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: 81693
MIM: 605799
HGNC: 14604
Ensembl: ENSG00000166126
Variants:
dbSNP: 81693
ClinVar: 81693
TCGA: ENSG00000166126
COSMIC: AMN
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000166126 | ENST00000299155 | Q9BXJ7 |
| ENSG00000166126 | ENST00000559525 | H0YMX8 |
| ENSG00000166126 | ENST00000559789 | H0YKJ5 |
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 32045704 | 2020 | Imerslund-Gräsbeck Syndrome presenting with microangiopathic hemolytic anemia in a child. | 2 |
| 32045704 | 2020 | Imerslund-Gräsbeck Syndrome presenting with microangiopathic hemolytic anemia in a child. | 2 |
| 29402915 | 2018 | Amnionless-mediated glycosylation is crucial for cell surface targeting of cubilin in renal and intestinal cells. | 17 |
| 30523278 | 2018 | Structural assembly of the megadalton-sized receptor for intestinal vitamin B(12) uptake and kidney protein reabsorption. | 20 |
| 29402915 | 2018 | Amnionless-mediated glycosylation is crucial for cell surface targeting of cubilin in renal and intestinal cells. | 17 |
| 30523278 | 2018 | Structural assembly of the megadalton-sized receptor for intestinal vitamin B(12) uptake and kidney protein reabsorption. | 20 |
| 26040326 | 2015 | Novel compound heterozygous mutations in AMN cause Imerslund-Gräsbeck syndrome in two half-sisters: a case report. | 7 |
| 26040326 | 2015 | Novel compound heterozygous mutations in AMN cause Imerslund-Gräsbeck syndrome in two half-sisters: a case report. | 7 |
| 22929189 | 2012 | Inherited cobalamin malabsorption. Mutations in three genes reveal functional and ethnic patterns. | 21 |
| 22929189 | 2012 | Inherited cobalamin malabsorption. Mutations in three genes reveal functional and ethnic patterns. | 21 |
| 21750092 | 2011 | Luminal expression of cubilin is impaired in Imerslund-Grasbeck syndrome with compound AMN mutations in intron 3 and exon 7. | 10 |
| 22078000 | 2011 | Ancient founder mutation is responsible for Imerslund-Gräsbeck Syndrome among diverse ethnicities. | 8 |
| 21750092 | 2011 | Luminal expression of cubilin is impaired in Imerslund-Grasbeck syndrome with compound AMN mutations in intron 3 and exon 7. | 10 |
| 22078000 | 2011 | Ancient founder mutation is responsible for Imerslund-Gräsbeck Syndrome among diverse ethnicities. | 8 |
| 17979745 | 2007 | Multiligand endocytosis and congenital defects: roles of cubilin, megalin and amnionless. | 20 |
Citation
Dessen P
AMN (amnion associated transmembrane protein)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/60277/gene-fusions-explorer/
