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Details
Link-It Detail - Jax Mouse Phenotype - abnormal palatine shelf morphology
Debug Stats
  • ### Total Build Time: 34 ms 79.829 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 396 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 293 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 183 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=5 ms Completed: 5 ms rowSize= 14 bytes
  • CONCEPT_NAMESPACE gt=NONE 1 ms Completed: 1 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=1 ms Completed: 1 ms rowSize= 1.031 KB
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 1.020 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=2 ms Completed: 2 ms rowSize= 5.607 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=21 ms Completed: 21 ms rowSize= 70.003 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.172 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal palatine shelf morphology MP:0004537
Definition (1)
any structural anomaly of the bony projection of the palatine bone that normally fuses with maxillary shelf to form secondary (hard) palate
Synonyms (1)
"abnormal horizontal plate" EXACT
Parents (2)
img abnormal palate bone morphology MP:0009891
img abnormal palatine bone morphology MP:0005249
Children (2)
img absent palatine shelf MP:0000431
img decreased palatine shelf size MP:0009895
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img digestive/alimentary phenotype MP:00053817img abnormal palate bone morphology MP:0009891
img mammalian phenotype MP:0000001img craniofacial phenotype MP:000538211img abnormal palate bone morphology MP:0009891
img mammalian phenotype MP:0000001img craniofacial phenotype MP:00053828img abnormal palatine bone morphology MP:0005249
img mammalian phenotype MP:0000001img skeleton phenotype MP:00053909img abnormal palatine bone morphology MP:0005249
Genes (27)

Species:
human : 27
Page Size
Current 25
  Page 1 of 2
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanRSPO2340419R-spondin 2
INFERRED
HumanARID5B84159AT rich interactive domain 5B (MRF1-like)
INFERRED
HumanCSRNP164651cysteine-serine-rich nuclear protein 1
INFERRED
HumanWDR1957728WD repeat domain 19
INFERRED
HumanPDSS257107prenyl (decaprenyl) diphosphate synthase, subunit 2
img Jax MP, Pubmed Id: 19086028, MOUSE PHENOTYPE ID: MGI:95524
img Jax MP, Pubmed Id: 11978771, MOUSE PHENOTYPE ID: MGI:95729
img Jax MP, Pubmed Id: 20503384, MOUSE PHENOTYPE ID: MGI:95523
img Jax MP, Pubmed Id: 9409679, MOUSE PHENOTYPE ID: MGI:1347481
img Jax MP, Pubmed Id: 12812790, MOUSE PHENOTYPE ID: MGI:1347479
img Jax MP, Pubmed Id: 19086028, MOUSE PHENOTYPE ID: MGI:95524
img Jax MP, Pubmed Id: 20196077, MOUSE PHENOTYPE ID: MGI:1859211
img Jax MP, Pubmed Id: 17610273, MOUSE PHENOTYPE ID: MGI:2178049
img Jax MP, Pubmed Id: 17610273, MOUSE PHENOTYPE ID: MGI:2447280
img Jax MP, Pubmed Id: 21871565, MOUSE PHENOTYPE ID: MGI:1918615
img Jax MP, Pubmed Id: 7440954, MOUSE PHENOTYPE ID: MGI:95483
HumanTBX2250945T-box 22
INFERRED
HumanSCHIP129970schwannomin interacting protein 1
INFERRED
HumanTIPARP25976TCDD-inducible poly(ADP-ribose) polymerase
INFERRED
HumanSGPL18879sphingosine-1-phosphate lyase 1
INFERRED
HumanPRRX15396paired related homeobox 1
INFERRED
HumanPAX95083paired box 9
INFERRED
HumanMSX14487msh homeobox 1
INFERRED
HumanMN14330meningioma (disrupted in balanced translocation) 1
INFERRED
HumanJAG23714jagged 2
INFERRED
HumanIRF63664interferon regulatory factor 6
img Jax MP, Pubmed Id: 20196077, MOUSE PHENOTYPE ID: MGI:1859211
img Jax MP, Pubmed Id: 17610273, MOUSE PHENOTYPE ID: MGI:2447280
img Jax MP, Pubmed Id: 20503384, MOUSE PHENOTYPE ID: MGI:95523
img Jax MP, Pubmed Id: 9409679, MOUSE PHENOTYPE ID: MGI:1347481
img Jax MP, Pubmed Id: 19086028, MOUSE PHENOTYPE ID: MGI:95524
img Jax MP, Pubmed Id: 7440954, MOUSE PHENOTYPE ID: MGI:95483
img Jax MP, Pubmed Id: 17610273, MOUSE PHENOTYPE ID: MGI:2178049
img Jax MP, Pubmed Id: 11978771, MOUSE PHENOTYPE ID: MGI:95729
img Jax MP, Pubmed Id: 21871565, MOUSE PHENOTYPE ID: MGI:1918615
img Jax MP, Pubmed Id: 12812790, MOUSE PHENOTYPE ID: MGI:1347479
img Jax MP, Pubmed Id: 19086028, MOUSE PHENOTYPE ID: MGI:95524
HumanGLI32737GLI family zinc finger 3
img Jax MP, Pubmed Id: 11978771, MOUSE PHENOTYPE ID: MGI:95729
img Jax MP, Pubmed Id: 7440954, MOUSE PHENOTYPE ID: MGI:95483
img Jax MP, Pubmed Id: 12812790, MOUSE PHENOTYPE ID: MGI:1347479
img Jax MP, Pubmed Id: 20196077, MOUSE PHENOTYPE ID: MGI:1859211
img Jax MP, Pubmed Id: 17610273, MOUSE PHENOTYPE ID: MGI:2178049
img Jax MP, Pubmed Id: 17610273, MOUSE PHENOTYPE ID: MGI:2447280
img Jax MP, Pubmed Id: 20503384, MOUSE PHENOTYPE ID: MGI:95523
img Jax MP, Pubmed Id: 19086028, MOUSE PHENOTYPE ID: MGI:95524
img Jax MP, Pubmed Id: 21871565, MOUSE PHENOTYPE ID: MGI:1918615
img Jax MP, Pubmed Id: 19086028, MOUSE PHENOTYPE ID: MGI:95524
img Jax MP, Pubmed Id: 9409679, MOUSE PHENOTYPE ID: MGI:1347481
HumanGLI22736GLI family zinc finger 2
INFERRED
HumanFOXC22303forkhead box C2 (MFH-1, mesenchyme forkhead 1)
img Jax MP, Pubmed Id: 21871565, MOUSE PHENOTYPE ID: MGI:1918615
img Jax MP, Pubmed Id: 19086028, MOUSE PHENOTYPE ID: MGI:95524
img Jax MP, Pubmed Id: 7440954, MOUSE PHENOTYPE ID: MGI:95483
img Jax MP, Pubmed Id: 20196077, MOUSE PHENOTYPE ID: MGI:1859211
img Jax MP, Pubmed Id: 12812790, MOUSE PHENOTYPE ID: MGI:1347479
img Jax MP, Pubmed Id: 11978771, MOUSE PHENOTYPE ID: MGI:95729
img Jax MP, Pubmed Id: 17610273, MOUSE PHENOTYPE ID: MGI:2178049
img Jax MP, Pubmed Id: 9409679, MOUSE PHENOTYPE ID: MGI:1347481
img Jax MP, Pubmed Id: 17610273, MOUSE PHENOTYPE ID: MGI:2447280
img Jax MP, Pubmed Id: 20503384, MOUSE PHENOTYPE ID: MGI:95523
img Jax MP, Pubmed Id: 19086028, MOUSE PHENOTYPE ID: MGI:95524
HumanFOXF22295forkhead box F2
img Jax MP, Pubmed Id: 12812790, MOUSE PHENOTYPE ID: MGI:1347479
img Jax MP, Pubmed Id: 20196077, MOUSE PHENOTYPE ID: MGI:1859211
img Jax MP, Pubmed Id: 17610273, MOUSE PHENOTYPE ID: MGI:2447280
img Jax MP, Pubmed Id: 19086028, MOUSE PHENOTYPE ID: MGI:95524
img Jax MP, Pubmed Id: 11978771, MOUSE PHENOTYPE ID: MGI:95729
img Jax MP, Pubmed Id: 20503384, MOUSE PHENOTYPE ID: MGI:95523
img Jax MP, Pubmed Id: 19086028, MOUSE PHENOTYPE ID: MGI:95524
img Jax MP, Pubmed Id: 9409679, MOUSE PHENOTYPE ID: MGI:1347481
img Jax MP, Pubmed Id: 17610273, MOUSE PHENOTYPE ID: MGI:2178049
img Jax MP, Pubmed Id: 21871565, MOUSE PHENOTYPE ID: MGI:1918615
img Jax MP, Pubmed Id: 7440954, MOUSE PHENOTYPE ID: MGI:95483
HumanFGFR22263fibroblast growth factor receptor 2
img Jax MP, Pubmed Id: 19086028, MOUSE PHENOTYPE ID: MGI:95524
img Jax MP, Pubmed Id: 11978771, MOUSE PHENOTYPE ID: MGI:95729
img Jax MP, Pubmed Id: 17610273, MOUSE PHENOTYPE ID: MGI:2447280
img Jax MP, Pubmed Id: 9409679, MOUSE PHENOTYPE ID: MGI:1347481
img Jax MP, Pubmed Id: 19086028, MOUSE PHENOTYPE ID: MGI:95524
img Jax MP, Pubmed Id: 7440954, MOUSE PHENOTYPE ID: MGI:95483
img Jax MP, Pubmed Id: 17610273, MOUSE PHENOTYPE ID: MGI:2178049
img Jax MP, Pubmed Id: 21871565, MOUSE PHENOTYPE ID: MGI:1918615
img Jax MP, Pubmed Id: 20503384, MOUSE PHENOTYPE ID: MGI:95523
img Jax MP, Pubmed Id: 20196077, MOUSE PHENOTYPE ID: MGI:1859211
img Jax MP, Pubmed Id: 12812790, MOUSE PHENOTYPE ID: MGI:1347479
HumanFGFR32261fibroblast growth factor receptor 3
img Jax MP, Pubmed Id: 19086028, MOUSE PHENOTYPE ID: MGI:95524
img Jax MP, Pubmed Id: 20503384, MOUSE PHENOTYPE ID: MGI:95523
img Jax MP, Pubmed Id: 19086028, MOUSE PHENOTYPE ID: MGI:95524
img Jax MP, Pubmed Id: 17610273, MOUSE PHENOTYPE ID: MGI:2178049
img Jax MP, Pubmed Id: 11978771, MOUSE PHENOTYPE ID: MGI:95729
img Jax MP, Pubmed Id: 20196077, MOUSE PHENOTYPE ID: MGI:1859211
img Jax MP, Pubmed Id: 7440954, MOUSE PHENOTYPE ID: MGI:95483
img Jax MP, Pubmed Id: 12812790, MOUSE PHENOTYPE ID: MGI:1347479
img Jax MP, Pubmed Id: 17610273, MOUSE PHENOTYPE ID: MGI:2447280
img Jax MP, Pubmed Id: 9409679, MOUSE PHENOTYPE ID: MGI:1347481
img Jax MP, Pubmed Id: 21871565, MOUSE PHENOTYPE ID: MGI:1918615
HumanEYA12138eyes absent homolog 1 (Drosophila)
INFERRED
HumanEDNRB1910endothelin receptor type B
INFERRED
HumanDLX51749distal-less homeobox 5
INFERRED
HumanDLX21746distal-less homeobox 2
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0004537abnormal palatine shelf morphology0self