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Details
Link-It Detail - Jax Mouse Phenotype - abnormal head morphology
Debug Stats
  • ### Total Build Time: 277 ms 21.847 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 376 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 271 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 176 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= 587 bytes
  • CONCEPT_CHILDREN gt=6 ms Completed: 6 ms rowSize= 2.351 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=269 ms Completed: 269 ms rowSize= 15.236 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.162 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal head morphology MP:0000432
Definition (1)
any structural anomaly of the portion of the body containing the brain and organs of sight, hearing, taste, and smell
Synonyms (1)
"head abnormalities" BROAD
Parents (1)
img abnormal craniofacial morphology MP:0000428
Children (5)
img abnormal head size MP:0011496
img abnormal outer ear morphology MP:0002177
img abnormal head shape MP:0011495
img acephaly MP:0009579
img abnormal facial morphology MP:0003743
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img craniofacial phenotype MP:00053824img abnormal craniofacial morphology MP:0000428
Genes (592)

Species:
human : 592
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanCOMMD3-BMI1100532731
INFERRED
HumanGPR89A653519G protein-coupled receptor 89A
INFERRED
HumanCISD2493856CDGSH iron sulfur domain 2
INFERRED
HumanLHX8431707LIM homeobox 8
INFERRED
HumanOR8A1390275olfactory receptor, family 8, subfamily A, member 1
INFERRED
HumanFEZF1389549FEZ family zinc finger 1
INFERRED
HumanBLOC1S3388552biogenesis of lysosomal organelles complex-1, subunit 3
INFERRED
HumanMIA3375056melanoma inhibitory activity family, member 3
INFERRED
HumanHCN1348980hyperpolarization activated cyclic nucleotide-gated potassium channel 1
INFERRED
HumanTBX10347853T-box 10
INFERRED
HumanFREM2341640FRAS1 related extracellular matrix protein 2
Click here to display 108 evidence detail records.
HumanACSM4341392acyl-CoA synthetase medium-chain family member 4
INFERRED
HumanRSPO2340419R-spondin 2
INFERRED
HumanSH3PXD2B285590SH3 and PX domains 2B
INFERRED
HumanSLC24A5283652solute carrier family 24 (sodium/potassium/calcium exchanger), member 5
INFERRED
HumanOR10A4283297olfactory receptor, family 10, subfamily A, member 4
INFERRED
HumanASPM259266asp (abnormal spindle) homolog, microcephaly associated (Drosophila)
INFERRED
HumanSP8221833Sp8 transcription factor
INFERRED
HumanGSX1219409GS homeobox 1
INFERRED
HumanGSX2170825GS homeobox 2
INFERRED
HumanSPRED1161742sprouty-related, EVH1 domain containing 1
INFERRED
HumanMDGA2161357MAM domain containing glycosylphosphatidylinositol anchor 2
INFERRED
HumanNKX2-3159296
INFERRED
HumanFREM1158326FRAS1 related extracellular matrix 1
INFERRED
HumanNXNL2158046nucleoredoxin-like 2
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0000432abnormal head morphology0self