Variant: rs104894261 

    present in Gene: MAP4K2;MEN1
    present in Chromosome: 11
    Position on Chromosome: 64804588
    Alleles of this Variant: G/A

rs104894261 in MAP4K2;MEN1 gene and Multiple Endocrine Neoplasia Type 1 PMID 17853334 2007 Developing effective screening strategies in multiple endocrine neoplasia type 1 (MEN 1) on the basis of clinical and sequencing data of German patients with MEN 1.

PMID 9103196 1997 Positional cloning of the gene for multiple endocrine neoplasia-type 1.

PMID 24218143 2014 Ectopic Cushing syndrome associated with thymic carcinoid tumor as the first presentation of MEN1 syndrome-report of a family with MEN1 gene mutation.

PMID 11578300 2001 Prospective controlled trial of a standardized meal stimulation test in the detection of pancreaticoduodenal endocrine tumours in patients with multiple endocrine neoplasia type 1.

PMID 16449969 2006 Tumor suppressor menin: the essential role of nuclear localization signal domains in coordinating gene expression.

PMID 15331604 2004 Direct binding of DNA by tumor suppressor menin.

rs104894261 in MAP4K2;MEN1 gene and Neoplastic Syndromes, Hereditary PMID 22470073 2012 Primary hyperparathyroidism in MEN1 patients: a cohort study with longterm follow-up on preferred surgical procedure and the relation with genotype.

PMID 9103196 1997 Positional cloning of the gene for multiple endocrine neoplasia-type 1.