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2158 F9

2158

F9

coagulation factor IX

protein-coding

Homo sapiens

基因描述

Type Description
Definition coagulation factor IX

研究结论

Date Results Publications
2021-04-13 10:15:00 Factor VIII-driven changes in activated factor IX explored by hydrogen-deuterium exchange mass spectrometry. 32678887
2021-04-03 13:38:00 Molecular characterization of hemophilia B patients in Colombia. 32155688
2021-03-27 14:42:00 Progressive increase in FIX level in males with haemophilia B Leyden and c.35G > A mutation in early childhood not related to androgen effect. 32346856
2020-11-21 13:12:00 Hemophilia A and B mice, but not VWF(-/-)mice, display bone defects in congenital development and remodeling after injury. 31594977
2020-07-25 12:00:00 novel mutation of F9 which lead to a premature stop codon at amino acid position 327, it may have an influence on protein characteristics and cause the corresponding disease 31815744

名称对应

Type IDs
Synonymous F9 p22, FIX, HEMB, P19, PTC, THPH8
Gene
UniProtKB-ID: FA9_HUMAN
UniprotKB: P00740
UniParc: UPI00004CA0ED, UPI000002BA13
EMBL: CH471150, AL033403, AF536327, K02402, M11309, M35672, K02052, AB186358, J00137, BC109214, S68634, K02048, S66752, M19063, J00136, K02051, FR846239, BC109215, AK292749, K02049, K02053
Ensembl: ENSG00000101981
KO: hsa:2158
Nucleutide sequences
EMBL-CDS: AAA98726.1, AAA52023.1, AAI09216.1, EAW88433.1, AAA56822.1, AAB59620.1, AAB29758.1, BAD89383.1, AAA52456.1, CCA61111.1, AAB28588.1, AAA51981.1, AAI09215.1, BAF85438.1, AAM96188.1, AAA52763.1
Ensembl_TRS: ENST00000218099, ENST00000394090
Protein sequencees
Ensembl_PRO: ENSP00000377650, ENSP00000218099
RefSeq: NP_001300842.1, XP_005262454.1, NP_000124.1
Others
UniRef100: UniRef100_P00740
UniRef90: UniRef90_P00740
UniRef50: UniRef50_P00740
UniGene: Hs.522798
CCDS: CCDS14666.1, CCDS83495.1

全选

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