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Details
Link-It Detail - Jax Mouse Phenotype - abnormal facial morphology
Debug Stats
  • ### Total Build Time: 262 ms 22.062 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 380 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 188 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=0 Completed: 0 ms rowSize= 579 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 2.823 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.568 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=253 ms Completed: 253 ms rowSize= 15.241 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.164 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal facial morphology MP:0003743
Definition (1)
any structural anomaly of the face
Parents (1)
img abnormal head morphology MP:0000432
Children (6)
img abnormal nose morphology MP:0002233
img abnormal orofacial morphology MP:0003744
img facial cleft MP:0008797
img taut facial appearance MP:0000437
img abnormal paranasal sinus morphology MP:0002240
img abnormal snout morphology MP:0000443
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img craniofacial phenotype MP:00053825img abnormal head morphology MP:0000432
Genes (477)

Species:
human : 477
Page Size
Current 25
  Page 1 of 20
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanCOMMD3-BMI1100532731
INFERRED
HumanLHX8431707LIM homeobox 8
INFERRED
HumanOR8A1390275olfactory receptor, family 8, subfamily A, member 1
INFERRED
HumanFEZF1389549FEZ family zinc finger 1
INFERRED
HumanMIA3375056melanoma inhibitory activity family, member 3
INFERRED
HumanHCN1348980hyperpolarization activated cyclic nucleotide-gated potassium channel 1
INFERRED
HumanTBX10347853T-box 10
INFERRED
HumanACSM4341392acyl-CoA synthetase medium-chain family member 4
INFERRED
HumanRSPO2340419R-spondin 2
INFERRED
HumanSH3PXD2B285590SH3 and PX domains 2B
INFERRED
HumanOR10A4283297olfactory receptor, family 10, subfamily A, member 4
INFERRED
HumanSP8221833Sp8 transcription factor
INFERRED
HumanGSX2170825GS homeobox 2
INFERRED
HumanMDGA2161357MAM domain containing glycosylphosphatidylinositol anchor 2
INFERRED
HumanNKX2-3159296
INFERRED
HumanFREM1158326FRAS1 related extracellular matrix 1
INFERRED
HumanNXNL2158046nucleoredoxin-like 2
INFERRED
HumanRDH10157506retinol dehydrogenase 10 (all-trans)
INFERRED
HumanGSC145258goosecoid homeobox
INFERRED
HumanTRPM6140803transient receptor potential cation channel, subfamily M, member 6
Click here to display 92 evidence detail records.
HumanSLC32A1140679solute carrier family 32 (GABA vesicular transporter), member 1
INFERRED
HumanTRIM71131405tripartite motif containing 71, E3 ubiquitin protein ligase
INFERRED
HumanEDARADD128178EDAR-associated death domain
INFERRED
HumanOR10J5127385olfactory receptor, family 10, subfamily J, member 5
INFERRED
HumanTTC8123016tetratricopeptide repeat domain 8
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0003743abnormal facial morphology0self