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Details
Link-It Detail - Jax Mouse Phenotype - abnormal frontal bone morphology
Debug Stats
  • ### Total Build Time: 161 ms 27.521 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 392 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 235 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 180 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= 1.033 KB
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 2.790 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 5.599 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=159 ms Completed: 159 ms rowSize= 15.997 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.170 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal frontal bone morphology MP:0000107
Definition (1)
any structural anomaly of the bone forming the forehead and roof of the eye orbit
Synonyms (1)
"frontal bone dysplasia" EXACT
Parents (2)
img abnormal neurocranium morphology MP:0000074
img abnormal viscerocranium morphology MP:0005274
Children (6)
img absent frontal bone MP:0004376
img small frontal bone MP:0004377
img frontal bone foramen MP:0004378
img enlarged frontal bone MP:0004375
img wide frontal bone MP:0004379
img short frontal bone MP:0004380
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img craniofacial phenotype MP:00053827img abnormal neurocranium morphology MP:0000074
img mammalian phenotype MP:0000001img skeleton phenotype MP:00053908img abnormal neurocranium morphology MP:0000074
img mammalian phenotype MP:0000001img craniofacial phenotype MP:00053827img abnormal viscerocranium morphology MP:0005274
img mammalian phenotype MP:0000001img skeleton phenotype MP:00053908img abnormal viscerocranium morphology MP:0005274
Genes (64)

Species:
human : 64
Page Size
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SpeciesGeneGeneIdGene NameEvidence
HumanGSC145258goosecoid homeobox
Click here to display 70 evidence detail records.
HumanDISP184976dispatched homolog 1 (Drosophila)
Click here to display 70 evidence detail records.
HumanARID5B84159AT rich interactive domain 5B (MRF1-like)
Click here to display 70 evidence detail records.
HumanSCUBE180274signal peptide, CUB domain, EGF-like 1
INFERRED
HumanNXN64359nucleoredoxin
INFERRED
HumanALX460529ALX homeobox 4
INFERRED
HumanPLEKHA159338pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1
Click here to display 70 evidence detail records.
HumanWDR1957728WD repeat domain 19
INFERRED
HumanHDAC855869histone deacetylase 8
INFERRED
HumanMKS154903Meckel syndrome, type 1
Click here to display 70 evidence detail records.
HumanBNC254796basonuclin 2
INFERRED
HumanANKRD1129123ankyrin repeat domain 11
INFERRED
HumanTIPARP25976TCDD-inducible poly(ADP-ribose) polymerase
Click here to display 70 evidence detail records.
HumanHECTD125831HECT domain containing E3 ubiquitin protein ligase 1
Click here to display 70 evidence detail records.
HumanSATB223314SATB homeobox 2
Click here to display 70 evidence detail records.
HumanKIF3A11127kinesin family member 3A
Click here to display 70 evidence detail records.
HumanGDF1110220growth differentiation factor 11
Click here to display 70 evidence detail records.
HumanGTF2IRD19569GTF2I repeat domain containing 1
INFERRED
HumanNOG9241noggin
Click here to display 70 evidence detail records.
HumanSGPL18879sphingosine-1-phosphate lyase 1
Click here to display 70 evidence detail records.
HumanALKBH18846alkB, alkylation repair homolog 1 (E. coli)
Click here to display 70 evidence detail records.
HumanALX18092ALX homeobox 1
INFERRED
HumanZFAND57763zinc finger, AN1-type domain 5
Click here to display 70 evidence detail records.
HumanWNT9A7483wingless-type MMTV integration site family, member 9A
Click here to display 70 evidence detail records.
HumanTGFB27042transforming growth factor, beta 2
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0000107abnormal frontal bone morphology0self