PRDM8


Summary: This gene encodes a protein that belongs to a conserved family of histone methyltransferases that predominantly act as negative regulators of transcription. The encoded protein contains an N-terminal Su(var)3-9, Enhancer-of-zeste, and Trithorax (SET) domain and a double zinc-finger domain. Knockout of this gene in mouse results in mistargeting by neurons of the dorsal telencephalon, abnormal itch-like behavior, and impaired differentiation of rod bipolar cells. In humans, the protein has been shown to interact with the phosphatase laforin and the ubiquitin ligase malin, which regulate glycogen construction in the cytoplasm. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016].

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Name
OMIM ID
Ensembl ID
HGNC ID
PHARMGKB ID
Map Location
OMIM IDMIM:616639
PHARMGKB IDPA33720
Map Location4q21.21

Gene Categories:

METHYL TRANSFERASE

GO terms in PRDM8


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Term Type
Evidence Type
GO Term ID
GO Des.
BP IEA GO:0006351 transcription, DNA-templated
BP IEA GO:0006357 regulation of transcription by RNA polymerase II
BP IBA GO:0014003 oligodendrocyte development
BP IEA GO:0032259 methylation
CC IDA GO:0005634 nucleus
MF ISA GO:0000981 RNA polymerase II transcription factor activity, sequence-specific DNA binding
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Gene expression in normal tissue: PRDM8

Gene-model tissue-cancer distribution: Bubble Plot

Gene-drug pathway distribution

Pathways in PRDM8


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Database
Pathway ID
Pathway Des.
No matching records found

Gene-Drug: Aster Plot


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Drug ID
Drug Name
Model Num.
iGMDRD353 PD0325901 1
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Gene in drug-gene network: Network Plot

Gene-drug targets distribution

Gene Structure: PDB

Models in PRDM8

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Model
Level
Reference ID
Tissue
Cancer
Drug
Clinical Response
Source
No matching records found

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