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Details
Link-It Detail - Jax Mouse Phenotype - abnormal craniofacial development
Debug Stats
  • ### Total Build Time: 195 ms 27.325 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 394 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 211 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
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  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 587 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 7.954 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.576 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=188 ms Completed: 188 ms rowSize= 15.315 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.171 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal craniofacial development MP:0003935
Definition (1)
anomaly in the process of forming the face and/or cranium
Parents (1)
img abnormal craniofacial morphology MP:0000428
Children (17)
img abnormal Meckel's cartilage morphology MP:0005587
img abnormal medial nasal prominence morphology MP:0009903
img abnormal nasal capsule morphology MP:0004726
img abnormal nasal placode morphology MP:0006292
img abnormal lateral nasal prominence morphology MP:0009902
img craniofacial asymmetry MP:0008863
img abnormal mandibular prominence morphology MP:0010939
img abnormal palate development MP:0009653
img abnormal Reichert's cartilage morphology MP:0004915
img abnormal head mesenchyme morphology MP:0011260
img abnormal maxillary prominence morphology MP:0010940
img abnormal nasal pit morphology MP:0006306
img abnormal tooth development MP:0000116
img abnormal otic placode morphology MP:0011173
img abnormal branchial arch morphology MP:0002884
img abnormal frontonasal prominence morphology MP:0009901
img abnormal otic pit morphology MP:0011172
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img craniofacial phenotype MP:00053824img abnormal craniofacial morphology MP:0000428
Genes (305)

Species:
human : 305
Page Size
Current 25
  Page 1 of 13
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanCOMMD3-BMI1100532731
INFERRED
HumanLHX8431707LIM homeobox 8
INFERRED
HumanTBX10347853T-box 10
INFERRED
HumanRSPO2340419R-spondin 2
INFERRED
HumanBMPER168667BMP binding endothelial regulator
INFERRED
HumanNKX2-3159296
INFERRED
HumanRDH10157506retinol dehydrogenase 10 (all-trans)
Click here to display 90 evidence detail records.
HumanGSC145258goosecoid homeobox
INFERRED
HumanTRPM6140803transient receptor potential cation channel, subfamily M, member 6
Click here to display 90 evidence detail records.
HumanSLC32A1140679solute carrier family 32 (GABA vesicular transporter), member 1
INFERRED
HumanOSR2116039odd-skipped related 2 (Drosophila)
INFERRED
HumanPKDCC91461protein kinase domain containing, cytoplasmic
INFERRED
HumanDISP184976dispatched homolog 1 (Drosophila)
INFERRED
HumanTMEM10784314transmembrane protein 107
INFERRED
HumanANTXR184168anthrax toxin receptor 1
INFERRED
HumanMIXL183881Mix paired-like homeobox
INFERRED
HumanCCM283605cerebral cavernous malformation 2
INFERRED
HumanSP680320Sp6 transcription factor
INFERRED
HumanFUZ80199fuzzy planar cell polarity protein
INFERRED
HumanPGAP180055post-GPI attachment to proteins 1
INFERRED
HumanWLS79971wntless homolog (Drosophila)
Click here to display 90 evidence detail records.
HumanBCL11B64919B-cell CLL/lymphoma 11B (zinc finger protein)
INFERRED
HumanPRDM1663976PR domain containing 16
INFERRED
HumanALX460529ALX homeobox 4
INFERRED
HumanOVOL258495ovo-like 2 (Drosophila)
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0003935abnormal craniofacial development0self