Variant ID | 10016 |
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Entrez Gene ID | 8521 |
Gene | GCM1 (GeneCards) |
Location | hg19 6:53102075-53102075
hg38 6:53237277-53237277 |
Disease | Asymptomatic |
Method | HiSeq X Ten |
Mutation(HGVS format) | NC_000006.11:g.53102075 C>T (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 | 171115067 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | -0.1042 |
CADD Raw score (version 1.3) | 0.271679 (Deleterious) |
FATHMM raw prediction score | 0.13333 (Tolerated) |
Deleterious probability by DeFine | 0.4161 (Neutral) |
Entrez Gene ID | 8521 (NCBI Gene) |
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Official Gene Symbol | GCM1 (GeneCards) |
Number of variants in GCM1 in this database | 4 (view all the variants) |
Full name | glial cells missing homolog 1 |
Band | 6p12.1 |
Other IDs | Vega: OTTHUMG00000014871 OMIM: 603715 HGNC: HGNC:4197 Ensembl: ENSG00000137270 |
Other names | GCMA, hGCMa |
Summary | This gene encodes a DNA-binding protein with a gcm-motif (glial cell missing motif). The encoded protein is a homolog of the Drosophila glial cells missing gene (gcm). This protein binds to the GCM-motif (A/G)CCCGCAT, a novel sequence among known targets of DNA-binding proteins. The N-terminal DNA-binding domain confers the unique DNA-binding activity of this protein. [provided by RefSeq, Jul 2008] |
Individual ID | 29217584.15 (view all the variants in this individual) |
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Pubmed ID | 29217584 |
Whose mosaic mutation | Normal |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |
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; |