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Details
Link-It Detail - Human Phenotype - Abnormality of the gastric mucosa
Debug Stats
  • ### Total Build Time: 23 ms 26.589 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 208 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=2 ms Completed: 2 ms rowSize= 447 bytes
  • CONCEPT_CHILDREN gt=1 ms Completed: 1 ms rowSize= 748 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=2 ms Completed: 2 ms rowSize= 2.090 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=14 ms Completed: 14 ms rowSize= 21.957 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.027 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the gastric mucosa HP:0004295
Parents (1)
img Abnormality of the stomach HP:0002577
Children (2)
img Gastritis HP:0005263
img Gastric ulcer HP:0002592
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of the stomach HP:0002577
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the stomach HP:0002577
Genes (38)

Species:
human : 38
Page Size
Current 25
  Page 1 of 2
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanCISD2493856CDGSH iron sulfur domain 2
img HP RolledUp, OMIM ID: 604928
HumanKIAA2022340533KIAA2022
img HP TAS, OMIM ID: 300524
HumanWBSCR22114049Williams Beuren syndrome chromosome region 22
img HP TAS, OMIM ID: 194050
HumanFERMT155612fermitin family member 1
img HP TAS, OMIM ID: 173650
HumanMLXIPL51085MLX interacting protein-like
img HP TAS, OMIM ID: 194050
HumanSLCO1B328234solute carrier organic anion transporter family, member 1B3
img HP TAS, OMIM ID: 237450
HumanSLCO1B110599solute carrier organic anion transporter family, member 1B1
img HP TAS, OMIM ID: 237450
HumanGTF2IRD19569GTF2I repeat domain containing 1
img HP TAS, OMIM ID: 194050
HumanHHC39151hypocalciuric hypercalcemia 3 (Oklahoma type)
img HP RolledUp, OMIM ID: 600740
HumanAIP9049aryl hydrocarbon receptor interacting protein
img HP TAS, OMIM ID: 219090
HumanBCL108915B-cell CLL/lymphoma 10
img HP TAS, OMIM ID: 137245
HumanTKCR7085torticollis, keloids, cryptorchidism and renal dysplasia
img HP TAS, OMIM ID: 314300
HumanPIK3CA5290phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit alpha
img HP RolledUp, OMIM ID: 137215
HumanMUTYH4595mutY homolog (E. coli)
img HP RolledUp, OMIM ID: 137215
HumanMEN14221multiple endocrine neoplasia I
img HP TAS, OMIM ID: 131100
HumanLBR3930lamin B receptor
img HP TAS, OMIM ID: 613471
HumanKRAS3845Kirsten rat sarcoma viral oncogene homolog
img HP RolledUp, OMIM ID: 137215
HumanIRF13659interferon regulatory factor 1
img HP RolledUp, OMIM ID: 137215
HumanIL1RN3557interleukin 1 receptor antagonist
img HP RolledUp, OMIM ID: 137215
HumanIL1B3553interleukin 1, beta
img HP RolledUp, OMIM ID: 137215
HumanHHC23086hypocalciuric hypercalcemia 2
img HP RolledUp, OMIM ID: 145981
HumanGTF2I2969general transcription factor IIi
img HP TAS, OMIM ID: 194050
HumanGNAS2778GNAS complex locus
img HP TAS, OMIM ID: 219090
HumanGNA112767guanine nucleotide binding protein (G protein), alpha 11 (Gq class)
img HP RolledUp, OMIM ID: 145981
HumanFGFR22263fibroblast growth factor receptor 2
img HP RolledUp, OMIM ID: 137215
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0004295Abnormality of the gastric mucosa0self