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Symbol
Name
ID
Chromosome
Cyp17a1
cytochrome P450, family 17, subfamily a, polypeptide 1
MGI:88586
19
14 mapping experiments
Experiment Type Details Chromosome Reference
CROSS Cross Type: Backcross
19 J:56826 Herron BJ, et al., Scraggly, a new hair loss mutation on mouse chromosome 19. Mamm Genome. 1999 Sep;10(9):864-9
CROSS Cross Type: Backcross
19 J:56826 Herron BJ, et al., Scraggly, a new hair loss mutation on mouse chromosome 19. Mamm Genome. 1999 Sep;10(9):864-9
CROSS Cross Type: Backcross
19 J:20807 Keller SA, et al., Kidney and retinal defects (Krd), a transgene-induced mutation with a deletion of mouse chromosome 19 that includes the Pax2 locus. Genomics. 1994 Sep 15;23(2):309-20
CROSS Cross Type: Backcross
19 J:20807 Keller SA, et al., Kidney and retinal defects (Krd), a transgene-induced mutation with a deletion of mouse chromosome 19 that includes the Pax2 locus. Genomics. 1994 Sep 15;23(2):309-20
CROSS Cross Type: Backcross
19 J:18648 O'Brien EP, et al., Molecular map of chromosome 19 including three genes affecting bleeding time: ep, ru, and bm. Mamm Genome. 1994 Jun;5(6):356-60
CROSS Cross Type: Intercross
19 J:68175 Rieger DK, et al., A double-deletion mutation in the pitx3 gene causes arrested lens development in aphakia mice. Genomics. 2001 Feb 15;72(1):61-72
CROSS Cross Type: Backcross
19 J:11237 Youngblood GL, et al., Isolation, characterization, and chromosomal mapping of mouse P450 17 alpha-hydroxylase/C17-20 lyase. Genomics. 1991 May;10(1):270-5
CROSS Cross Type: Backcross
19 J:11237 Youngblood GL, et al., Isolation, characterization, and chromosomal mapping of mouse P450 17 alpha-hydroxylase/C17-20 lyase. Genomics. 1991 May;10(1):270-5
TEXT-Genetic Cross 19 J:42484 Gardner JM, et al., The mouse pale ear (ep) mutation is the homologue of human Hermansky-Pudlak syndrome. Proc Natl Acad Sci U S A. 1997 Aug 19;94(17):9238-43
TEXT-Genetic Cross 19 J:56826 Herron BJ, et al., Scraggly, a new hair loss mutation on mouse chromosome 19. Mamm Genome. 1999 Sep;10(9):864-9
TEXT-Genetic Cross 19 J:20828 Taylor BA, et al., The retinal outer segment membrane protein-1 gene (Rom1) maps to the proximal end of mouse chromosome 19. Genomics. 1994 Sep 15;23(2):510-1
TEXT-Physical Mapping 19 J:68175 Rieger DK, et al., A double-deletion mutation in the pitx3 gene causes arrested lens development in aphakia mice. Genomics. 2001 Feb 15;72(1):61-72
TEXT-QTL 19 J:91457 Buck KJ, et al., Mapping murine loci for physical dependence on ethanol. Psychopharmacology (Berl). 2002 Apr;160(4):398-407
TEXT-Radiation Hybrid 19 J:68900 The Jackson Laboratory Mouse Radiation Hybrid Database, Mouse T31 Radiation Hybrid Data Load. Database Release. 2004;

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