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Details
Link-It Detail - Jax Mouse Phenotype - abnormal liver morphology
Debug Stats
  • ### Total Build Time: 2,875 ms 32.420 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 378 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 314 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 172 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 595 bytes
  • CONCEPT_CHILDREN gt=5 ms Completed: 5 ms rowSize= 12.309 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.592 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=2,863 ms Completed: 2.863 Seconds rowSize= 15.787 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.163 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal liver morphology MP:0000598
Definition (1)
any structural anomaly of the bile-secreting organ that is important for detoxification, for fat, carbohydrate, and protein metabolism, and for glycogen storage
Synonyms (1)
"abnormal liver" BROAD
Parents (1)
img abnormal hepatobiliary system morphology MP:0002138
Children (27)
img decreased liver triglyceride level MP:0009356
img absent liver MP:0011877
img hepatic necrosis MP:0001654
img increased liver glycogen level MP:0010400
img abnormal liver zinc level MP:0011924
img decreased susceptibility to hepatic steatosis MP:0002310
img liver hemorrhage MP:0003888
img abnormal liver development MP:0000596
img hepatic steatosis MP:0002628
img liver cysts MP:0003327
img abnormal liver iron level MP:0008738
img decreased liver free fatty acids level MP:0010360
img pale liver MP:0000603
img liver cirrhosis MP:0003046
img liver abscess MP:0003332
img abnormal liver parenchyma morphology MP:0008986
img abnormal intrahepatic bile duct morphology MP:0009497
img abnormal liver size MP:0004848
img liver degeneration MP:0003103
img increased liver triglyceride level MP:0009355
img decreased liver cholesterol level MP:0010026
img decreased liver glycogen level MP:0010398
img increased liver cholesterol level MP:0010027
img abnormal liver copper level MP:0003065
img liver fibrosis MP:0003333
img herniated liver MP:0010912
img abnormal liver vasculature morphology MP:0009820
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img liver/biliary system phenotype MP:00053704img abnormal hepatobiliary system morphology MP:0002138
Genes (764)

Species:
human : 764
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SpeciesGeneGeneIdGene NameEvidence
HumanGIMAP1-GIMAP5100527949
Click here to display 321 evidence detail records.
HumanCCR2729230chemokine (C-C motif) receptor 2
INFERRED
HumanNCF1653361neutrophil cytosolic factor 1
INFERRED
HumanCFC1B653275cripto, FRL-1, cryptic family 1B
Click here to display 321 evidence detail records.
HumanPLIN5440503perilipin 5
INFERRED
HumanEIF2AK4440275eukaryotic translation initiation factor 2 alpha kinase 4
INFERRED
HumanNHLRC1378884NHL repeat containing 1
INFERRED
HumanFFAR4338557free fatty acid receptor 4
INFERRED
HumanTHEM5284486thioesterase superfamily member 5
INFERRED
HumanSLC13A5284111solute carrier family 13 (sodium-dependent citrate transporter), member 5
Click here to display 321 evidence detail records.
HumanAQP11282679aquaporin 11
INFERRED
HumanNEGR1257194neuronal growth regulator 1
INFERRED
HumanPTF1A256297pancreas specific transcription factor, 1a
INFERRED
HumanRICTOR253260RPTOR independent companion of MTOR, complex 2
INFERRED
HumanGPRC6A222545G protein-coupled receptor, family C, group 6, member A
INFERRED
HumanCYS1192668cystin 1
INFERRED
HumanDHX36170506DEAH (Asp-Glu-Ala-His) box polypeptide 36
INFERRED
HumanBHLHA15168620basic helix-loop-helix family, member a15
INFERRED
HumanSGMS2166929sphingomyelin synthase 2
INFERRED
HumanTMPRSS6164656transmembrane protease, serine 6
INFERRED
HumanZFPM1161882zinc finger protein, FOG family member 1
INFERRED
HumanRDH10157506retinol dehydrogenase 10 (all-trans)
INFERRED
HumanKLB152831klotho beta
Click here to display 321 evidence detail records.
HumanCOMMD1150684copper metabolism (Murr1) domain containing 1
INFERRED
HumanLIPI149998lipase, member I
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0000598abnormal liver morphology0self