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Details
Link-It Detail - Jax Mouse Phenotype - abnormal maxilla morphology
Debug Stats
  • ### Total Build Time: 106 ms 23.487 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 382 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 251 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 175 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= 578 bytes
  • CONCEPT_CHILDREN gt=5 ms Completed: 5 ms rowSize= 2.354 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.896 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=98 ms Completed: 98 ms rowSize= 15.573 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.165 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal maxilla morphology MP:0000455
Definition (1)
any structural anomaly of the upper bony framework of the mouth where the superior teeth are held
Synonyms (1)
"maxilla dysplasia" EXACT
Parents (1)
img abnormal jaw morphology MP:0000454
Children (5)
img absent maxilla MP:0004539
img small maxilla MP:0004540
img abnormal maxillary shelf morphology MP:0004538
img abnormal premaxilla morphology MP:0002820
img long maxilla MP:0011813
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img craniofacial phenotype MP:00053828img abnormal jaw morphology MP:0000454
img mammalian phenotype MP:0000001img skeleton phenotype MP:00053909img abnormal jaw morphology MP:0000454
Genes (100)

Species:
human : 100
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanRSPO2340419R-spondin 2
Click here to display 69 evidence detail records.
HumanSH3PXD2B285590SH3 and PX domains 2B
INFERRED
HumanGSC145258goosecoid homeobox
Click here to display 69 evidence detail records.
HumanPKDCC91461protein kinase domain containing, cytoplasmic
Click here to display 69 evidence detail records.
HumanSLC39A1391252solute carrier family 39 (zinc transporter), member 13
INFERRED
HumanZIC585416Zic family member 5
INFERRED
HumanDISP184976dispatched homolog 1 (Drosophila)
INFERRED
HumanARID5B84159AT rich interactive domain 5B (MRF1-like)
INFERRED
HumanFUZ80199fuzzy planar cell polarity protein
INFERRED
HumanNABP279035nucleic acid binding protein 2
INFERRED
HumanPRDM1663976PR domain containing 16
INFERRED
HumanALX460529ALX homeobox 4
Click here to display 69 evidence detail records.
HumanPLEKHA159338pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1
INFERRED
HumanWDR1957728WD repeat domain 19
Click here to display 69 evidence detail records.
HumanCTNNBIP156998catenin, beta interacting protein 1
INFERRED
HumanFAM20C56975family with sequence similarity 20, member C
Click here to display 69 evidence detail records.
HumanIFT5755081intraflagellar transport 57 homolog (Chlamydomonas)
Click here to display 69 evidence detail records.
HumanMKS154903Meckel syndrome, type 1
INFERRED
HumanBNC254796basonuclin 2
INFERRED
HumanCDON50937cell adhesion associated, oncogene regulated
Click here to display 69 evidence detail records.
HumanCHST1150515carbohydrate (chondroitin 4) sulfotransferase 11
INFERRED
HumanSCHIP129970schwannomin interacting protein 1
INFERRED
HumanFOXD327022forkhead box D3
INFERRED
HumanTIPARP25976TCDD-inducible poly(ADP-ribose) polymerase
INFERRED
HumanBRD423476bromodomain containing 4
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0000455abnormal maxilla morphology0self