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Details
Link-It Detail - Jax Mouse Phenotype - abnormal cell morphology
Debug Stats
  • ### Total Build Time: 531 ms 23.933 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 376 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
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  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.559 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=523 ms Completed: 523 ms rowSize= 15.874 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.162 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal cell morphology MP:0000358
Definition (1)
any structural anomaly of the minute protoplasmic masses that make up organized tissues and which are the fundamental structural and functional units of living organisms
Synonyms (1)
"cell abnormalities" BROAD
Parents (1)
img cellular phenotype MP:0005384
Children (8)
img abnormal plasma membrane morphology MP:0003950
img abnormal Golgi apparatus morphology MP:0011743
img abnormal endoplasmic reticulum morphology MP:0009378
img abnormal foam cell morphology MP:0009840
img abnormal cell nucleus morphology MP:0003111
img abnormal mitochondrion morphology MP:0006035
img abnormal lysosome morphology MP:0005058
img abnormal cell mass MP:0003902
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img cellular phenotype MP:00053843img cellular phenotype MP:0005384
Genes (357)

Species:
human : 357
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanRAD21L1642636RAD21-like 1 (S. pombe)
INFERRED
HumanCISD2493856CDGSH iron sulfur domain 2
INFERRED
HumanMIA3375056melanoma inhibitory activity family, member 3
Click here to display 141 evidence detail records.
HumanTHEM5284486thioesterase superfamily member 5
INFERRED
HumanPTRF284119polymerase I and transcript release factor
INFERRED
HumanAQP11282679aquaporin 11
INFERRED
HumanMCM9254394minichromosome maintenance complex component 9
INFERRED
HumanRNASEH1246243ribonuclease H1
INFERRED
HumanTDRD6221400tudor domain containing 6
Click here to display 141 evidence detail records.
HumanGPR116221395G protein-coupled receptor 116
INFERRED
HumanPLD6201164phospholipase D family, member 6
INFERRED
HumanPIKFYVE200576phosphoinositide kinase, FYVE finger containing
Click here to display 141 evidence detail records.
HumanESCO2157570establishment of sister chromatid cohesion N-acetyltransferase 2
INFERRED
HumanTTBK2146057tau tubulin kinase 2
Click here to display 141 evidence detail records.
HumanNEK7140609NIMA-related kinase 7
INFERRED
HumanPPARGC1B133522peroxisome proliferator-activated receptor gamma, coactivator 1 beta
INFERRED
HumanPIFO128344primary cilia formation
Click here to display 141 evidence detail records.
HumanTOP1MT116447topoisomerase (DNA) I, mitochondrial
INFERRED
HumanOMA1115209OMA1 zinc metallopeptidase
INFERRED
HumanPTPMT1114971protein tyrosine phosphatase, mitochondrial 1
INFERRED
HumanMOB1B92597MOB kinase activator 1B
INFERRED
HumanRASL10B91608RAS-like, family 10, member B
Click here to display 141 evidence detail records.
HumanPNPT187178polyribonucleotide nucleotidyltransferase 1
INFERRED
HumanMCM884515minichromosome maintenance complex component 8
INFERRED
HumanDOT1L84444DOT1-like histone H3K79 methyltransferase
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0000358abnormal cell morphology0self