ERCC6 Chromosome 10

ERCC excision repair 6, chromatin remodeling factor
413 variants 413 Health Risk

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What This Gene Does
This gene encodes a DNA-binding protein that is important in transcription-coupled excision repair. The encoded protein has ATP-stimulated ATPase activity, interacts with several transcription and excision repair proteins, and may promote complex formation at DNA repair sites. Mutations in this gene are associated with Cockayne syndrome type B and cerebrooculofacioskeletal syndrome 1. Alternative splicing occurs between a splice site from exon 5 of this gene to the 3' splice site upstream of the open reading frame (ORF) of the adjacent gene, piggyback-derived-3 (GeneID:267004), which activates the alternative polyadenylation site downstream of the piggyback-derived-3 ORF. The resulting transcripts encode a fusion protein that shares sequence with the product of each individual gene. [provided by RefSeq, Mar 2016]
Gene Info
Gene Group
"SNF2 related family|ERCC excision repair associated|B-WICH chromatin-remodelling complex subunits"
Locus Type
gene with protein product
Location
10q11.23
Ensembl
ENSG00000225830
Associated Conditions (28)
Cockayne syndrome
Cerebrooculofacioskeletal syndrome 1
ERCC6-related disorder
Age related macular degeneration 5
Cockayne syndrome type 2
Inborn genetic diseases
Thymoma
DE SANCTIS-CACCHIONE SYNDROME
Hereditary breast ovarian cancer syndrome
7 conditions
Cone-rod dystrophy
Intellectual disability
6 conditions
Clear cell carcinoma of kidney
Uveal melanoma
Colon adenocarcinoma
Melanoma
Malignant tumor of esophagus
Familial cancer of breast
Ovarian serous cystadenocarcinoma
+8 more conditions
Key Variants
RS1057518910
Conflicting classifications of pathogenicity
Cockayne syndrome, Cerebrooculofacioskeletal syndrome 1, Cockayne syndrome
Health Risk
RS114234514
Conflicting classifications of pathogenicity
ERCC6-related disorder, ERCC6-related disorder
Health Risk
RS114403790
Conflicting classifications of pathogenicity
Cerebrooculofacioskeletal syndrome 1, Age related macular degeneration 5, Cockayne syndrome type 2
Health Risk
RS114490473
Conflicting classifications of pathogenicity
Age related macular degeneration 5, Cerebrooculofacioskeletal syndrome 1, Cockayne syndrome type 2
Health Risk
RS114832108
Conflicting classifications of pathogenicity
Health Risk
RS115633798
Conflicting classifications of pathogenicity
Inborn genetic diseases, Thymoma, Inborn genetic diseases
Health Risk
RS115643329
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS115875661
Conflicting classifications of pathogenicity
Health Risk
RS115876786
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS116032070
Conflicting classifications of pathogenicity
Age related macular degeneration 5, Cerebrooculofacioskeletal syndrome 1, Cockayne syndrome type 2
Health Risk
RS1163269726
Conflicting classifications of pathogenicity
Inborn genetic diseases, Cockayne syndrome type 2, Inborn genetic diseases
Health Risk
RS117555054
Conflicting classifications of pathogenicity
Age related macular degeneration 5, Cerebrooculofacioskeletal syndrome 1, Cockayne syndrome type 2
Health Risk
All Variants (413)
RSID Category Clinical Significance Conditions
RS192242583 Health Risk Conflicting classifications of pathogenicity Age related macular degeneration 5, Cerebrooculofacioskeletal syndrome 1, Cockayne syndrome type 2
RS200079929 Health Risk Conflicting classifications of pathogenicity Age related macular degeneration 5, Cockayne syndrome type 2, Cerebrooculofacioskeletal syndrome 1
RS200093886 Health Risk Conflicting classifications of pathogenicity Cockayne syndrome type 2, Cerebrooculofacioskeletal syndrome 1, Age related macular degeneration 5
RS200431100 Health Risk Conflicting classifications of pathogenicity 7 conditions, 7 conditions
RS201813523 Health Risk Conflicting classifications of pathogenicity Cerebrooculofacioskeletal syndrome 1, Age related macular degeneration 5, Cockayne syndrome type 2
RS201930958 Health Risk Conflicting classifications of pathogenicity Age related macular degeneration 5, Cerebrooculofacioskeletal syndrome 1, Cockayne syndrome type 2
RS367965088 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS369437807 Health Risk Conflicting classifications of pathogenicity Cockayne syndrome type 2, Age related macular degeneration 5, Cerebrooculofacioskeletal syndrome 1
RS370757757 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS371100244 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, 7 conditions, Inborn genetic diseases
RS373277796 Health Risk Conflicting classifications of pathogenicity Cockayne syndrome type 2, 7 conditions, Inborn genetic diseases
RS373710355 Health Risk Conflicting classifications of pathogenicity Cockayne syndrome type 2, Cerebrooculofacioskeletal syndrome 1, Age related macular degeneration 5
RS374791168 Health Risk Conflicting classifications of pathogenicity Cerebrooculofacioskeletal syndrome 1, Cockayne syndrome type 2, Age related macular degeneration 5
RS375175948 Health Risk Conflicting classifications of pathogenicity
RS375181157 Health Risk Conflicting classifications of pathogenicity Cerebrooculofacioskeletal syndrome 1, Cockayne syndrome type 2, Age related macular degeneration 5
RS375617750 Health Risk Conflicting classifications of pathogenicity Cerebrooculofacioskeletal syndrome 1, Age related macular degeneration 5, Cockayne syndrome type 2
RS375921453 Health Risk Conflicting classifications of pathogenicity
RS377708438 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS41562713 Health Risk Conflicting classifications of pathogenicity Cerebrooculofacioskeletal syndrome 1, Age related macular degeneration 5, Cockayne syndrome type 2
RS4253006 Health Risk Conflicting classifications of pathogenicity Age related macular degeneration 5, Cerebrooculofacioskeletal syndrome 1, Cockayne syndrome type 2
RS4253012 Health Risk Conflicting classifications of pathogenicity
RS4253046 Health Risk Conflicting classifications of pathogenicity Cerebrooculofacioskeletal syndrome 1, Cockayne syndrome type 2, Age related macular degeneration 5
RS4253208 Health Risk Conflicting classifications of pathogenicity Cockayne syndrome type 2, Cerebrooculofacioskeletal syndrome 1, Age related macular degeneration 5
RS4253228 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS534095433 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS535616736 Health Risk Conflicting classifications of pathogenicity Age related macular degeneration 5, Cerebrooculofacioskeletal syndrome 1, Cockayne syndrome type 2
RS544471829 Health Risk Conflicting classifications of pathogenicity Cockayne syndrome type 2, Cerebrooculofacioskeletal syndrome 1, Age related macular degeneration 5
RS546407915 Health Risk Conflicting classifications of pathogenicity
RS548033657 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS55698015 Health Risk Conflicting classifications of pathogenicity ERCC6-related disorder, ERCC6-related disorder
RS56089364 Health Risk Conflicting classifications of pathogenicity ERCC6-related disorder, ERCC6-related disorder
RS563142074 Health Risk Conflicting classifications of pathogenicity Cerebrooculofacioskeletal syndrome 1, Cockayne syndrome type 2, Age related macular degeneration 5
RS563356062 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS569564278 Health Risk Conflicting classifications of pathogenicity Cerebrooculofacioskeletal syndrome 1, Age related macular degeneration 5, Cockayne syndrome type 2
RS574272317 Health Risk Conflicting classifications of pathogenicity 7 conditions, 7 conditions
RS61749175 Health Risk Conflicting classifications of pathogenicity Cockayne syndrome type 2, Age related macular degeneration 5, Cerebrooculofacioskeletal syndrome 1
RS61760163 Health Risk Conflicting classifications of pathogenicity 7 conditions, Inborn genetic diseases, Cone-rod dystrophy
RS61760166 Health Risk Conflicting classifications of pathogenicity Cerebrooculofacioskeletal syndrome 1, Cockayne syndrome type 2, Age related macular degeneration 5
RS61760167 Health Risk Conflicting classifications of pathogenicity Cockayne syndrome type 2, Cerebrooculofacioskeletal syndrome 1, Age related macular degeneration 5
RS746330518 Health Risk Conflicting classifications of pathogenicity Cerebrooculofacioskeletal syndrome 1, Cerebrooculofacioskeletal syndrome 1
RS746372685 Health Risk Conflicting classifications of pathogenicity
RS747204355 Health Risk Conflicting classifications of pathogenicity
RS747581337 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS751115103 Health Risk Conflicting classifications of pathogenicity Cerebrooculofacioskeletal syndrome 1, Cockayne syndrome type 2, Age related macular degeneration 5
RS751292948 Health Risk Conflicting classifications of pathogenicity Cockayne syndrome type 2, Inborn genetic diseases, Cockayne syndrome type 2
RS752712823 Health Risk Conflicting classifications of pathogenicity Cerebrooculofacioskeletal syndrome 1, DE SANCTIS-CACCHIONE SYNDROME, Cockayne syndrome type 2
RS756713165 Health Risk Conflicting classifications of pathogenicity 7 conditions, 7 conditions
RS759447711 Health Risk Conflicting classifications of pathogenicity
RS760919459 Health Risk Conflicting classifications of pathogenicity
RS762128995 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
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