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A cDNA open reading frame encoding a dominant-negative mutant NR1 subunit of the NMDA receptor with an asparagine-to-arginine substitution at amino acid 616 (N616R), a hemagglutinin (HA) epitope tag 27 aa from the N terminus and a polyadenylation signal, followed by a loxP-flanked SV40-neo cassette, has replaced the first ~130 base pairs of the endogenous Drd1a gene. (J:121750)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
Phenotypes
Legend：
hm: homozygous
ht: heterozygous
cn: conditional genotype
cx: complex: > 1 genome feature
tg: involves transgenes
ot: other: hemizygous, indeterminate,...
(F): Female
(M): Male
phenotype observed
N: normal phenotype
(#): related diseases count
Phenotypes：
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| Phenotypes |
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References Literature
Title
PMID
Journal
Year
IF
