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Details
Link-It Detail - Human Phenotype - Abnormal pancreas size
Debug Stats
  • ### Total Build Time: 23 ms 13.344 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 197 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=5 ms Completed: 5 ms rowSize= 455 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 782 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 1.170 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=8 ms Completed: 8 ms rowSize= 9.612 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.017 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormal pancreas size HP:0012094
Parents (1)
img Abnormality of pancreas morphology HP:0012090
Children (2)
img Aplasia/Hypoplasia of the pancreas HP:0100800
img Pancreatic hyperplasia HP:0006277
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of pancreas morphology HP:0012090
Genes (13)

Species:
human : 13
SpeciesGeneGeneIdGene NameEvidence
HumanDEL17Q12100884130Chromosome 17q12 deletion syndrome
img HP RolledUp, OMIM ID: 614527
HumanH19283120H19, imprinted maternally expressed transcript (non-protein coding)
img HP RolledUp, OMIM ID: 130650
HumanRFX6222546regulatory factor X, 6
HumanNSD164324nuclear receptor binding SET domain protein 1
img HP RolledUp, OMIM ID: 130650
HumanSTRA664220stimulated by retinoic acid 6
img HP RolledUp, OMIM ID: 601186
HumanKCNQ1OT110984KCNQ1 opposite strand/antisense transcript 1 (non-protein coding)
img HP RolledUp, OMIM ID: 130650
HumanEIF2AK39451eukaryotic translation initiation factor 2-alpha kinase 3
img HP RolledUp, OMIM ID: 226980
HumanHNF1B6928HNF1 homeobox B
img HP RolledUp, OMIM ID: 137920
HumanKCNQ13784potassium voltage-gated channel, KQT-like subfamily, member 1
img HP RolledUp, OMIM ID: 130650
HumanPDX13651pancreatic and duodenal homeobox 1
HumanIGF23481insulin-like growth factor 2 (somatomedin A)
img HP RolledUp, OMIM ID: 130650
HumanGATA62627GATA binding protein 6
HumanCDKN1C1028cyclin-dependent kinase inhibitor 1C (p57, Kip2)
img HP RolledUp, OMIM ID: 130650
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0012094Abnormal pancreas size0self