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Immunogen sequence: RVPSKEDDKE IDLEHLHRRV NSLCTDDDSP HKQFSTSSID LTPLDIDTLP TRQALEQISD FRNTHITTTT FIPEQIQTLS RTLSAKAASG FTFGNVPEHR TGPFRHRAPN GGFFRSPIKT MSSIPYQPTP TLGLNLGNDP DR
Highest antigen sequence identity to the following orthologs: Mouse - 99%, Rat - 99%.
GRID2 is a member of the family of ionotropic glutamate receptors which are the predominant excitatory neurotransmitter receptors in the mammalian brain. The encoded protein is a multi-pass membrane protein that is expressed selectively in cerebellar Purkinje cells. A point mutation in the mouse ortholog, associated with the phenotype named 'lurcher', in the heterozygous state leads to ataxia resulting from selective, cell-autonomous apoptosis of cerebellar Purkinje cells during postnatal development. Mice homozygous for this mutation die shortly after birth from massive loss of mid- and hindbrain neurons during late embryogenesis. This protein also plays a role in synapse organization between parallel fibers and Purkinje cells. Alternate splicing results in multiple transcript variants encoding distinct isoforms. Mutations in this gene cause cerebellar ataxia in humans.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: GluD2; gluR delta-2 subunit; glutamate receptor; glutamate receptor delta-2 subunit; Glutamate receptor ionotropic, delta-2; glutamate receptor, ionotropic, delta 2
基因别名: GluD2; GLURD2; GRID2; SCAR18
UniProt ID: (Human) O43424
Entrez Gene ID: (Human) 2895