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.

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Pathways reviewed by Belaya, Katsiaryna (5633214)

DB_ID Name
4549349 Defective ALG2 causes ALG2-CDG (CDG-1i)
4549356 Defective DPAGT1 causes DPAGT1-CDG (CDG-1j) and CMSTA2
4549380 Defective ALG1 causes ALG1-CDG (CDG-1k)
4551295 Defective ALG11 causes ALG11-CDG (CDG-1p)
4570571 Defective RFT1 causes RFT1-CDG (CDG-1n)
5633231 Defective ALG14 causes congenital myasthenic syndrome (ALG14-CMS)
4687000 Defective MPDU1 causes MPDU1-CDG (CDG-1f)
4720454 Defective ALG9 causes ALG9-CDG (CDG-1l)
4720475 Defective ALG3 causes ALG3-CDG (CDG-1d)
4720489 Defective ALG12 causes ALG12-CDG (CDG-1g)
4724289 Defective ALG6 causes ALG6-CDG (CDG-1c)
4724325 Defective ALG8 causes ALG8-CDG (CDG-1h)
4793950 Defective MAN1B1 causes MRT15
4793953 Defective B4GALT1 causes B4GALT1-CDG (CDG-2d)
4793952 Defective MGAT2 causes MGAT2-CDG (CDG-2a)
4793954 Defective MOGS causes MOGS-CDG (CDG-2b)
3781860 Diseases associated with N-glycosylation of proteins

Details on Person Belaya, Katsiaryna

Class:IdPerson:5633214
_displayNameBelaya, Katsiaryna
_timestamp2017-08-22 20:40:47
created[InstanceEdit:5633234] Jassal, Bijay, 2014-10-31
firstnameKatsiaryna
initialK
modified[InstanceEdit:5634130] Jassal, Bijay, 2014-11-03
[InstanceEdit:5637452] Jassal, Bijay, 2014-11-10
surnameBelaya
(author)[InstanceEdit:5633220] Belaya, Katsiaryna, 2014-10-31
[LiteratureReference:4549335] Mutations in DPAGT1 cause a limb-girdle congenital myasthenic syndrome with tubular aggregates
[LiteratureReference:5633222] Congenital myasthenic syndromes due to mutations in ALG2 and ALG14
[LiteratureReference:5633243] Clinical features of congenital myasthenic syndrome due to mutations in DPAGT1
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