Variant ID | 22400 |
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Entrez Gene ID | 7547 |
Gene | ZIC3 (GeneCards) |
Location | hg19 X:137156552-137156552
hg38 X:138074393-138074393 |
Disease | Xeroderma Pigmentosum (view all the variants in this disease) |
Method | HiSeq X Ten |
Mutation(HGVS format) | NC_000023.10:g.137156552 A>G (Genome Assembly: GRCh37) |
Exon or Intron | NA |
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Position in protein | NA |
Amino acid changes in protein | NA > NA |
Position in cDNA | NA |
Changes in cDNA | NA > NA |
mRNA accession | NA |
mRNA length | NA |
Reference length | 155270560 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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CADD Raw score (version 1.3) | 0.154834 (Deleterious) |
FATHMM raw prediction score | 0.0774 (Tolerated) |
Deleterious probability by DeFine | 0.0869 (Neutral) |
Entrez Gene ID | 7547 (NCBI Gene) |
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Official Gene Symbol | ZIC3 (GeneCards) |
Number of variants in ZIC3 in this database | 11 (view all the variants) |
Full name | Zic family member 3 |
Band | Xq26.3 |
Other IDs | Vega: OTTHUMG00000022525 OMIM: 300265 HGNC: HGNC:12874 Ensembl: ENSG00000156925 |
Other names | HTX, HTX1, ZNF203, VACTERLX |
Summary | This gene encodes a member of the ZIC family of C2H2-type zinc finger proteins. This nuclear protein probably functions as a transcription factor in early stages of left-right body axis formation. Mutations in this gene cause X-linked visceral heterotaxy, which includes congenital heart disease and left-right axis defects in organs. [provided by RefSeq, Jul 2008] |
Individual ID | 29217584.24 (view all the variants in this individual) |
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Pubmed ID | 29217584 |
Whose mosaic mutation | Female Patient |
Phenotype | 3 |
Disease | Xeroderma Pigmentosum (view all the variants in this disease) |
OMIM ID | 278700 |
Pubmed ID | 29217584 |
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Title | Aging and neurodegeneration are associated with increased mutations in single human neurons. |
Journal | Science |
Publication date | 2018.02 |
Disease | Cockayne syndrome Xeroderma Pigmentosum |
Number of cases | Male cases: 3; Female cases: 6; cases of unknown sex: 15; |