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Details
Link-It Detail - Human Phenotype - Abnormal spermatogenesis
Debug Stats
  • ### Total Build Time: 40 ms 28.906 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 199 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 218 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=7 ms Completed: 7 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=4 ms Completed: 4 ms rowSize= 811 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 1.043 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=6 ms Completed: 6 ms rowSize= 3.064 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=14 ms Completed: 14 ms rowSize= 22.437 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.019 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormal spermatogenesis HP:0008669
Definition (1)
Incomplete maturation or aberrant formation of the male gametes.
Parents (2)
img Abnormality of male internal genitalia HP:0000022
img Functional abnormality of male internal genitalia HP:0000025
Children (3)
img Globozoospermia HP:0012205
img Azoospermia HP:0000027
img Oligospermia HP:0000798
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of male internal genitalia HP:0000022
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of male internal genitalia HP:0000022
img All HP:0000001img Phenotypic abnormality HP:00001187img Functional abnormality of male internal genitalia HP:0000025
Genes (26)

Species:
human : 26
Page Size
Current 25
  Page 1 of 2
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanMYMY4100653379Moyamoya disease 4
img HP RolledUp, OMIM ID: 300845
HumanSRXX210065337846XX sex reversal 2
img HP RolledUp, OMIM ID: 278850
HumanDEL15Q15.3100240731
img HP TAS, OMIM ID: 611102
HumanDPY19L2283417dpy-19-like 2 (C. elegans)
img HP RolledUp, OMIM ID: 613958
HumanSTRC161497stereocilin
img HP RolledUp, OMIM ID: 612997
HumanCATSPER2117155cation channel, sperm associated 2
img HP RolledUp, OMIM ID: 612997
HumanCATSPER1117144cation channel, sperm associated 1
img HP RolledUp, OMIM ID: 612997
HumanSLC29A355315solute carrier family 29 (equilibrative nucleoside transporter), member 3
img HP RolledUp, OMIM ID: 612391
HumanSYCP350511synaptonemal complex protein 3
img HP RolledUp, OMIM ID: 270960
HumanPOC1A25886POC1 centriolar protein A
img HP RolledUp, OMIM ID: 614813
HumanSEMA3A10371sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A
img HP RolledUp, OMIM ID: 614897
HumanUSP9Y8287ubiquitin specific peptidase 9, Y-linked
img HP RolledUp, OMIM ID: 415000
HumanCNBP7555CCHC-type zinc finger, nucleic acid binding protein
img HP RolledUp, OMIM ID: 602668
HumanTKCR7085torticollis, keloids, cryptorchidism and renal dysplasia
img HP RolledUp, OMIM ID: 314300
HumanSCP26342sterol carrier protein 2
img HP RolledUp, OMIM ID: 613724
HumanRBMY1A15940RNA binding motif protein, Y-linked, family 1, member A1
img HP RolledUp, OMIM ID: 415000
HumanHFE3077hemochromatosis
img HP RolledUp, OMIM ID: 235200
HumanNR5A12516nuclear receptor subfamily 5, group A, member 1
img HP RolledUp, OMIM ID: 613957
HumanF13A12162coagulation factor XIII, A1 polypeptide
img HP RolledUp, OMIM ID: 134570
HumanDAZ11617deleted in azoospermia 1
img HP RolledUp, OMIM ID: 400003
HumanCFTR1080cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
img HP RolledUp, OMIM ID: 277180
HumanBMP2650bone morphogenetic protein 2
img HP RolledUp, OMIM ID: 235200
HumanBLM641Bloom syndrome, RecQ helicase-like
img HP RolledUp, OMIM ID: 210900
HumanAZF1560azoospermia factor 1
img HP RolledUp, OMIM ID: 415000
HumanATM472ataxia telangiectasia mutated
img HP IEA, OMIM ID: 208900
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0008669Abnormal spermatogenesis0self