| Name |
|---|
PTCPRN GenePapillary thyroid carcinoma with papillary renal neoplasia |
MEN1 Genemultiple endocrine neoplasia I This gene encodes menin, a tumor suppressor associated with a syndrome known as multiple endocrine neoplasia type 1. Menin is a scaffold protein that functions in histone modification and epigenetic gene regulation. It is thought to regulate several pathways and processes by altering chromatin structure through the modification of histones. [provided by RefSeq, May 2019] |
CLLS2 GeneDisrupted in B-cell neoplasia |
CNC2 GeneCarney complex type 2, multiple neoplasia and lentiginosis |
CRNDE Genecolorectal neoplasia differentially expressed (non-protein coding) This gene is transcribed into multiple transcript variants, some of which may function as non-coding RNAs. One of the transcript variants encodes a putative short protein that is localized to the nucleus (PMID:25978564). Expression of this locus is increased in proliferating tissues, including certain tumors such as colorectal adenomas and adenocarcinomas. Transcription from this gene is negatively regulated by insulin and insulin-like growth factors, and may regulate the expression of genes involved in metabolism. [provided by RefSeq, May 2015] |