Term:spermatogenic failure 7
go back to main search page
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
For additional species annotation, visit the Alliance of Genome Resources.

show annotations for term's descendants       view all columns           Sort by:
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

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 7 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
                  Asthenozoospermia 8
                    spermatogenic failure 7 3
paths to the root


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