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Details
Link-It Detail - Human Phenotype - Abnormality of salivation
Debug Stats
  • ### Total Build Time: 23 ms 22.822 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 200 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=3 ms Completed: 3 ms rowSize= 451 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 1.053 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.166 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=12 ms Completed: 12 ms rowSize= 18.804 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.020 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of salivation HP:0100755
Parents (1)
img Abnormality of the oral cavity HP:0000163
Children (3)
img Xerostomia HP:0000217
img Excessive salivation HP:0003781
img Reduced salivation HP:0100756
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of the oral cavity HP:0000163
Genes (41)

Species:
human : 41
Page Size
Current 25
  Page 1 of 2
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanECT100379198centralopathic epilepsy
HumanTUBB2B347733tubulin, beta 2B class IIb
img HP RolledUp, OMIM ID: 610031
HumanNOD264127nucleotide-binding oligomerization domain containing 2
img HP RolledUp, OMIM ID: 186580
HumanMRXSL57790Lubs X-linked mental retardation syndrome
HumanALS257679amyotrophic lateral sclerosis 2 (juvenile)
img HP RolledUp, OMIM ID: 205100
HumanZC4H255906zinc finger, C4H2 domain containing
img HP RolledUp, OMIM ID: 314580
HumanPOLR3B55703polymerase (RNA) III (DNA directed) polypeptide B
img HP RolledUp, OMIM ID: 607694
HumanFERMT155612fermitin family member 1
img HP RolledUp, OMIM ID: 173650
HumanAP4E123431adaptor-related protein complex 4, epsilon 1 subunit
img HP RolledUp, OMIM ID: 613744
HumanVPS13A23230vacuolar protein sorting 13 homolog A (S. cerevisiae)
HumanSPG2023111spastic paraplegia 20 (Troyer syndrome)
HumanPOLR3A11128polymerase (RNA) III (DNA directed) polypeptide A, 155kDa
img HP RolledUp, OMIM ID: 607694
HumanSLC9A610479solute carrier family 9, subfamily A (NHE6, cation proton antiporter 6), member 6
HumanZEB29839zinc finger E-box binding homeobox 2
HumanNRXN19378neurexin 1
img HP RolledUp, OMIM ID: 614325
HumanCRLF19244cytokine receptor-like factor 1
img HP RolledUp, OMIM ID: 601378
HumanAP4M19179adaptor-related protein complex 4, mu 1 subunit
HumanTP638626tumor protein p63
img HP RolledUp, OMIM ID: 604292
HumanUBE3A7337ubiquitin protein ligase E3A
img HP RolledUp, OMIM ID: 105830
HumanTHM7063thymoma
img HP RolledUp, OMIM ID: 274230
HumanCDKL56792cyclin-dependent kinase-like 5
img HP RolledUp, OMIM ID: 105830
HumanSLC16A26567solute carrier family 16, member 2 (thyroid hormone transporter)
HumanSCN9A6335sodium channel, voltage-gated, type IX, alpha subunit
img HP RolledUp, OMIM ID: 133020
HumanPRPS15631phosphoribosyl pyrophosphate synthetase 1
img HP RolledUp, OMIM ID: 301835
HumanPAK35063p21 protein (Cdc42/Rac)-activated kinase 3
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0100755Abnormality of salivation0self