Human Disease and Mouse Model Detail
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Human Disease
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Spermatogenic Failure, Y-Linked, 2; SPGFY2
OMIM ID: 415000
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Synonyms
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Azoospermia, Nonobstructive, Y-Linked;
Oligospermia, Nonobstructive, Y-Linked;
Oligozoospermia, Nonobstructive, Y-Linked;
Spermatogenic Failure, Nonobstructive, Y-Linked
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Genes and
mouse models
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Mutations in human and/or mouse homologs are associated with this disease
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*Gene is associated with the disease in this species |
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BPY2*
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CDY1*,
CDY2A*,
CDY1B,
CDY2B
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0:4 Homology
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D1Pas1
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DDX3Y*
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1:1 Homology
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DAZ1*,
DAZ4
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0:2 Homology
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DAZ3*
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0:1 Homology
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Dazl
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DAZ2*
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1:1 Homology
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Hsfy2
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HSFY1*,
HSFY2
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1:2 Homology
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Kdm5d
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KDM5D*
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1:1 Homology
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PRY*
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PRY2*
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RBMY1A1*,
RBMY1B,
RBMY1D,
RBMY1E,
RBMY1F,
RBMY1J
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0:6 Homology
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RPS4Y2*
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0:1 Homology
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Usp9y
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USP9Y*
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1:1 Homology
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VCY*,
VCY1B
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0:2 Homology
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XKRY*,
XKRY2
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0:2 Homology
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Analysis Tools