Symbol Name ID |
Sms
spermine synthase MGI:109490 |
Darker colors indicate more annotations |
Human Phenotypes | Hypospadias |
Abnormality of the Leydig cells |
Cryptorchidism |
Testicular atrophy |
Disease(s) Associated with SMS | ||||
syndromic X-linked intellectual disability Snyder type |
Mouse Phenotypes | oligozoospermia |
testis degeneration |
abnormal fertility/fecundity |
male infertility |
reduced male fertility |
|
Availability | Mouse Genotype | |||||
Smstm1a(EUCOMM)Wtsi/Smstm1a(EUCOMM)Wtsi | ||||||
Smstm1a(EUCOMM)Wtsi/Y |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 08/02/2024 MGI 6.24 |
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