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Details
Link-It Detail - Human Phenotype - Abnormality of the fingertips
Debug Stats
  • ### Total Build Time: 66 ms 30.389 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 204 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=6 ms Completed: 6 ms rowSize= 442 bytes
  • CONCEPT_CHILDREN gt=6 ms Completed: 6 ms rowSize= 1.366 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=27 ms Completed: 27 ms rowSize= 3.928 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=23 ms Completed: 23 ms rowSize= 23.296 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.023 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the fingertips HP:0001211
Parents (1)
img Abnormality of finger HP:0001167
Children (4)
img Prominent fingertip pads HP:0001212
img Clubbing HP:0001217
img Clubbing of fingers HP:0100759
img Broad fingertip HP:0011300
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:000011810img Abnormality of finger HP:0001167
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of finger HP:0001167
img All HP:0000001img Phenotypic abnormality HP:00001189img Abnormality of finger HP:0001167
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of finger HP:0001167
Genes (40)

Species:
human : 40
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanPDA1100996949Patent ductus arteriosus, susceptibility to
img HP RolledUp, OMIM ID: 607411
HumanDEL17Q21.31791085
img HP RolledUp, OMIM ID: 610443
HumanSFTPA2729238surfactant protein A2
img HP RolledUp, OMIM ID: 178500
HumanMUC5B727897mucin 5B, oligomeric mucus/gel-forming
img HP RolledUp, OMIM ID: 178500
HumanSFTPA1653509surfactant protein A1
img HP RolledUp, OMIM ID: 178500
HumanKANSL1284058KAT8 regulatory NSL complex subunit 1
img HP RolledUp, OMIM ID: 610443
HumanELMOD2255520ELMO/CED-12 domain containing 2
img HP RolledUp, OMIM ID: 178500
HumanRHBDF279651rhomboid 5 homolog 2 (Drosophila)
img HP RolledUp, OMIM ID: 148500
HumanNSD164324nuclear receptor binding SET domain protein 1
img HP RolledUp, OMIM ID: 277590
HumanSMARCAD156916SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1
img HP RolledUp, OMIM ID: 136000
HumanABCA1226154ATP-binding cassette, sub-family A (ABC1), member 12
img HP RolledUp, OMIM ID: 601277
HumanGJB610804gap junction protein, beta 6, 30kDa
img HP RolledUp, OMIM ID: 129500
HumanMED129968mediator complex subunit 12
img HP RolledUp, OMIM ID: 305450
HumanPIGL9487phosphatidylinositol glycan anchor biosynthesis, class L
img HP RolledUp, OMIM ID: 280000
HumanKMT2D8085lysine (K)-specific methyltransferase 2D
img HP RolledUp, OMIM ID: 147920
HumanKDM6A7403lysine (K)-specific demethylase 6A
img HP RolledUp, OMIM ID: 147920
img HP RolledUp, OMIM ID: 300867
HumanTOC7149tylosis with oesophageal cancer
img HP RolledUp, OMIM ID: 148500
HumanTERT7015telomerase reverse transcriptase
img HP RolledUp, OMIM ID: 178500
HumanTERC7012telomerase RNA component
img HP RolledUp, OMIM ID: 178500
HumanTCF46925transcription factor 4
img HP RolledUp, OMIM ID: 610954
HumanSTK116794serine/threonine kinase 11
img HP RolledUp, OMIM ID: 175200
HumanSMARCA26595SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2
img HP RolledUp, OMIM ID: 601358
HumanSLCO2A16578solute carrier organic anion transporter family, member 2A1
img HP RolledUp, OMIM ID: 614441
HumanSFTPC6440surfactant protein C
img HP RolledUp, OMIM ID: 610913
img HP RolledUp, OMIM ID: 265120
img HP RolledUp, OMIM ID: 178500
HumanSFTPB6439surfactant protein B
img HP RolledUp, OMIM ID: 265120
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0001211Abnormality of the fingertips0self