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Details
Link-It Detail - Human Phenotype - Abdominal situs inversus
Debug Stats
  • ### Total Build Time: 43 ms 27.504 KB
  • CONCEPT_NAME gt=4 ms Completed: 4 ms rowSize= 199 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=9 ms Completed: 9 ms rowSize= 789 bytes
  • CONCEPT_CHILDREN gt=5 ms Completed: 5 ms rowSize= 445 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.103 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=22 ms Completed: 22 ms rowSize= 22.839 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.019 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abdominal situs inversus HP:0003363
Parents (2)
img Abnormality of abdominal situs HP:0011620
img Abnormality of the abdominal organs HP:0002012
Children (1)
img Situs inversus totalis HP:0001696
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of abdominal situs HP:0011620
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of the abdominal organs HP:0002012
Genes (37)

Species:
human : 37
Page Size
Current 25
  Page 1 of 2
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanCCDC103388389coiled-coil domain containing 103
img HP RolledUp, OMIM ID: 614679
HumanDNAAF3352909dynein, axonemal, assembly factor 3
img HP RolledUp, OMIM ID: 606763
HumanCCDC39339829coiled-coil domain containing 39
img HP RolledUp, OMIM ID: 613807
HumanCCDC11220136coiled-coil domain containing 11
img HP IEA, OMIM ID: 614779
HumanLATD207115Laterality defects, autosomal dominant
img HP RolledUp, OMIM ID: 601086
HumanUBR1197131ubiquitin protein ligase E3 component n-recognin 1
img HP RolledUp, OMIM ID: 243800
HumanEVC2132884Ellis van Creveld syndrome 2
img HP RolledUp, OMIM ID: 225500
HumanDNAAF1123872dynein, axonemal, assembly factor 1
img HP RolledUp, OMIM ID: 613193
HumanCCDC11493233coiled-coil domain containing 114
img HP RolledUp, OMIM ID: 615067
HumanDNAL183544dynein, axonemal, light chain 1
img HP RolledUp, OMIM ID: 614017
HumanDNAI264446dynein, axonemal, intermediate chain 2
img HP RolledUp, OMIM ID: 612444
HumanCILD256162ciliary dyskinesia, primary 2
img HP RolledUp, OMIM ID: 606763
HumanCFC155997cripto, FRL-1, cryptic family 1
img HP TAS, OMIM ID: 605376
HumanDNAAF255172dynein, axonemal, assembly factor 2
img HP RolledUp, OMIM ID: 612518
HumanCCDC4055036coiled-coil domain containing 40
img HP RolledUp, OMIM ID: 613808
HumanHEATR254919HEAT repeat containing 2
img HP RolledUp, OMIM ID: 614874
HumanINVS27130inversin
img HP RolledUp, OMIM ID: 602088
HumanNPHP327031nephronophthisis 3 (adolescent)
img HP ITM, OMIM ID: 208540
HumanDNAI127019dynein, axonemal, intermediate chain 1
img HP IEA, OMIM ID: 244400
HumanLRRC623639leucine rich repeat containing 6
img HP RolledUp, OMIM ID: 614935
HumanZNF42323090zinc finger protein 423
img HP RolledUp, OMIM ID: 614844
HumanSLC19A210560solute carrier family 19 (thiamine transporter), member 2
img HP ITM, OMIM ID: 249270
HumanZMPSTE2410269zinc metallopeptidase STE24
img HP RolledUp, OMIM ID: 275210
HumanPQBP110084polyglutamine binding protein 1
img HP TAS, OMIM ID: 309500
HumanDNAH118701dynein, axonemal, heavy chain 11
img HP IEA, OMIM ID: 270100
img HP RolledUp, OMIM ID: 611884
img HP IEA, OMIM ID: 244400
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0003363Abdominal situs inversus0self