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Details
Link-It Detail - Jax Mouse Phenotype - abnormal hepatobiliary system development
Debug Stats
  • ### Total Build Time: 36 ms 19.471 KB
  • CONCEPT_NAME gt=15 ms Completed: 15 ms rowSize= 410 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 228 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 199 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=0 Completed: 0 ms rowSize= 595 bytes
  • CONCEPT_CHILDREN gt=5 ms Completed: 5 ms rowSize= 1.025 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.592 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=14 ms Completed: 14 ms rowSize= 14.132 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.179 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal hepatobiliary system development MP:0003943
Definition (1)
developmental anomaly of any of the tissues of the liver or biliary system
Synonyms (1)
"abnormal liver/biliary system development" EXACT
Parents (1)
img abnormal hepatobiliary system morphology MP:0002138
Children (2)
img abnormal bile duct development MP:0002929
img abnormal liver development MP:0000596
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img liver/biliary system phenotype MP:00053704img abnormal hepatobiliary system morphology MP:0002138
Genes (66)

Species:
human : 66
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanGIMAP1-GIMAP5100527949
INFERRED
HumanGPBAR1151306G protein-coupled bile acid receptor 1
INFERRED
HumanSOX1764321SRY (sex determining region Y)-box 17
INFERRED
HumanPNPLA257104patatin-like phospholipase domain containing 2
INFERRED
HumanMKS154903Meckel syndrome, type 1
INFERRED
HumanMBTD154799mbt domain containing 1
INFERRED
HumanB9D127077B9 protein domain 1
INFERRED
HumanBRD123774bromodomain containing 1
INFERRED
HumanICMT23463isoprenylcysteine carboxyl methyltransferase
INFERRED
HumanRPGRIP1L23322RPGRIP1-like
INFERRED
HumanNCOA623054nuclear receptor coactivator 6
INFERRED
HumanYAP110413Yes-associated protein 1
INFERRED
HumanDNM1L10059dynamin 1-like
INFERRED
HumanFAM20B9917family with sequence similarity 20, member B
INFERRED
HumanRAPGEF29693Rap guanine nucleotide exchange factor (GEF) 2
INFERRED
HumanONECUT29480one cut homeobox 2
INFERRED
HumanPEX11B8799peroxisomal biogenesis factor 11 beta
INFERRED
HumanNPRL38131nitrogen permease regulator-like 3 (S. cerevisiae)
INFERRED
HumanXBP17494X-box binding protein 1
INFERRED
HumanWT17490Wilms tumor 1
INFERRED
HumanVEGFA7422vascular endothelial growth factor A
INFERRED
HumanUBC7316ubiquitin C
INFERRED
HumanTGFBR37049transforming growth factor, beta receptor III
INFERRED
HumanTGFB17040transforming growth factor, beta 1
INFERRED
HumanTCEB36924transcription elongation factor B (SIII), polypeptide 3 (110kDa, elongin A)
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0003943abnormal hepatobiliary system development0self