Variant ID | 11183 |
---|---|
Entrez Gene ID | 767558 |
Gene | LUZP6 (GeneCards) |
Location | hg19 7:135928055-135928055
hg38 7:136243307-136243307 |
Disease | Asymptomatic |
Method | HiSeq X Ten |
Mutation(HGVS format) | NC_000007.13:g.135928055 T>C (Genome Assembly: GRCh37) |
Exon or Intron | NA |
---|---|
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 | 159138663 |
MAF in gnomAD genome (version 2.0.1) | 0 |
---|---|
EIGEN score | 0.0105 |
CADD Raw score (version 1.3) | 0.06831 (Deleterious) |
FATHMM raw prediction score | 0.15443 (Tolerated) |
Deleterious probability by DeFine | 0.3509 (Neutral) |
Entrez Gene ID | 767558 (NCBI Gene) |
---|---|
Official Gene Symbol | LUZP6 (GeneCards) |
Number of variants in LUZP6 in this database | 12 (view all the variants) |
Full name | leucine zipper protein 6 |
Band | 7q33 |
Other IDs | Vega: OTTHUMG00000180445 OMIM: 611050 HGNC: HGNC:33955 Ensembl: ENSG00000267697 |
Other names | MPD6, MTPNUT |
Summary | A bi-cistronic transcript encodes the products of both the myotrophin and leucine zipper protein 6 genes, which are located on chromosome 7. A cryptic ORF at the 3' end of the myotrophin transcript uses a novel internal ribosome entry site and a non-AUG translation initiation codon to produce leucine zipper protein 6, a 6.4 kDa tumor antigen that is associated with myeloproliferative disease. [provided by RefSeq, Jul 2008] |
Individual ID | 29217584.13 (view all the variants in this individual) |
---|---|
Pubmed ID | 29217584 |
Whose mosaic mutation | Normal |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |
Pubmed ID | 29217584 |
---|---|
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; |