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Spermatogenic Failure 8 (SPGF8)

Alias:
Spgf8
Spermatogenic Failure, Type 8
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Spermatogenic Failure 8, also known as spgf8, is related to 46,xy partial gonadal dysgenesis and 45,x/46,xy mixed gonadal dysgenesis. An important gene associated with Spermatogenic Failure 8 is NR5A1 (Nuclear Receptor Subfamily 5 Group A Member 1), and among its related pathways/superpathways is Mammalian disorder of sexual development. Affiliated tissues include testis, and related phenotypes are azoospermia and oligozoospermia
Related ID：
MALACARDS：SPR042
OMIM：613957
MESH：D007248

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
--
14
90
2
SPR042

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Gene
Function
Score
Mutations
No data available

Related Drugs

Name
CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
Journal
Year
IF
No Data Found!
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