Reactome: A Curated Pathway Database

Query author contributions in Reactome

Reactome depends on collaboration between our curation team and outside experts to assemble and peer-review its pathway modules. The integration of ORCID within Reactome enables us to meet a key challenge with authoring, curating and reviewing biological information by incentivizing and crediting the external experts that contribute their expertise and time to the Reactome curation process. More information is available at ORCID and Reactome.

If you have an ORCID ID that is not listed on this page, please forward this information to us and we will update your Reactome pathway records.

Name Email address

Pathways reviewed by Nakaki, Toshio (5634118)

DB_ID Name
5578997 Defective AHCY causes Hypermethioninemia with S-adenosylhomocysteine hydrolase deficiency (HMAHCHD)
5578996 Defective CYP27A1 causes Cerebrotendinous xanthomatosis (CTX)
5578999 Defective GCLC causes Hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency (HAGGSD)
5578998 Defective OPLAH causes 5-oxoprolinase deficiency (OPLAHD)
5578995 Defective TPMT causes Thiopurine S-methyltransferase deficiency (TPMT deficiency)
5579005 Defective CYP4F22 causes Ichthyosis, congenital, autosomal recessive 5 (ARCI5)
5579004 Defective CYP26C1 causes Focal facial dermal dysplasia 4 (FFDD4)
5579007 Defective ACY1 causes encephalopathy
5579006 Defective GSS causes Glutathione synthetase deficiency (GSS deficiency)
5579000 Defective CYP1B1 causes Glaucoma
5579002 Defective UGT1A1 causes hyperbilirubinemia
5579029 Metabolic disorders of biological oxidation enzymes
5579028 Defective CYP17A1 causes Adrenal hyperplasia 5 (AH5)
5579031 Defective ACTH causes Obesity and Pro-opiomelanocortinin deficiency (POMCD)
5579030 Defective CYP19A1 causes Aromatase excess syndrome (AEXS)
5579024 Defective MAT1A causes Methionine adenosyltransferase deficiency (MATD)
5579027 Defective CYP2R1 causes Rickets vitamin D-dependent 1B (VDDR1B)
5579026 Defective CYP11A1 causes Adrenal insufficiency, congenital, with 46,XY sex reversal (AICSR)
5579032 Defective TBXAS1 causes Ghosal hematodiaphyseal dysplasia (GHDD)
5579013 Defective CYP7B1 causes Spastic paraplegia 5A, autosomal recessive (SPG5A) and Congenital bile acid synthesis defect 3 (CBAS3)
5579012 Defective MAOA causes Brunner syndrome (BRUNS)
5579015 Defective CYP26B1 causes Radiohumeral fusions with other skeletal and craniofacial anomalies (RHFCA)
5579014 Defective CYP27B1 causes Rickets vitamin D-dependent 1A (VDDR1A)
5579009 Defective CYP11B2 causes Corticosterone methyloxidase 1 deficiency (CMO-1 deficiency)
5579011 Defective CYP2U1 causes Spastic paraplegia 56, autosomal recessive (SPG56)
5579010 Defective CYP24A1 causes Hypercalcemia, infantile (HCAI)
5579021 Defective CYP21A2 causes Adrenal hyperplasia 3 (AH3)
5579020 Defective SLC35D1 causes Schneckenbecken dysplasia (SCHBCKD)
5579022 Defective GGT1 causes Glutathionuria (GLUTH)
5579017 Defective CYP11B1 causes Adrenal hyperplasia 4 (AH4)
5579016 Defective UGT1A4 causes hyperbilirubinemia
5579019 Defective FMO3 causes Trimethylaminuria (TMAU)

Details on Person Nakaki, Toshio

_displayNameNakaki, Toshio
_timestamp2017-08-22 20:40:49
created[InstanceEdit:5634120] Jassal, Bijay, 2014-11-03
modified[InstanceEdit:5637452] Jassal, Bijay, 2014-11-10
(author)[InstanceEdit:5634119] Nakaki, Toshio, 2014-11-03
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