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Details
Link-It Detail - Jax Mouse Phenotype - iris hypoplasia
Debug Stats
  • ### Total Build Time: 16 ms 11.104 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 358 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 240 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=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= 579 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 579 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.566 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=11 ms Completed: 11 ms rowSize= 6.525 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.153 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
iris hypoplasia MP:0006226
Definition (1)
underdevelopment or reduced size of the iris, usually due to a reduced number of cells
Parents (1)
img abnormal iris morphology MP:0001322
Children (1)
img iris stroma hypoplasia MP:0006230
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img vision/eye phenotype MP:00053917img abnormal iris morphology MP:0001322
Genes (11)

Species:
human : 11
SpeciesGeneGeneIdGene NameEvidence
HumanSLC24A5283652solute carrier family 24 (sodium/potassium/calcium exchanger), member 5
Click here to display 19 evidence detail records.
HumanLGR455366leucine-rich repeat containing G protein-coupled receptor 4
Click here to display 19 evidence detail records.
HumanPITX25308paired-like homeodomain 2
Click here to display 19 evidence detail records.
HumanPAX65080paired box 6
Click here to display 19 evidence detail records.
HumanMITF4286microphthalmia-associated transcription factor
Click here to display 19 evidence detail records.
HumanLMX1B4010LIM homeobox transcription factor 1, beta
INFERRED
HumanHOXA133209homeobox A13
INFERRED
HumanFOXC22303forkhead box C2 (MFH-1, mesenchyme forkhead 1)
INFERRED
HumanFOXE32301forkhead box E3
Click here to display 19 evidence detail records.
HumanFOXC12296forkhead box C1
Click here to display 19 evidence detail records.
HumanBMP4652bone morphogenetic protein 4
Click here to display 19 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0006226iris hypoplasia0self