Identity
HGNC
LOCATION
1q23.3
LOCUSID
ALIAS
DFNA7,LMX1,LMX1.1
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: 4009
MIM: 600298
HGNC: 6653
Ensembl: ENSG00000162761
Variants:
dbSNP: 4009
ClinVar: 4009
TCGA: ENSG00000162761
COSMIC: LMX1A
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000162761 | ENST00000294816 | Q8TE12 |
| ENSG00000162761 | ENST00000342310 | Q8TE12 |
| ENSG00000162761 | ENST00000367893 | Q8TE12 |
Expression (GTEx)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 38759646 | 2024 | Forced LMX1A expression induces dorsal neural fates and disrupts patterning of human embryonic stem cells into ventral midbrain dopaminergic neurons. | 0 |
| 38759646 | 2024 | Forced LMX1A expression induces dorsal neural fates and disrupts patterning of human embryonic stem cells into ventral midbrain dopaminergic neurons. | 0 |
| 35254497 | 2022 | Update on CD164 and LMX1A genes to strengthen their causative role in autosomal dominant hearing loss. | 4 |
| 35711095 | 2022 | Novel Molecular Genetic Etiology of Asymmetric Hearing Loss: Autosomal-Dominant LMX1A Variants. | 6 |
| 36197580 | 2022 | ceRNA network of lncRNA MIR210HG/miR-377-3p/LMX1A in malignant proliferation of glioma cells. | 2 |
| 35254497 | 2022 | Update on CD164 and LMX1A genes to strengthen their causative role in autosomal dominant hearing loss. | 4 |
| 35711095 | 2022 | Novel Molecular Genetic Etiology of Asymmetric Hearing Loss: Autosomal-Dominant LMX1A Variants. | 6 |
| 36197580 | 2022 | ceRNA network of lncRNA MIR210HG/miR-377-3p/LMX1A in malignant proliferation of glioma cells. | 2 |
| 32207384 | 2020 | Circular RNA circMTO1 Suppresses RCC Cancer Cell Progression via miR9/LMX1A Axis. | 6 |
| 32751497 | 2020 | Epigenetic Silencing of LMX1A Contributes to Cancer Progression in Lung Cancer Cells. | 5 |
| 32840933 | 2020 | Novel genotype-phenotype correlation of functionally characterized LMX1A variants linked to sensorineural hearing loss. | 7 |
| 32207384 | 2020 | Circular RNA circMTO1 Suppresses RCC Cancer Cell Progression via miR9/LMX1A Axis. | 6 |
| 32751497 | 2020 | Epigenetic Silencing of LMX1A Contributes to Cancer Progression in Lung Cancer Cells. | 5 |
| 32840933 | 2020 | Novel genotype-phenotype correlation of functionally characterized LMX1A variants linked to sensorineural hearing loss. | 7 |
| 30377043 | 2019 | Gene variations in PBX1, LMX1A and SLITRK1 are associated with obsessive-compulsive disorder and its clinical features. | 4 |
Citation
Dessen P
LMX1A (LIM homeobox transcription factor 1 alpha)
Atlas Genet Cytogenet Oncol Haematol. 2011-03-01
Online version: http://atlasgeneticsoncology.org/gene/52143/lmx1a-(lim-homeobox-transcription-factor-1-alpha)
