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Details
Link-It Detail - Human Phenotype - Abnormality of cation homeostasis
Debug Stats
  • ### Total Build Time: 33 ms 27.736 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 208 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 206 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= 451 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 1.160 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 1.166 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=19 ms Completed: 19 ms rowSize= 23.394 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.027 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of cation homeostasis HP:0010929
Definition (1)
An abnormality of `cation homeostasis` (GO:0055080).
Parents (1)
img Abnormality of ion homeostasis HP:0003111
Children (3)
img Abnormality of transition element cation homeostasis HP:0011030
img Abnormality of divalent inorganic cation homeostasis HP:0010927
img Abnormality of monovalent inorganic cation homeostasis HP:0010930
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of ion homeostasis HP:0003111
Genes (164)

Species:
human : 164
Page Size
Current 25
  Page 1 of 7
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanDEL2P21100415942Hypotonia-cystinuria syndrome
img HP RolledUp, OMIM ID: 606407
HumanHPRHP100188880Hypophosphatemic rickets and hyperparathyroidism
HumanCFSS100188773craniofacioskeletal syndrome
HumanLCRB387281locus control region, beta
img HP RolledUp, OMIM ID: 613985
HumanUBR1197131ubiquitin protein ligase E3 component n-recognin 1
img HP RolledUp, OMIM ID: 243800
HumanGNAS-AS1149775
HumanCLDN19149461claudin 19
img HP RolledUp, OMIM ID: 248190
HumanHFE2148738hemochromatosis type 2 (juvenile)
img HP RolledUp, OMIM ID: 602390
HumanCCBE1147372collagen and calcium binding EGF domains 1
img HP RolledUp, OMIM ID: 235510
HumanSLC34A3142680solute carrier family 34 (type II sodium/phosphate contransporter), member 3
img HP RolledUp, OMIM ID: 241530
HumanTRPM6140803transient receptor potential cation channel, subfamily M, member 6
HumanWBSCR22114049Williams Beuren syndrome chromosome region 22
img HP RolledUp, OMIM ID: 194050
HumanPUS180324pseudouridylate synthase 1
HumanCDC7379577cell division cycle 73
img HP RolledUp, OMIM ID: 145001
img HP RolledUp, OMIM ID: 145000
img HP RolledUp, OMIM ID: 608266
HumanWNK465266WNK lysine deficient protein kinase 4
img HP RolledUp, OMIM ID: 145260
img HP RolledUp, OMIM ID: 614491
HumanFRTS65211Fanconi renotubular syndrome
img HP RolledUp, OMIM ID: 134600
HumanWNK165125WNK lysine deficient protein kinase 1
img HP RolledUp, OMIM ID: 145260
img HP RolledUp, OMIM ID: 614492
HumanNOD264127nucleotide-binding oligomerization domain containing 2
img HP RolledUp, OMIM ID: 181000
HumanFAM111A63901family with sequence similarity 111, member A
img HP RolledUp, OMIM ID: 602361
img HP RolledUp, OMIM ID: 127000
HumanHAMP57817hepcidin antimicrobial peptide
img HP RolledUp, OMIM ID: 613313
img HP RolledUp, OMIM ID: 602390
HumanBTNL256244butyrophilin-like 2 (MHC class II associated)
img HP RolledUp, OMIM ID: 181000
HumanADCY1055811adenylate cyclase 10 (soluble)
img HP RolledUp, OMIM ID: 143870
HumanIFT12255764intraflagellar transport 122 homolog (Chlamydomonas)
img HP RolledUp, OMIM ID: 218330
HumanTMEM12755654transmembrane protein 127
img HP RolledUp, OMIM ID: 171300
HumanCHD755636chromodomain helicase DNA binding protein 7
img HP RolledUp, OMIM ID: 214800
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0010929Abnormality of cation homeostasis0self