DisGeNET - a database of gene-disease associations

SLC22A18, solute carrier family 22 member 18, 5002

N. diseases: 76; N. variants: 5

Disease: Mammary Neoplasms ×

Source: ALL

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Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _g

DPI _g

pLI

EI _gda

EL _gda

Score _gda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Disease

Score _gda

Association Type

Type

Original DB

Sentence supporting the association

PMID

PMID Year

CUI:	C1458155
Disease:	Mammary Neoplasms

Mammary Neoplasms

0.320

AlteredExpression

group

BEFREE

SPECIMENS AND METHODS: Immunohistochemistry was used to examine SLC22A18 protein expression in the breast tumors.

21144813

2011

CUI:	C1458155
Disease:	Mammary Neoplasms

Mammary Neoplasms

0.320

GeneticVariation

group

LHGDN

Gain of imprinting of SLC22A18 sense and antisense transcripts in human breast cancer.

16624517

2006

CUI:	C1458155
Disease:	Mammary Neoplasms

Mammary Neoplasms

0.320

Biomarker

group

CTD_human