Prdm13 - PR/SET domain 13
Predicted to enable chromatin binding activity. Predicted to be involved in negative regulation of transcription by RNA polymerase II and positive regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. Is expressed in several structures, including central brain primordium; embryonic stomatogastric nervous system; ganglia; stomatogastric nervous system primordium; and ventral nerve cord primordium. Used to study North Carolina macular dystrophy. Human ortholog(s) of this gene implicated in pontocerebellar hypoplasia. Orthologous to human PRDM13 (PR/SET domain 13). [provided by Alliance of Genome Resources, Dec 2024]
NCBI Orthologs
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Protein alignment
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Species | Gene | Architecture | aa |
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