Identity
HGNC
LOCATION
18p11.31
LOCUSID
ALIAS
LAMA,PTBHS,S-LAM-alpha
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: 284217
MIM: 150320
HGNC: 6481
Ensembl: ENSG00000101680
Variants:
dbSNP: 284217
ClinVar: 284217
TCGA: ENSG00000101680
COSMIC: LAMA1
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000101680 | ENST00000389658 | P25391 |
| ENSG00000101680 | ENST00000638611 | A0A1W2PQN4 |
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 35616092 | 2022 | Variability of retinopathy consequent upon novel mutations in LAMA1. | 0 |
| 35616092 | 2022 | Variability of retinopathy consequent upon novel mutations in LAMA1. | 0 |
| 33513766 | 2021 | Spermatogonia Loss Correlates with LAMA 1 Expression in Human Prepubertal Testes Stored for Fertility Preservation. | 12 |
| 34226522 | 2021 | Circular RNA hsa_circ_0000277 sequesters miR-4766-5p to upregulate LAMA1 and promote esophageal carcinoma progression. | 27 |
| 33513766 | 2021 | Spermatogonia Loss Correlates with LAMA 1 Expression in Human Prepubertal Testes Stored for Fertility Preservation. | 12 |
| 34226522 | 2021 | Circular RNA hsa_circ_0000277 sequesters miR-4766-5p to upregulate LAMA1 and promote esophageal carcinoma progression. | 27 |
| 32072250 | 2020 | Organisation of extracellular matrix proteins laminin and agrin in pericapillary basal laminae in mouse brain. | 9 |
| 32072250 | 2020 | Organisation of extracellular matrix proteins laminin and agrin in pericapillary basal laminae in mouse brain. | 9 |
| 31183318 | 2019 | The Laminin-α1 Chain-Derived Peptide, AG73, Binds to Syndecans on MDA-231 Breast Cancer Cells and Alters Filopodium Formation. | 3 |
| 31183318 | 2019 | The Laminin-α1 Chain-Derived Peptide, AG73, Binds to Syndecans on MDA-231 Breast Cancer Cells and Alters Filopodium Formation. | 3 |
| 28544784 | 2017 | Presynaptic congenital myasthenic syndrome with a homozygous sequence variant in LAMA5 combines myopia, facial tics, and failure of neuromuscular transmission. | 16 |
| 28544784 | 2017 | Presynaptic congenital myasthenic syndrome with a homozygous sequence variant in LAMA5 combines myopia, facial tics, and failure of neuromuscular transmission. | 16 |
| 26215696 | 2016 | Biophysical analysis of a lethal laminin alpha-1 mutation reveals altered self-interaction. | 6 |
| 26862816 | 2016 | Effect of a Single Nucleotide Polymorphism in the LAMA1 Promoter Region on Transcriptional Activity: Implication for Pathological Myopia. | 5 |
| 26932191 | 2016 | Clinical, neuroradiological and molecular characterization of cerebellar dysplasia with cysts (Poretti-Boltshauser syndrome). | 12 |
Citation
Dessen P
LAMA1 (laminin subunit alpha 1)
Atlas Genet Cytogenet Oncol Haematol. 2009-09-01
Online version: http://atlasgeneticsoncology.org/gene/51060/
