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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

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     BPY2*   HGNC
CDY1*, CDY2A*, CDY1B, CDY2B   HomoloGene
DAZ1*, DAZ4   HomoloGene
DAZ2*   HGNC
DAZ3*   HomoloGene
DDX3Y* Ddx3y   HomoloGene and HGNC
HSFY1*, HSFY2 Hsfy2   HomoloGene
KDM5D* Kdm5d   HomoloGene and HGNC
PRY*   HGNC
PRY2*   HGNC
RBMY1A1*, RBMY1B, RBMY1D, RBMY1E, RBMY1F, RBMY1J   HomoloGene
RPS4Y2*   HomoloGene
USP9Y* Usp9y   HomoloGene
VCY*, VCX2, VCY1B   HomoloGene
XKRY*, XKRY2   HomoloGene

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
07/28/2015
MGI 5.22
The Jackson Laboratory