InnateDB Protein
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IDBP-762984.3
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Last Modified
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2014-10-13 [Report errors or provide feedback]
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Gene Symbol
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FOXN1
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Protein Name
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Synonyms
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FKHL20; RONU; WHN;
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Species
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Homo sapiens
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Ensembl Protein
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ENSP00000464645
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InnateDB Gene
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IDBG-36752 (FOXN1)
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Protein Structure
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Function |
Transcriptional regulator involved in development.
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Subcellular Localization |
Nucleus.
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Disease Associations |
T-cell immunodeficiency, congenital alopecia, and nail dystrophy (TIDAND) [MIM:601705]: A disorder characterized by the association of congenital alopecia, severe T-cell immunodeficiency, and ridging and pitting of all nails. {ECO:0000269PubMed:10206641}. Note=The disease is caused by mutations affecting the gene represented in this entry.
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Tissue Specificity |
Expressed in thymus.
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Comments |
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Number of Interactions
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This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
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Molecular Function |
Accession |
GO Term |
GO:0003700
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sequence-specific DNA binding transcription factor activity
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GO:0043565
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sequence-specific DNA binding
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Biological Process |
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Cellular Component |
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PDB ID |
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InterPro |
IPR001766
Transcription factor, fork head
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PFAM |
PF00250
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PRINTS |
PR00053
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PIRSF |
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SMART |
SM00339
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TIGRFAMs |
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Modification |
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SwissProt |
O15353
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PhosphoSite |
PhosphoSite-O15353
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TrEMBL |
J3KRT9
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UniProt Splice Variant |
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Entrez Gene |
8456
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UniGene |
Hs.663679
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RefSeq |
XP_005258103
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HUGO |
HGNC:12765
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OMIM |
600838
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CCDS |
CCDS11232
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HPRD |
02907
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IMGT |
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EMBL |
AC005726
AC015917
AK313878
CH471159
Y11739
Y11741
Y11742
Y11743
Y11744
Y11745
Y11746
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GenPept |
BAG36604
CAA72416
CAA72417
EAW51092
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