Variant ID | 26467 |
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Entrez Gene ID | 767558 |
Gene | LUZP6 (GeneCards) |
Location | hg19 7:136219150-136219150
hg38 7:136534402-136534402 |
Disease | Asymptomatic |
Method | Single cell Sequencing Cell cloning |
Mutation(HGVS format) | NC_000007.13:g.136219150 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 | 159138663 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | -0.2789 |
CADD Raw score (version 1.3) | 0.257637 (Deleterious) |
FATHMM raw prediction score | 0.1121 (Tolerated) |
Deleterious probability by DeFine | 0.1617 (Neutral) |
Entrez Gene ID | 767558 (NCBI Gene) |
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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 | 29217587.03 (view all the variants in this individual) |
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Pubmed ID | 29217587 |
Whose mosaic mutation | Normal |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |