Defective SLC6A18 does not transport Gly from extracellular region to cytosol - Wikidata - awgldk - TriplyDB

Defective SLC6A18 does not transport Gly from extracellular region to cytosol

Defective SLC6A18 does not transport Gly from extracellular region to cytosol

http://www.wikidata.org/entity/Q50289049

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Defective SLC6A18 may confer susceptibility to iminoglycinuria and/or hyperglycinuria Defective SLC6A18 may confer susceptibility to iminoglycinuria and/or hyperglycinuria_R-HSA-5619102

P527

Q45315106-BF0B52CF-E52B-4AFB-80B6-43A7415149B4 Q56860920-CA585689-9368-471A-934F-2738A5249F70

P527

Defective SLC6A18 does not transport Gly from extracellular region to cytosol

http://www.wikidata.org/entity/Q50289049

description

An instance of the biological ...... ion to cytosol in Homo sapiens

@en

biologisch proces

@nl

name

Defective SLC6A18 does not transport Gly from extracellular region to cytosol

@en

type

label

Defective SLC6A18 does not transport Gly from extracellular region to cytosol

@en

prefLabel

Defective SLC6A18 does not transport Gly from extracellular region to cytosol

@en

P2860

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P2888

Q50289049-D499A843-4E2E-4616-8C7B-33D6A7CA19E8

P31

Q50289049-48054AA3-E887-4EFB-B36A-529EA25E1C96

P361

Q50289049-30F06235-3912-4B2C-A73B-A55D1EFFD60B

P3937

Q50289049-BCC48425-5405-4799-B487-899A465E85A6

P527

Q50289049-6F35B91A-E21F-4C6C-9361-DCB5F26B9BD6

P703

Q50289049-4B5AEFDE-6479-49DC-A152-88DBDBD8C63F

P2860

Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters

P2888

reactome:R-HSA-5659755

P31

biological process

P361

Defective SLC6A18 may confer susceptibility to iminoglycinuria and/or hyperglycinuria

P3937

R-HSA-5659755

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

P527

P703