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197257 LDHD

197257

LDHD

lactate dehydrogenase D

protein-coding

Homo sapiens

基因描述

Type Description
Definition lactate dehydrogenase D

研究结论

Date Results Publications
2020-06-27 11:09:00 gout can be caused by a mutation in LDHD within the putative catalytic site of the encoded d-lactate dehydrogenase, resulting in augmented blood levels of d-lactate, a stereoisomer of l-lactate 31638601
2013-04-13 11:30:00 The activity and expression of the mitochondrial D-lactate dehydrogenase, is higher in prostate cancer versus normal prostate cells. 23333299
2011-02-26 10:06:00 Elevated serum LDH isoenzymes and AST indicate a disturbance (of uncertain clinical significance) within multiple extraosseous tissues when there is CLCN7 deficiency. 20499337
2010-12-05 22:08:00 Observational study of gene-disease association. (HuGE Navigator) 20877624
2010-01-21 00:00:00 identification and characterization of human and mouse D-lactate dehydrogenase (NAD) [D-LDH] 12127981

名称对应

Type IDs
Synonymous DLD
Gene
UniProtKB-ID: LDHD_HUMAN
UniprotKB: Q86WU2
UniParc: UPI0000062302, UPI0000051E1F
EMBL: BC040279, BC047902, AY092767
Ensembl: ENSG00000166816
KO: hsa:197257
Nucleutide sequences
EMBL-CDS: AAH40279.1, AAH47902.1, AAM50322.1
Ensembl_TRS: ENST00000300051, ENST00000450168
Protein sequencees
Ensembl_PRO: ENSP00000417011, ENSP00000300051
RefSeq: NP_705690.2, XP_024305945.1, XP_024305943.1, XP_024305944.1, NP_919417.1, XP_024305947.1, XP_024305946.1, XP_024305942.1
Others
UniRef100: UniRef100_Q86WU2
UniRef90: UniRef90_Q86WU2
UniRef50: UniRef50_Q86WU2
UniGene: Hs.380929
CCDS: CCDS10913.1, CCDS45529.1

全选

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