Defective SLC22A18 does not exchange extracellular organic cations for cytosolic H+ - Wikidata - wikimedia - TriplyDB

Defective SLC22A18 does not exchange extracellular organic cations for cytosolic H+

Defective SLC22A18 does not exchange extracellular organic cations for cytosolic H+

http://www.wikidata.org/entity/Q50289006

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Defective SLC22A18 causes lung cancer (LNCR) and embryonal rhabdomyosarcoma 1 (RMSE1)

P527

Q45314493-EFA713A9-5131-436C-8039-338E7F362243

P527

Defective SLC22A18 does not exchange extracellular organic cations for cytosolic H+

http://www.wikidata.org/entity/Q50289006

description

An instance of the biological ...... r cytosolic H+ in Homo sapiens

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biologisch proces

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name

Defective SLC22A18 does not exchange extracellular organic cations for cytosolic H+

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type

label

Defective SLC22A18 does not exchange extracellular organic cations for cytosolic H+

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prefLabel

Defective SLC22A18 does not exchange extracellular organic cations for cytosolic H+

@en

P2860

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Q50289006-47D08BB4-3100-446F-A394-86291758E1EF

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Q50289006-8B534522-601C-4A3A-AAE9-F5AEA6D1D881

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Q50289006-8F3C104D-81F7-4023-B9D0-EB9F70137E88

P3937

Q50289006-BC9B92FE-66DD-414D-B4B6-3BD50A545029

P527

Q50289006-1475DE28-2277-49AC-8225-FB53C57C6F0C

Q50289006-1B21B114-9D5C-44D3-B38B-795E1B342A0D

P703

Q50289006-6DFAB550-1807-4B08-8456-E47B73A592E0

P2860

Somatic mutation of TSSC5, a novel imprinted gene from human chromosome 11p15.5

Transcriptional map of 170-kb region at chromosome 11p15.5: identification and mutational analysis of the BWR1A gene reveals the presence of mutations in tumor samples

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reactome:R-HSA-5625574

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biological process

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Defective SLC22A18 causes lung cancer (LNCR) and embryonal rhabdomyosarcoma 1 (RMSE1)

P3937

R-HSA-5625574

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

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SLC22A18 substrates

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