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8456 FOXN1

8456

FOXN1

forkhead box N1

protein-coding

Homo sapiens

基因描述

Type Description
Definition forkhead box N1

研究结论

Date Results Publications
2020-10-24 14:03:00 The crystal structure of human forkhead box N1 in complex with DNA reveals the structural basis for forkhead box family specificity. 31914405
2020-06-13 13:05:00 FOXN1 compound heterozygous mutations cause selective thymic hypoplasia in humans. 31566583
2020-04-04 10:44:00 observations establish a FOXN1 gene dosage effect on thymic function and identify FOXN1 haploinsufficiency as an important genetic determinant of T cell lymphopenia at birth. 31447097
2019-03-16 11:04:00 Here, by engineering a time-delayed feedback system of BMP inhibition in mouse embryos, the authors demonstrate that thymopoiesis irreversibly fails if Foxn1 gene expression does not occur during a defining time span in mid-gestation. They also reveal an epistatic interaction between the extent of BMP signalling and the gene dosage of Foxn1. 28819138
2017-09-23 10:33:00 FOXN1 founder Italian mutation identified in an indian newborn with severe combined immunodeficiency. 28636882

名称对应

Type IDs
Synonymous FKHL20, RONU, WHN
Gene
UniProtKB-ID: FOXN1_HUMAN
UniprotKB: O15353
UniParc: UPI000012ADE6
EMBL: Y11744, Y11742, AK313878, Y11743, CH471159, Y11746, Y11741, Y11739, Y11745
Ensembl: ENSG00000109101
KO: hsa:8456
Nucleutide sequences
EMBL-CDS: EAW51092.1, CAA72416.1, BAG36604.1, CAA72417.1
Ensembl_TRS: ENST00000226247, ENST00000579795
Protein sequencees
Ensembl_PRO: ENSP00000464645, ENSP00000226247
RefSeq: XP_016880717.1, XP_011523672.1, XP_011523660.1, NP_003584.2, XP_016880720.1, XP_011523670.1, XP_016880719.1, XP_011523661.1, NP_001356298.1, XP_011523664.1, XP_011523669.1, XP_011523671.1, XP_016880718.1
Others
UniRef100: UniRef100_O15353
UniRef90: UniRef90_O15353
UniRef50: UniRef50_O15353
UniGene: Hs.663679
CCDS: CCDS11232.1

全选

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