Identity
HGNC
LOCATION
3q21.3
LOCUSID
ALIAS
NOV,NOVP,PLEXIN-A1,PLXN1
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: 5361
MIM: 601055
HGNC: 9099
Ensembl: ENSG00000114554
Variants:
dbSNP: 5361
ClinVar: 5361
TCGA: ENSG00000114554
COSMIC: PLXNA1
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000114554 | ENST00000393409 | Q9UIW2 |
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 38331165 | 2024 | Chronic stress promotes gastric cancer progression via the adrenoceptor beta 2/PlexinA1 pathway. | 0 |
| 38508474 | 2024 | PlexinA1 promotes gastric cancer migration through preventing MICAL1 protein ubiquitin/proteasome-mediated degradation in a Rac1-dependent manner. | 0 |
| 38331165 | 2024 | Chronic stress promotes gastric cancer progression via the adrenoceptor beta 2/PlexinA1 pathway. | 0 |
| 38508474 | 2024 | PlexinA1 promotes gastric cancer migration through preventing MICAL1 protein ubiquitin/proteasome-mediated degradation in a Rac1-dependent manner. | 0 |
| 38081609 | 2023 | [PLXNA1 is highly expressed in hepatocellular carcinoma and affects patients' survival and immune microenvironment]. | 0 |
| 38081609 | 2023 | [PLXNA1 is highly expressed in hepatocellular carcinoma and affects patients' survival and immune microenvironment]. | 0 |
| 35852441 | 2022 | Rare variant screening and burden analysis of PLXNA1 in Parkinson's disease. | 0 |
| 35852441 | 2022 | Rare variant screening and burden analysis of PLXNA1 in Parkinson's disease. | 0 |
| 34054129 | 2021 | Biallelic and monoallelic variants in PLXNA1 are implicated in a novel neurodevelopmental disorder with variable cerebral and eye anomalies. | 19 |
| 34636164 | 2021 | Analysis of PLXNA1, NRP1, and NRP2 variants in a cohort of patients with isolated hypogonadotropic hypogonadism. | 3 |
| 34054129 | 2021 | Biallelic and monoallelic variants in PLXNA1 are implicated in a novel neurodevelopmental disorder with variable cerebral and eye anomalies. | 19 |
| 34636164 | 2021 | Analysis of PLXNA1, NRP1, and NRP2 variants in a cohort of patients with isolated hypogonadotropic hypogonadism. | 3 |
| 30467832 | 2019 | Prevalence and associated phenotypes of PLXNA1 variants in normosmic and anosmic idiopathic hypogonadotropic hypogonadism. | 13 |
| 30467832 | 2019 | Prevalence and associated phenotypes of PLXNA1 variants in normosmic and anosmic idiopathic hypogonadotropic hypogonadism. | 13 |
| 29091353 | 2018 | Fyn-dependent phosphorylation of PlexinA1 and PlexinA2 at conserved tyrosines is essential for zebrafish eye development. | 7 |
Citation
Dessen P
PLXNA1 (plexin A1)
Atlas Genet Cytogenet Oncol Haematol. 2007-02-01
Online version: http://atlasgeneticsoncology.org/gene/45685/plxna1-(plexin-a1)
