Annotation Detail
Information
- Associated Genes
- NPAS2
- Associated Variants
-
NPAS2 MUTATION
NPAS2 MUTATION - Associated Disease
- Azoospermia, Nonobstructive
- Source Database
- DisGeNET
- Description
- Whole-exome sequencing identifies novel homozygous mutation in NPAS2 in family with nonobstructive azoospermia.
- Pubmed
- 25956372
- Section of the abstract supporting the evidence
- TITLE
- Number of the section of the abstract supporting the evidence
- 0
- Number of the sentence supporting the evidence
- 0
- Original source reporting the Gene Disease association
- BeFree
- DisGENET score for the Gene Disease association
- 0.000271441872080303
Drugs