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: 3097
MIM: 143054
HGNC: 4921
Ensembl: ENSG00000010818
Variants:
dbSNP: 3097
ClinVar: 3097
TCGA: ENSG00000010818
COSMIC: HIVEP2
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000010818 | ENST00000012134 | P31629 |
| ENSG00000010818 | ENST00000367603 | P31629 |
| ENSG00000010818 | ENST00000367604 | P31629 |
Expression (GTEx)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 32680547 | 2020 | Nuclear factor kappa B activation appears weaker in schizophrenia patients with high brain cytokines than in non-schizophrenic controls with high brain cytokines. | 19 |
| 32680547 | 2020 | Nuclear factor kappa B activation appears weaker in schizophrenia patients with high brain cytokines than in non-schizophrenic controls with high brain cytokines. | 19 |
| 30682089 | 2019 | HIV-1 infection increases microRNAs that inhibit Dicer1, HRB and HIV-EP2, thereby reducing viral replication. | 20 |
| 31207095 | 2019 | Expanding the phenotype of intellectual disability caused by HIVEP2 variants. | 6 |
| 31586043 | 2019 | Identification of HIVEP2 as a dopaminergic transcription factor related to substance use disorders in rats and humans. | 4 |
| 30682089 | 2019 | HIV-1 infection increases microRNAs that inhibit Dicer1, HRB and HIV-EP2, thereby reducing viral replication. | 20 |
| 31207095 | 2019 | Expanding the phenotype of intellectual disability caused by HIVEP2 variants. | 6 |
| 31586043 | 2019 | Identification of HIVEP2 as a dopaminergic transcription factor related to substance use disorders in rats and humans. | 4 |
| 26153216 | 2016 | Loss-of-function variants in HIVEP2 are a cause of intellectual disability. | 20 |
| 27003583 | 2016 | Mutations in HIVEP2 are associated with developmental delay, intellectual disability, and dysmorphic features. | 21 |
| 26153216 | 2016 | Loss-of-function variants in HIVEP2 are a cause of intellectual disability. | 20 |
| 27003583 | 2016 | Mutations in HIVEP2 are associated with developmental delay, intellectual disability, and dysmorphic features. | 21 |
| 22294689 | 2012 | Genome-wide repression of NF-κB target genes by transcription factor MIBP1 and its modulation by O-linked β-N-acetylglucosamine (O-GlcNAc) transferase. | 9 |
| 22294689 | 2012 | Genome-wide repression of NF-κB target genes by transcription factor MIBP1 and its modulation by O-linked β-N-acetylglucosamine (O-GlcNAc) transferase. | 9 |
| 22294689 | 2012 | Genome-wide repression of NF-κB target genes by transcription factor MIBP1 and its modulation by O-linked β-N-acetylglucosamine (O-GlcNAc) transferase. | 9 |
Citation
Dessen P
HIVEP2 (HIVEP zinc finger 2)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/64327/hivep2-(hivep-zinc-finger-2)
