FOXN1
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 17[11]
- Cytogenetic location
- 17q11.2[14]
- Encodes
- Forkhead box N1[9]
- Expressed in
- gingival epithelium, skin of thigh, skin of abdomen, human penis, skin of hip, vulva, nipple, oral cavity, mucosa of pharynx, vagina[15][16][17][18][19][20][21][22][23][24]
- Found in taxon
- Homo sapiens[10]
- Genetic association
- T-cell immunodeficiency, congenital alopecia, and nail dystrophy[12]
- HomoloGene ID
- 2664[3]
- Strand orientation
- forward strand[13]
🏷️ Also known as
en WHN
en FKHL20
en forkhead box N1
en FOXN1
en RONU
en TIDAND
en TLIND
ar FOXN١
🔖 Identifiers · 11
- Ensembl gene ID
- ENSG00000109101
- Ensembl transcript ID
- ENST00000579795, ENST00000226247, ENST00000577936
- Entrez Gene ID
- 8456
- Exact match
- identifiers.org
- Freebase ID
- /m/03m7zrf
- HGNC ID
- 12765
- HGNC gene symbol
- FOXN1
- Microsoft Academic ID (discontinued)
- 2779746258
- OMIM ID
- 600838
- RefSeq RNA ID
- XM_011525370, NM_003593, XM_011525358, XM_011525359, XM_011525362, XM_011525367, XM_011525368, XM_011525369, XM_017025229, XM_017025230, XM_017025231, NM_001369369, XM_047436939
- UMLS CUI
- C1421504
🔗 Connections
Expressed in 4
Chromosome 1
Found in taxon 1
Instance of 1
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