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Human Disease and Mouse Model Detail
Human Disease Spermatogenic Failure, Y-Linked, 2; SPGFY2
OMIM ID: 415000
Synonyms Azoospermia, Nonobstructive, Y-Linked; Oligospermia, Nonobstructive, Y-Linked; Oligozoospermia, Nonobstructive, Y-Linked; Spermatogenic Failure; Spermatogenic Failure, Nonobstructive, Y-Linked
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Gene is associated with the disease in this species
      Mouse Homologs Human Homologs Mouse Models Mouse : Human
Homology Class
     BPY2*  
CDY1*, CDY2A*, CDY1B, CDY2B   0:4 Homology
DAZ1*, DAZ4   0:2 Homology
DAZ3*   0:1 Homology
Dazl DAZ2*   1:1 Homology
Ddx3y DDX3Y*   1:1 Homology
Hsfy2 HSFY1*, HSFY2   1:2 Homology
Kdm5d KDM5D*   1:1 Homology
PRY*  
PRY2*  
RBMY1A1*, RBMY1B, RBMY1D, RBMY1E, RBMY1F, RBMY1J   0:6 Homology
RPS4Y2*   0:1 Homology
Usp9y USP9Y*   1:1 Homology
VCY*, VCX2, VCY1B   0:3 Homology
XKRY*, XKRY2   0:2 Homology

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
11/18/2014
MGI 5.20
The Jackson Laboratory