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Details
Link-It Detail - Jax Mouse Phenotype - abnormal head size
Debug Stats
  • ### Total Build Time: 26 ms 23.259 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 364 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 276 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=4 ms Completed: 4 ms rowSize= 579 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 1,017 bytes
  • 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=14 ms Completed: 14 ms rowSize= 18.206 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.156 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal head size MP:0011496
Definition (1)
anomaly in the average size of the portion of the body containing the brain and organs of sight, hearing, taste, and smell
Parents (1)
img abnormal head morphology MP:0000432
Children (2)
img microcephaly MP:0000433
img megacephaly MP:0000434
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img craniofacial phenotype MP:00053825img abnormal head morphology MP:0000432
Genes (73)

Species:
human : 73
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SpeciesGeneGeneIdGene NameEvidence
HumanASPM259266asp (abnormal spindle) homolog, microcephaly associated (Drosophila)
INFERRED
HumanESCO2157570establishment of sister chromatid cohesion N-acetyltransferase 2
INFERRED
HumanZIC585416Zic family member 5
INFERRED
HumanPGAP180055post-GPI attachment to proteins 1
INFERRED
HumanMCPH179648microcephalin 1
INFERRED
HumanSLC25A1960386solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19
INFERRED
HumanMESP155897mesoderm posterior 1 homolog (mouse)
INFERRED
HumanBNC254796basonuclin 2
INFERRED
HumanSOCS730837suppressor of cytokine signaling 7
INFERRED
HumanPHGDH26227phosphoglycerate dehydrogenase
INFERRED
HumanGPR12425960G protein-coupled receptor 124
INFERRED
HumanDPCD25911deleted in primary ciliary dyskinesia homolog (mouse)
INFERRED
HumanMTHFD1L25902methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1-like
INFERRED
HumanNIPBL25836Nipped-B homolog (Drosophila)
INFERRED
HumanSSBP323648single stranded DNA binding protein 3
INFERRED
HumanSATB223314SATB homeobox 2
INFERRED
HumanPDS5B23047PDS5, regulator of cohesion maintenance, homolog B (S. cerevisiae)
INFERRED
HumanDKK122943dickkopf WNT signaling pathway inhibitor 1
img Jax MP, Pubmed Id: 21228006, MOUSE PHENOTYPE ID: MGI:1298218
img Jax MP, Pubmed Id: 19620979, MOUSE PHENOTYPE ID: MGI:108028
img Jax MP, Pubmed Id: 21228006, MOUSE PHENOTYPE ID: MGI:1298218
img Jax MP, Pubmed Id: 21228006, MOUSE PHENOTYPE ID: MGI:88276
img Jax MP, Pubmed Id: 21228006, MOUSE PHENOTYPE ID: MGI:1329040
HumanPDCD1011235programmed cell death 10
INFERRED
HumanLIAS11019lipoic acid synthetase
INFERRED
HumanFRS210818fibroblast growth factor receptor substrate 2
INFERRED
HumanKLF210365Kruppel-like factor 2 (lung)
INFERRED
HumanKIF149928kinesin family member 14
INFERRED
HumanHESX18820HESX homeobox 1
INFERRED
HumanCHRD8646chordin
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0011496abnormal head size0self