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: 8456
MIM: 600838
HGNC: 12765
Ensembl: ENSG00000109101
Variants:
dbSNP: 8456
ClinVar: 8456
TCGA: ENSG00000109101
COSMIC: FOXN1
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000109101 | ENST00000226247 | O15353 |
| ENSG00000109101 | ENST00000577936 | J3KRT9 |
| ENSG00000109101 | ENST00000579795 | O15353 |
Expression (GTEx)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 36631020 | 2023 | [Effects of FoxN1, p63 and AIRE on the process of age-related thymus involution: An update]. | 0 |
| 37419334 | 2023 | Comprehensive phenotypic analysis of diverse FOXN1 variants. | 2 |
| 36631020 | 2023 | [Effects of FoxN1, p63 and AIRE on the process of age-related thymus involution: An update]. | 0 |
| 37419334 | 2023 | Comprehensive phenotypic analysis of diverse FOXN1 variants. | 2 |
| 35527675 | 2022 | Expression of BMP4 and FOXN1 in orthokeratinized odontogenic cyst compared to odontogenic keratocyst suggests an epidermal phenotype. | 1 |
| 35527675 | 2022 | Expression of BMP4 and FOXN1 in orthokeratinized odontogenic cyst compared to odontogenic keratocyst suggests an epidermal phenotype. | 1 |
| 33464451 | 2021 | Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations. | 13 |
| 33464451 | 2021 | Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations. | 13 |
| 31914405 | 2020 | The crystal structure of human forkhead box N1 in complex with DNA reveals the structural basis for forkhead box family specificity. | 14 |
| 31914405 | 2020 | The crystal structure of human forkhead box N1 in complex with DNA reveals the structural basis for forkhead box family specificity. | 14 |
| 31447097 | 2019 | Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis. | 37 |
| 31566583 | 2019 | FOXN1 compound heterozygous mutations cause selective thymic hypoplasia in humans. | 26 |
| 31447097 | 2019 | Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis. | 37 |
| 31566583 | 2019 | FOXN1 compound heterozygous mutations cause selective thymic hypoplasia in humans. | 26 |
| 28636882 | 2017 | FOXN1 Italian founder mutation in Indian family: Implications in prenatal diagnosis. | 11 |
Citation
Dessen P
FOXN1 (forkhead box N1)
Atlas Genet Cytogenet Oncol Haematol. 2007-04-01
Online version: http://atlasgeneticsoncology.org/gene/46997/foxn1-(forkhead-box-n1)
