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Term:spermatogenic failure 3
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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
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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

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Path 1
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  disease 14759
    Developmental Diseases 7628
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 6666
        genetic disease 5913
          spermatogenic failure 3 3
Path 2
Term Annotations click to browse term
  disease 14759
    disease of anatomical entity 13978
      Urogenital Diseases 3755
        Female Urogenital Diseases and Pregnancy Complications 1530
          Female Urogenital Diseases 1281
            female reproductive system disease 1277
              infertility 197
                male infertility 138
                  azoospermia 23
                    spermatogenic failure 3 3
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