Source: CURATED

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6885
Gene Symbol: MAP3K7
MAP3K7
CUI: C2931461
Disease: Forney Robinson Pascoe syndrome
Forney Robinson Pascoe syndrome 		0.710 Biomarker GENOMICS_ENGLAND Mutations in MAP3K7 that Alter the Activity of the TAK1 Signaling Complex Cause Frontometaphyseal Dysplasia. 27426733

2016
Entrez Id: 6885
Gene Symbol: MAP3K7
MAP3K7
CUI: C2931461
Disease: Forney Robinson Pascoe syndrome
Forney Robinson Pascoe syndrome 		0.710 GermlineCausalMutation ORPHANET Heterozygous Mutations in MAP3K7, Encoding TGF-β-Activated Kinase 1, Cause Cardiospondylocarpofacial Syndrome. 27426734

2016
Entrez Id: 6885
Gene Symbol: MAP3K7
MAP3K7
CUI: C2931461
Disease: Forney Robinson Pascoe syndrome
Forney Robinson Pascoe syndrome 		0.710 GeneticVariation UNIPROT Heterozygous Mutations in MAP3K7, Encoding TGF-β-Activated Kinase 1, Cause Cardiospondylocarpofacial Syndrome. 27426734

2016
Entrez Id: 6885
Gene Symbol: MAP3K7
MAP3K7
CUI: C2931461
Disease: Forney Robinson Pascoe syndrome
Forney Robinson Pascoe syndrome 		0.710 Biomarker CTD_human

Entrez Id: 6885
Gene Symbol: MAP3K7
MAP3K7
CUI: C4310697
Disease: FRONTOMETAPHYSEAL DYSPLASIA 2
FRONTOMETAPHYSEAL DYSPLASIA 2 		0.610 Biomarker GENOMICS_ENGLAND Which genes to assess in the NGS diagnostics of intellectual disability? The case for a consensus database-driven and expert-curated approach. 30914295

2019
Entrez Id: 6885
Gene Symbol: MAP3K7
MAP3K7
CUI: C0265293
Disease: Frontometaphyseal dysplasia
Frontometaphyseal dysplasia 		0.610 GermlineCausalMutation ORPHANET Mutations in MAP3K7 that Alter the Activity of the TAK1 Signaling Complex Cause Frontometaphyseal Dysplasia. 27426733

2016
Entrez Id: 6885
Gene Symbol: MAP3K7
MAP3K7
CUI: C4310697
Disease: FRONTOMETAPHYSEAL DYSPLASIA 2
FRONTOMETAPHYSEAL DYSPLASIA 2 		0.610 GeneticVariation UNIPROT Mutations in MAP3K7 that Alter the Activity of the TAK1 Signaling Complex Cause Frontometaphyseal Dysplasia. 27426733

2016
Entrez Id: 6885
Gene Symbol: MAP3K7
MAP3K7
CUI: C4310697
Disease: FRONTOMETAPHYSEAL DYSPLASIA 2
FRONTOMETAPHYSEAL DYSPLASIA 2 		0.610 Biomarker GENOMICS_ENGLAND Mutations in MAP3K7 that Alter the Activity of the TAK1 Signaling Complex Cause Frontometaphyseal Dysplasia. 27426733

2016
Entrez Id: 6885
Gene Symbol: MAP3K7
MAP3K7
CUI: C4310697
Disease: FRONTOMETAPHYSEAL DYSPLASIA 2
FRONTOMETAPHYSEAL DYSPLASIA 2 		0.610 Biomarker GENOMICS_ENGLAND Frontometaphyseal dysplasia and keloid formation without FLNA mutations. 25899317

2015
Entrez Id: 6885
Gene Symbol: MAP3K7
MAP3K7
CUI: C0265293
Disease: Frontometaphyseal dysplasia
Frontometaphyseal dysplasia 		0.610 Biomarker CTD_human

Entrez Id: 6885
Gene Symbol: MAP3K7
MAP3K7
CUI: C0265293
Disease: Frontometaphyseal dysplasia
Frontometaphyseal dysplasia 		0.610 Biomarker GENOMICS_ENGLAND

Entrez Id: 6885
Gene Symbol: MAP3K7
MAP3K7
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.330 Biomarker CTD_human Global analysis of differentially expressed genes in androgen-independent prostate cancer. 17199135

2007
Entrez Id: 6885
Gene Symbol: MAP3K7
MAP3K7
CUI: C0005398
Disease: Cholestasis, Extrahepatic
Cholestasis, Extrahepatic 		0.300 Biomarker CTD_human Hepatoprotective activities of rosmarinic acid against extrahepatic cholestasis in rats. 28789951

2017
Entrez Id: 6885
Gene Symbol: MAP3K7
MAP3K7
CUI: C4281559
Disease: FRONTOMETAPHYSEAL DYSPLASIA 1
FRONTOMETAPHYSEAL DYSPLASIA 1 		0.300 Biomarker GENOMICS_ENGLAND These findings show that dysregulation of the TAK1 complex produces a close phenocopy of FMD caused by FLNA mutations. 27426733

2016
Entrez Id: 6885
Gene Symbol: MAP3K7
MAP3K7
CUI: C0033578
Disease: Prostatic Neoplasms
Prostatic Neoplasms 		0.300 Biomarker CTD_human Global analysis of differentially expressed genes in androgen-independent prostate cancer. 17199135

2007