DisGeNET - a database of gene-disease associations

SLC39A14, solute carrier family 39 member 14, 23516

N. diseases: 78; N. variants: 10

Disease: Hyperostosis Cranialis Interna ×

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:	C1840404
Disease:	Hyperostosis Cranialis Interna

Hyperostosis Cranialis Interna

0.400

Biomarker

phenotype

HPO

CUI:	C1840404
Disease:	Hyperostosis Cranialis Interna

Hyperostosis Cranialis Interna

0.400

GeneticVariation

phenotype

UNIPROT

Conditional mouse models support the role of SLC39A14 (ZIP14) in Hyperostosis Cranialis Interna and in bone homeostasis.

29621230

2018