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Term:spermatogenic failure 7
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Accession:DOID:0070173 term browser browse the term
Definition:A male infertility characterized by autosomal recessive inheritance of impaired or absent sperm motility and increased incidence of morphologically abnormal sperm that has_material_basis_in mutation in the CATSPER1 gene on chromosome 11q13. (DO)
Synonyms:exact_synonym: MIAR;   Male Infertility, Nonsyndromic, Autosomal Recessive;   SPGF7
 primary_id: MESH:C567832
 alt_id: DOID:9000594;   OMIM:612997;   RDO:0012055
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spermatogenic failure 7 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Catsper1 cation channel, sperm associated 1 JBrowse link 1 220,715,000 220,724,235 RGD:7240710
G Catsper2 cation channel, sperm associated 2 JBrowse link 3 113,357,361 113,379,498 RGD:11554173
G Strc stereocilin JBrowse link 3 113,324,403 113,343,513 RGD:11554173

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  disease 14759
    Developmental Diseases 7628
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 6666
        genetic disease 5913
          spermatogenic failure 7 3
Path 2
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  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
                  Asthenozoospermia 8
                    spermatogenic failure 7 3
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