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Details
Link-It Detail - Jax Mouse Phenotype - abnormal sperm mitochondrial sheath morphology
Debug Stats
  • ### Total Build Time: 101 ms 18.070 KB
  • CONCEPT_NAME gt=4 ms Completed: 4 ms rowSize= 420 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 307 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=1 ms Completed: 1 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=17 ms Completed: 17 ms rowSize= 589 bytes
  • CONCEPT_CHILDREN gt=11 ms Completed: 11 ms rowSize= 590 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=10 ms Completed: 10 ms rowSize= 2.937 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=52 ms Completed: 52 ms rowSize= 11.944 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.184 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal sperm mitochondrial sheath morphology MP:0009832
Definition (1)
any structural anomaly or impairment of the tightly packed helical sheath of ATP-producing mitochondria restricted to the midpiece of the sperm flagellum
Parents (1)
img abnormal sperm midpiece morphology MP:0009831
Children (1)
img absent sperm mitochondrial sheath MP:0009833
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img reproductive system phenotype MP:00053899img abnormal sperm midpiece morphology MP:0009831
img mammalian phenotype MP:0000001img reproductive system phenotype MP:000538910img abnormal sperm midpiece morphology MP:0009831
Genes (20)

Species:
human : 20
SpeciesGeneGeneIdGene NameEvidence
HumanDPY19L2283417dpy-19-like 2 (C. elegans)
Click here to display 20 evidence detail records.
HumanSLC26A8116369solute carrier family 26 (anion exchanger), member 8
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HumanNSUN779730NOP2/Sun domain family, member 7
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HumanGOPC57120golgi-associated PDZ and coiled-coil motif containing
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HumanMNS155329meiosis-specific nuclear structural 1
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HumanPAIP251247poly(A) binding protein interacting protein 2
INFERRED
HumanCNOT729883CCR4-NOT transcription complex, subunit 7
Click here to display 20 evidence detail records.
HumanAKAP48852A kinase (PRKA) anchor protein 4
Click here to display 20 evidence detail records.
HumanLRP87804low density lipoprotein receptor-related protein 8, apolipoprotein e receptor
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HumanVDAC37419voltage-dependent anion channel 3
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HumanTMF17110TATA element modulatory factor 1
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HumanTALDO16888transaldolase 1
Click here to display 20 evidence detail records.
HumanSEPP16414selenoprotein P, plasma, 1
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HumanRXRB6257retinoid X receptor, beta
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HumanPVRL25819poliovirus receptor-related 2 (herpesvirus entry mediator B)
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HumanPPP1CC5501protein phosphatase 1, catalytic subunit, gamma isozyme
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HumanSEPT45414septin 4
Click here to display 20 evidence detail records.
HumanODF14956outer dense fiber of sperm tails 1
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HumanAGFG13267ArfGAP with FG repeats 1
INFERRED
HumanGPX42879glutathione peroxidase 4
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XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0009832abnormal sperm mitochondrial sheath morphology0self