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Details
Link-It Detail - Human Phenotype - Abnormality of pancreas physiology
Debug Stats
  • ### Total Build Time: 23 ms 24.715 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 209 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 197 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=0 Completed: 0 ms rowSize= 448 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 1.431 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.163 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=15 ms Completed: 15 ms rowSize= 20.114 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.028 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of pancreas physiology HP:0012091
Definition (1)
An anomaly of the function of the pancreas.
Parents (1)
img Abnormality of the pancreas HP:0001732
Children (4)
img Abnormality of exocrine pancreas physiology HP:0012092
img Pancreatitis HP:0001733
img Exocrine pancreatic insufficiency HP:0001738
img Abnormality of endocrine pancreas physiology HP:0012093
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of the pancreas HP:0001732
Genes (84)

Species:
human : 84
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanWG474168Wegener granulomatosis
img HP RolledUp, OMIM ID: 608710
HumanH19283120H19, imprinted maternally expressed transcript (non-protein coding)
img HP RolledUp, OMIM ID: 130650
HumanITS282551Insulinoma tumor suppressor gene locus
img HP RolledUp, OMIM ID: 606960
HumanUBR1197131ubiquitin protein ligase E3 component n-recognin 1
img HP RolledUp, OMIM ID: 243800
HumanARX170302aristaless related homeobox
img HP RolledUp, OMIM ID: 300215
HumanDIS3L2129563DIS3 mitotic control homolog (S. cerevisiae)-like 2
HumanCDC7379577cell division cycle 73
HumanNSD164324nuclear receptor binding SET domain protein 1
img HP RolledUp, OMIM ID: 130650
HumanXPNPEP363929X-prolyl aminopeptidase (aminopeptidase P) 3, putative
img HP RolledUp, OMIM ID: 613159
HumanSBDS51119Shwachman-Bodian-Diamond syndrome
img HP RolledUp, OMIM ID: 260400
HumanBSCL226580Berardinelli-Seip congenital lipodystrophy 2 (seipin)
HumanCTRC11330chymotrypsin C (caldecrin)
img HP RolledUp, OMIM ID: 167800
HumanKCNQ1OT110984KCNQ1 opposite strand/antisense transcript 1 (non-protein coding)
img HP RolledUp, OMIM ID: 130650
HumanAGPAT2105551-acylglycerol-3-phosphate O-acyltransferase 2
HumanSLC25A1310165solute carrier family 25 (aspartate/glutamate carrier), member 13
img HP RolledUp, OMIM ID: 603471
HumanEIF2AK39451eukaryotic translation initiation factor 2-alpha kinase 3
img HP RolledUp, OMIM ID: 226980
HumanHHC39151hypocalciuric hypercalcemia 3 (Oklahoma type)
img HP RolledUp, OMIM ID: 600740
HumanSLC7A79056solute carrier family 7 (amino acid transporter light chain, y+L system), member 7
img HP RolledUp, OMIM ID: 222700
HumanOFD18481oral-facial-digital syndrome 1
img HP RolledUp, OMIM ID: 311200
HumanTGFB17040transforming growth factor, beta 1
img HP RolledUp, OMIM ID: 219700
HumanHNF1B6928HNF1 homeobox B
img HP RolledUp, OMIM ID: 137920
HumanABCC86833ATP-binding cassette, sub-family C (CFTR/MRP), member 8
HumanSPINK16690serine peptidase inhibitor, Kazal type 1
img HP RolledUp, OMIM ID: 167800
HumanSLC16A16566solute carrier family 16 (monocarboxylate transporter), member 1
HumanREG1A5967regenerating islet-derived 1 alpha
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0012091Abnormality of pancreas physiology0self