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Symbol
Name
ID
Chromosome
hph1
hyperphenylalaninemia 1
MGI:96214
14
6 mapping experiments
Experiment Type Details Chromosome Reference
CROSS Cross Type: Backcross
14 J:9146 Bode VC, et al., hph-1: a mouse mutant with hereditary hyperphenylalaninemia induced by ethylnitrosourea mutagenesis. Genetics. 1988 Feb;118(2):299-305
CROSS Cross Type: Backcross
14 J:9146 Bode VC, et al., hph-1: a mouse mutant with hereditary hyperphenylalaninemia induced by ethylnitrosourea mutagenesis. Genetics. 1988 Feb;118(2):299-305
CROSS Cross Type: Backcross
14 J:59496 Montanez CS, et al., Linkage analysis of the hph-1 mutation and the GTP cyclohydrolase I structural gene. Mol Genet Metab. 1999 Sep;68(1):91-2
TEXT 14 J:91166 Khoo JP, et al., Congenic mapping and genotyping of the tetrahydrobiopterin-deficient hph-1 mouse. Mol Genet Metab. 2004 Jul;82(3):251-4
TEXT-Genetic Cross 14 J:14082 Bode VC, et al., Hph-1 closely linked to Np-1 on Chromosome 14. Mouse News Lett. 1986;74:97
TEXT-QTL 14 J:58047 Rasmussen E, et al., Identification of quantitative trait loci for haloperidol-induced catalepsy on mouse chromosome 14. J Pharmacol Exp Ther. 1999 Sep;290(3):1337-46

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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory