCUSID
ALIAS
MRD37,WHSUS,ZNF280E,ZNF635,ZNF635m
FUSION GENES
Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 23126
MIM: 614787
HGNC: 18801
Ensembl: ENSG00000143442
Variants:
dbSNP: 23126
ClinVar: 23126
TCGA: ENSG00000143442
COSMIC: POGZ
RNA/Proteins
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 38350721 | 2024 | Exploring the molecular pathways linking sleep phenotypes and POGZ-associated neurodevelopmental disorder. | 0 |
| 38350721 | 2024 | Exploring the molecular pathways linking sleep phenotypes and POGZ-associated neurodevelopmental disorder. | 0 |
| 36658409 | 2023 | Chromodomain on Y-like 2 (CDYL2) implicated in mitosis and genome stability regulation via interaction with CHAMP1 and POGZ. | 1 |
| 36658409 | 2023 | Chromodomain on Y-like 2 (CDYL2) implicated in mitosis and genome stability regulation via interaction with CHAMP1 and POGZ. | 1 |
| 34758190 | 2022 | POGZ promotes homology-directed DNA repair in an HP1-dependent manner. | 7 |
| 35052493 | 2022 | Genotype-Phenotype Comparison in POGZ-Related Neurodevelopmental Disorders by Using Clinical Scoring. | 4 |
| 35367590 | 2022 | Loss of POGZ alters neural differentiation of human embryonic stem cells. | 2 |
| 34758190 | 2022 | POGZ promotes homology-directed DNA repair in an HP1-dependent manner. | 7 |
| 35052493 | 2022 | Genotype-Phenotype Comparison in POGZ-Related Neurodevelopmental Disorders by Using Clinical Scoring. | 4 |
| 35367590 | 2022 | Loss of POGZ alters neural differentiation of human embryonic stem cells. | 2 |
| 33277917 | 2021 | Neuropsychological study in 19 French patients with White-Sutton syndrome and POGZ mutations. | 8 |
| 33726803 | 2021 | Intranasal oxytocin administration ameliorates social behavioral deficits in a POGZ(WT/Q1038R) mouse model of autism spectrum disorder. | 10 |
| 34206215 | 2021 | Adducted Thumb and Peripheral Polyneuropathy: Diagnostic Supports in Suspecting White-Sutton Syndrome: Case Report and Review of the Literature. | 4 |
| 34474553 | 2021 | Identification of abnormally high expression of POGZ as a new biomarker associated with a poor prognosis in osteosarcoma. | 4 |
| 34879283 | 2021 | Autism risk gene POGZ promotes chromatin accessibility and expression of clustered synaptic genes. | 27 |
Citation
Dessen P
POGZ (pogo transposable element derived with ZNF domain)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/72045/pogz-(pogo-transposable-element-derived-with-znf-domain)
