Source: UNIPROT

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 26009
Gene Symbol: ZZZ3
ZZZ3
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.300 GeneticVariation UNIPROT

Entrez Id: 57688
Gene Symbol: ZSWIM6
ZSWIM6
CUI: C1863616
Disease: ACROMELIC FRONTONASAL DYSOSTOSIS
ACROMELIC FRONTONASAL DYSOSTOSIS 		0.740 GeneticVariation UNIPROT Immunohistochemistry of later-stage mouse embryos demonstrated tissue-specific expression in the derivatives of all three germ layers. qRT-PCR expression analysis of osteoblast and fibroblast cell lines available from two probands was suggestive of Hedgehog pathway activation, indicating that the ZSWIM6 mutation associated with AFND may lead to the craniofacial, brain and limb malformations through the disruption of Hedgehog signaling. 25105228

2014
Entrez Id: 79149
Gene Symbol: ZSCAN5A
ZSCAN5A
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.300 GeneticVariation UNIPROT

Entrez Id: 80345
Gene Symbol: ZSCAN16
ZSCAN16
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.300 GeneticVariation UNIPROT

Entrez Id: 7784
Gene Symbol: ZP3
ZP3
CUI: C4540205
Disease: OOCYTE MATURATION DEFECT 3
OOCYTE MATURATION DEFECT 3 		0.600 GeneticVariation UNIPROT A Recurrent Missense Mutation in ZP3 Causes Empty Follicle Syndrome and Female Infertility. 28886344

2017
Entrez Id: 54680
Gene Symbol: ZNHIT6
ZNHIT6
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.300 GeneticVariation UNIPROT

Entrez Id: 9326
Gene Symbol: ZNHIT3
ZNHIT3
CUI: C1850055
Disease: PEHO syndrome
PEHO syndrome 		0.730 GeneticVariation UNIPROT Transfection of cell lines with ZNHIT3 expression vectors showed that the PEHO syndrome mutant protein is unstable. 28335020

2017
Entrez Id: 741
Gene Symbol: ZNHIT2
ZNHIT2
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.300 GeneticVariation UNIPROT

Entrez Id: 10467
Gene Symbol: ZNHIT1
ZNHIT1
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.300 GeneticVariation UNIPROT

Entrez Id: 91752
Gene Symbol: ZNF804A
ZNF804A
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.300 GeneticVariation UNIPROT

Entrez Id: 7627
Gene Symbol: ZNF75A
ZNF75A
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.300 GeneticVariation UNIPROT

Entrez Id: 7552
Gene Symbol: ZNF711
ZNF711
CUI: C2749020
Disease: Mental Retardation, X-Linked, Znf711-Related
Mental Retardation, X-Linked, Znf711-Related 		0.600 GeneticVariation UNIPROT A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation. 19377476

2009
Entrez Id: 7552
Gene Symbol: ZNF711
ZNF711
CUI: C2749020
Disease: Mental Retardation, X-Linked, Znf711-Related
Mental Retardation, X-Linked, Znf711-Related 		0.600 GeneticVariation UNIPROT Mutations in two large pedigrees highlight the role of ZNF711 in X-linked intellectual disability. 27993705

2017
Entrez Id: 57592
Gene Symbol: ZNF687
ZNF687
CUI: C4085250
Disease: PAGET DISEASE OF BONE 6
PAGET DISEASE OF BONE 6 		0.400 GeneticVariation UNIPROT ZNF687 Mutations in Severe Paget Disease of Bone Associated with Giant Cell Tumor. 26849110

2016
Entrez Id: 79759
Gene Symbol: ZNF668
ZNF668
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.310 GeneticVariation UNIPROT

Entrez Id: 9726
Gene Symbol: ZNF646
ZNF646
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.300 GeneticVariation UNIPROT

Entrez Id: 84146
Gene Symbol: ZNF644
ZNF644
CUI: C3279997
Disease: MYOPIA 21, AUTOSOMAL DOMINANT
MYOPIA 21, AUTOSOMAL DOMINANT 		0.600 GeneticVariation UNIPROT Detection of mutations in LRPAP1, CTSH, LEPREL1, ZNF644, SLC39A5, and SCO2 in 298 families with early-onset high myopia by exome sequencing. 25525168

2014
Entrez Id: 84146
Gene Symbol: ZNF644
ZNF644
CUI: C3279997
Disease: MYOPIA 21, AUTOSOMAL DOMINANT
MYOPIA 21, AUTOSOMAL DOMINANT 		0.600 GeneticVariation UNIPROT Study of a US cohort supports the role of ZNF644 and high-grade myopia susceptibility. 22539872

2012
Entrez Id: 84146
Gene Symbol: ZNF644
ZNF644
CUI: C3279997
Disease: MYOPIA 21, AUTOSOMAL DOMINANT
MYOPIA 21, AUTOSOMAL DOMINANT 		0.600 GeneticVariation UNIPROT Exome sequencing identifies ZNF644 mutations in high myopia. 21695231

2011
Entrez Id: 84146
Gene Symbol: ZNF644
ZNF644
CUI: C3279997
Disease: MYOPIA 21, AUTOSOMAL DOMINANT
MYOPIA 21, AUTOSOMAL DOMINANT 		0.600 GeneticVariation UNIPROT New ZNF644 mutations identified in patients with high myopia. 24991186

2014
Entrez Id: 84146
Gene Symbol: ZNF644
ZNF644
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.300 GeneticVariation UNIPROT

Entrez Id: 57547
Gene Symbol: ZNF624
ZNF624
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.300 GeneticVariation UNIPROT

Entrez Id: 137209
Gene Symbol: ZNF572
ZNF572
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.300 GeneticVariation UNIPROT

Entrez Id: 148266
Gene Symbol: ZNF569
ZNF569
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.310 GeneticVariation UNIPROT

Entrez Id: 147741
Gene Symbol: ZNF560
ZNF560
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.300 GeneticVariation UNIPROT