Term:spermatogenic failure 3
go back to main search page
Accession:DOID:0070168 term browser browse the term
Definition:A male infertility characterized by autosomal dominant inheritance of nonobstructive asthenozoospermia that has_material_basis_in heterozygous mutation in the SLC26A8 gene on chromosome 6p21. (DO)
Synonyms:exact_synonym: NON-OBSTRUCTIVE AZOOSPERMIA;   SPGF3;   nonobstructive azoospermia
 primary_id: MESH:C564665
 alt_id: DOID:9005015;   OMIM:606766;   RDO:0013547
For additional species annotation, visit the Alliance of Genome Resources.

show annotations for term's descendants       view all columns           Sort by:
spermatogenic failure 3 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Npas2 neuronal PAS domain protein 2 JBrowse link 9 45,901,262 46,081,880 RGD:8554872
G Slc26a8 solute carrier family 26 member 8 JBrowse link 20 5,870,714 5,933,151 RGD:7240710
G Srsf6 serine and arginine rich splicing factor 6 JBrowse link 3 159,305,345 159,310,668 RGD:11039404

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14926
    Developmental Diseases 7774
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7096
        genetic disease 6457
          spermatogenic failure 3 3
Path 2
Term Annotations click to browse term
  disease 14926
    disease of anatomical entity 14092
      Urogenital Diseases 3915
        Female Urogenital Diseases and Pregnancy Complications 1687
          Female Urogenital Diseases 1436
            female reproductive system disease 1432
              infertility 203
                male infertility 144
                  azoospermia 24
                    spermatogenic failure 3 3
paths to the root


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.