prdm16 Gene Set

Dataset GeneRIF Biological Term Annotations
Category structural or functional annotations
Type biological term
Description PR domain containing 16|The reciprocal translocation t(1;3)(p36;q21) occurs in a subset of myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML). This gene is located near the 1p36.3 breakpoint and has been shown to be specifically expressed in the t(1:3)(p36,q21)-positive MDS/AML. The protein encoded by this gene is a zinc finger transcription factor and contains an N-terminal PR domain. The translocation results in the overexpression of a truncated version of this protein that lacks the PR domain, which may play an important role in the pathogenesis of MDS and AML. Alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq, Jul 2008] (NCBI Entrez Gene Database, 63976)
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Genes

8 genes co-occuring with the biological term prdm16 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Symbol Name
LRP1 low density lipoprotein receptor-related protein 1
MECOM MDS1 and EVI1 complex locus
PPARGC1A peroxisome proliferator-activated receptor gamma, coactivator 1 alpha
PRDM16 PR domain containing 16
PRDM2 PR domain containing 2, with ZNF domain
PRDM5 PR domain containing 5
RUNX1 runt-related transcription factor 1
TRPM8 transient receptor potential cation channel, subfamily M, member 8