Identity
HGNC
LOCATION
15q11.2
LOCUSID
ALIAS
FSP3,SLC57A1,SPG6
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: 123606
MIM: 608145
HGNC: 17043
Ensembl: ENSG00000170113
Variants:
dbSNP: 123606
ClinVar: 123606
TCGA: ENSG00000170113
COSMIC: NIPA1
RNA/Proteins
Expression (GTEx)
Pathways
| Pathway | Source | External ID |
|---|---|---|
| Transmembrane transport of small molecules | REACTOME | R-HSA-382551 |
| Miscellaneous transport and binding events | REACTOME | R-HSA-5223345 |
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 38667292 | 2024 | Investigating Repeat Expansions in NIPA1, NOP56, and NOTCH2NLC Genes: A Closer Look at Amyotrophic Lateral Sclerosis Patients from Southern Italy. | 0 |
| 38667292 | 2024 | Investigating Repeat Expansions in NIPA1, NOP56, and NOTCH2NLC Genes: A Closer Look at Amyotrophic Lateral Sclerosis Patients from Southern Italy. | 0 |
| 36607129 | 2023 | Clinical and genetic characterization of NIPA1 mutations in a Taiwanese cohort with hereditary spastic paraplegia. | 1 |
| 36736696 | 2023 | LncRNA NIPA1-SO confers atherosclerotic protection by suppressing the transmembrane protein NIPA1. | 2 |
| 36607129 | 2023 | Clinical and genetic characterization of NIPA1 mutations in a Taiwanese cohort with hereditary spastic paraplegia. | 1 |
| 36736696 | 2023 | LncRNA NIPA1-SO confers atherosclerotic protection by suppressing the transmembrane protein NIPA1. | 2 |
| 30342764 | 2019 | Association of NIPA1 repeat expansions with amyotrophic lateral sclerosis in a large international cohort. | 18 |
| 31286297 | 2019 | Analysis of the GCG repeat length in NIPA1 gene in C9orf72-mediated ALS in a large Italian ALS cohort. | 5 |
| 30342764 | 2019 | Association of NIPA1 repeat expansions with amyotrophic lateral sclerosis in a large international cohort. | 18 |
| 31286297 | 2019 | Analysis of the GCG repeat length in NIPA1 gene in C9orf72-mediated ALS in a large Italian ALS cohort. | 5 |
| 29715457 | 2018 | SPG6 supports development of acute myeloid leukemia by regulating BMPR2-Smad-Bcl-2/Bcl-xl signaling. | 2 |
| 29715457 | 2018 | SPG6 supports development of acute myeloid leukemia by regulating BMPR2-Smad-Bcl-2/Bcl-xl signaling. | 2 |
| 26777436 | 2016 | Large-scale screening in sporadic amyotrophic lateral sclerosis identifies genetic modifiers in C9orf72 repeat carriers. | 13 |
| 27084228 | 2016 | Genetic background of the hereditary spastic paraplegia phenotypes in Hungary - An analysis of 58 probands. | 11 |
| 26777436 | 2016 | Large-scale screening in sporadic amyotrophic lateral sclerosis identifies genetic modifiers in C9orf72 repeat carriers. | 13 |
Citation
Dessen P
NIPA1 (NIPA magnesium transporter 1)
Atlas Genet Cytogenet Oncol Haematol. 2018-11-01
Online version: http://atlasgeneticsoncology.org/gene/57706/nipa1-(nipa-magnesium-transporter-1)
