Defective MTR does not transfer CH3 group from MTHF to cob(I)alamin - Wikidata - awgldk - TriplyDB

Defective MTR does not transfer CH3 group from MTHF to cob(I)alamin

Defective MTR does not transfer CH3 group from MTHF to cob(I)alamin

http://www.wikidata.org/entity/Q50289126

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Defective MTR causes methylmalonic aciduria and homocystinuria type cblG

P527

Q45316449-621D541B-A917-4158-8EE5-669D673622B3

P527

Defective MTR does not transfer CH3 group from MTHF to cob(I)alamin

http://www.wikidata.org/entity/Q50289126

description

An instance of the biological ...... o cob(I)alamin in Homo sapiens

@en

biologisch proces

@nl

name

Defective MTR does not transfer CH3 group from MTHF to cob(I)alamin

@en

type

label

Defective MTR does not transfer CH3 group from MTHF to cob(I)alamin

@en

prefLabel

Defective MTR does not transfer CH3 group from MTHF to cob(I)alamin

@en

P2860

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Q50289126-B67F55FA-84B1-4D0A-8A65-D608D05BCE04

P2888

Q50289126-E6F5C30F-DB47-4821-9882-68A8144BFF2A

P31

Q50289126-EE51F436-2C14-4BDA-BDC4-87B3B8E025B0

P361

Q50289126-B8FF7126-3615-4726-8240-0701FA98D9E5

P3937

Q50289126-427ABE48-EEE4-4D7E-BAF8-AA0F926ABF8F

P527

Q50289126-168415F2-CAD0-4AE1-8B0D-BC8A0FA51411

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P703

Q50289126-B8786F6D-A8B0-4DF3-B3A1-7B684FDBA306

P2860

Human methionine synthase: cDNA cloning and identification of mutations in patients of the cblG complementation group of folate/cobalamin disorders

Hyperhomocysteinemia due to methionine synthase deficiency, cblG: structure of the MTR gene, genotype diversity, and recognition of a common mutation, P1173L

Defects in human methionine synthase in cblG patients

P2888

reactome:R-HSA-3321918

P31

biological process

P361

Defective MTR causes methylmalonic aciduria and homocystinuria type cblG

P3937

R-HSA-3321918

http://www.w3.org/2001/XMLSchema#string

P527

levomefolic acid

MTRR:mutant MTR(cob(I)alamin)

P703