All terms in MeSH

Label Id Description
Loss of Function Mutation D000073658 [A mutation that causes a decrease in or elimination of a gene product's activity. ]
PMM1 protein, human C000629934
Gain of Function Mutation D000073659 [A mutation that results in an increase in a gene's activity or in acquiring a new molecular function or a new pattern of gene expression. ]
PCN-1 protein, C elegans C000629935
Tafa2 protein, mouse C000629936
RPSA protein, Xenopus C000629937
Qrich2 protein, mouse C000629938
LIMD2 protein, human C000629939
Fermium-255 C000615200
Nobelium-254 C000615201
Hydrogen-4 C000615202
juniper berry oil C115013
Hydrogen-5 C000615203
bar-1 protein, C elegans C115014
Hydrogen-6 C000615204
PKC-3 protein C115015
Hydrogen-7 C000615205
polyetherurethane C115016
Helium-3 C000615206
SPT15 protein, S cerevisiae C115017