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Details
Link-It Detail - Human Phenotype - Abnormality of magnesium homeostasis
Debug Stats
  • ### Total Build Time: 38 ms 18.485 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 211 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_DEFINITION gt=NONE 0 Completed: 0 ms rowSize= 0 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=5 ms Completed: 5 ms rowSize= 813 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 1.061 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=8 ms Completed: 8 ms rowSize= 2.126 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=9 ms Completed: 9 ms rowSize= 13.124 KB
  • CONCEPT_XREFS gt=8 ms Completed: 8 ms rowSize= 1.030 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of magnesium homeostasis HP:0004921
Parents (2)
img Abnormality of metabolism/homeostasis HP:0001939
img Abnormality of divalent inorganic cation homeostasis HP:0010927
Children (3)
img Low to low-normal magnesium HP:0008274
img Hypomagnesemia HP:0002917
img Hypermagnesemia HP:0002918
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001184img Abnormality of metabolism/homeostasis HP:0001939
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of divalent inorganic cation homeostasis HP:0010927
Genes (16)

Species:
human : 16
SpeciesGeneGeneIdGene NameEvidence
HumanCLDN19149461claudin 19
img HP RolledUp, OMIM ID: 248190
HumanTRPM6140803transient receptor potential cation channel, subfamily M, member 6
img HP RolledUp, OMIM ID: 602014
HumanSARS254938seryl-tRNA synthetase 2, mitochondrial
img HP RolledUp, OMIM ID: 613845
HumanCLDN1610686claudin 16
img HP RolledUp, OMIM ID: 248250
HumanHHC39151hypocalciuric hypercalcemia 3 (Oklahoma type)
img HP RolledUp, OMIM ID: 600740
HumanTBCE6905tubulin folding cofactor E
img HP IEA, OMIM ID: 244460
HumanSLC12A36559solute carrier family 12 (sodium/chloride transporter), member 3
img HP RolledUp, OMIM ID: 263800
HumanSLC12A16557solute carrier family 12 (sodium/potassium/chloride transporter), member 1
img HP RolledUp, OMIM ID: 601678
HumanKCNJ103766potassium inwardly-rectifying channel, subfamily J, member 10
img HP RolledUp, OMIM ID: 612780
HumanKCNJ13758potassium inwardly-rectifying channel, subfamily J, member 1
img HP RolledUp, OMIM ID: 241200
HumanHHC23086hypocalciuric hypercalcemia 2
img HP RolledUp, OMIM ID: 145981
HumanGNA112767guanine nucleotide binding protein (G protein), alpha 11 (Gq class)
img HP RolledUp, OMIM ID: 145981
HumanEGF1950epidermal growth factor
img HP RolledUp, OMIM ID: 611718
HumanAP2S11175adaptor-related protein complex 2, sigma 1 subunit
img HP RolledUp, OMIM ID: 600740
HumanCASR846calcium-sensing receptor
img HP RolledUp, OMIM ID: 145980
HumanFXYD2486FXYD domain containing ion transport regulator 2
img HP RolledUp, OMIM ID: 154020
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0004921Abnormality of magnesium homeostasis0self