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Details
Link-It Detail - Human Phenotype - Abnormal localization of kidneys
Debug Stats
  • ### Total Build Time: 35 ms 29.625 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 207 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=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=4 ms Completed: 4 ms rowSize= 774 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 1.379 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=11 ms Completed: 11 ms rowSize= 3.942 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=13 ms Completed: 13 ms rowSize= 22.175 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.026 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormal localization of kidneys HP:0100542
Parents (2)
img Abnormality of the kidney HP:0000077
img Abnormal renal morphology HP:0012210
Children (4)
img Nephroptosis HP:0011126
img Ectopic kidney HP:0000086
img Horseshoe kidney HP:0000085
img Partially duplicated displaced kidney HP:0008738
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of the kidney HP:0000077
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the kidney HP:0000077
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormal renal morphology HP:0012210
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormal renal morphology HP:0012210
Genes (66)

Species:
human : 66
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanMMRFCGU100529147Microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations
img HP RolledUp, OMIM ID: 613680
HumanRCHTS100462676Roifman-Chitayat syndrome
img HP RolledUp, OMIM ID: 613328
HumanMICRODEL3Q29100188788Chromosome 3q29 microdeletion syndrome
img HP TAS, OMIM ID: 609425
HumanHFM170474Hemifacial microsomia
img HP TAS, OMIM ID: 164210
HumanESCO2157570establishment of sister chromatid cohesion N-acetyltransferase 2
img HP RolledUp, OMIM ID: 268300
HumanCCBE1147372collagen and calcium binding EGF domains 1
img HP TAS, OMIM ID: 235510
HumanWBSCR22114049Williams Beuren syndrome chromosome region 22
img HP TAS, OMIM ID: 194050
HumanCHST14113189carbohydrate (N-acetylgalactosamine 4-0) sulfotransferase 14
img HP TAS, OMIM ID: 601776
HumanFAM58A92002family with sequence similarity 58, member A
img HP TAS, OMIM ID: 300707
HumanSLX484464SLX4 structure-specific endonuclease subunit
img HP RolledUp, OMIM ID: 613951
HumanJAM383700junctional adhesion molecule 3
img HP RolledUp, OMIM ID: 613730
HumanVANGL181839VANGL planar cell polarity protein 1
img HP TAS, OMIM ID: 600145
HumanPORCN64840porcupine homolog (Drosophila)
img HP TAS, OMIM ID: 305600
HumanSTRA664220stimulated by retinoic acid 6
img HP TAS, OMIM ID: 601186
HumanSALL457167sal-like 4 (Drosophila)
img HP TAS, OMIM ID: 607323
HumanCHD755636chromodomain helicase DNA binding protein 7
img HP TAS, OMIM ID: 214800
HumanMLXIPL51085MLX interacting protein-like
img HP TAS, OMIM ID: 194050
HumanTBX2250945T-box 22
img HP TAS, OMIM ID: 302905
HumanTCTN326123tectonic family member 3
img HP RolledUp, OMIM ID: 614815
HumanNIPBL25836Nipped-B homolog (Drosophila)
img HP RolledUp, OMIM ID: 122470
HumanLEMD323592LEM domain containing 3
img HP TAS, OMIM ID: 166700
HumanSPINK511005serine peptidase inhibitor, Kazal type 5
img HP TAS, OMIM ID: 256500
HumanRAI110743retinoic acid induced 1
img HP TAS, OMIM ID: 182290
HumanCD9610225CD96 molecule
img HP TAS, OMIM ID: 211750
HumanAKT310000v-akt murine thymoma viral oncogene homolog 3
img HP TAS, OMIM ID: 603387
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0100542Abnormal localization of kidneys0self