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Details
Link-It Detail - Jax Mouse Phenotype - abnormal xiphoid process morphology
Debug Stats
  • ### Total Build Time: 58 ms 22.202 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 398 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 212 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 183 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=2 ms Completed: 2 ms rowSize= 582 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 1.910 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.567 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=49 ms Completed: 49 ms rowSize= 16.064 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.173 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal xiphoid process morphology MP:0000159
Definition (1)
any structural anomaly of the posterior tip of the sternum
Synonyms (1)
"xyphoid process dysplasia" EXACT
Parents (1)
img abnormal sternum morphology MP:0000157
Children (4)
img split xiphoid process MP:0004678
img xiphoid process foramen MP:0004679
img absent xiphoid process MP:0011872
img small xiphoid process MP:0004680
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img skeleton phenotype MP:00053907img abnormal sternum morphology MP:0000157
Genes (47)

Species:
human : 47
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Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanKIF7374654kinesin family member 7
Click here to display 45 evidence detail records.
HumanSH3PXD2B285590SH3 and PX domains 2B
Click here to display 45 evidence detail records.
HumanTAPT1202018transmembrane anterior posterior transformation 1
INFERRED
HumanPKDCC91461protein kinase domain containing, cytoplasmic
Click here to display 45 evidence detail records.
HumanCOL27A185301collagen, type XXVII, alpha 1
INFERRED
HumanNXN64359nucleoredoxin
INFERRED
HumanVANGL257216VANGL planar cell polarity protein 2
Click here to display 45 evidence detail records.
HumanSMARCAD156916SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1
INFERRED
HumanDPPA455211developmental pluripotency associated 4
INFERRED
HumanSEMA3A10371sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A
INFERRED
HumanADAMTS29509ADAM metallopeptidase with thrombospondin type 1 motif, 2
Click here to display 45 evidence detail records.
HumanZBTB167704zinc finger and BTB domain containing 16
Click here to display 45 evidence detail records.
HumanTGFB27042transforming growth factor, beta 2
Click here to display 45 evidence detail records.
HumanZEB16935zinc finger E-box binding homeobox 1
Click here to display 45 evidence detail records.
HumanSP36670Sp3 transcription factor
Click here to display 45 evidence detail records.
HumanSOX116664SRY (sex determining region Y)-box 11
Click here to display 45 evidence detail records.
HumanSOX96662SRY (sex determining region Y)-box 9
Click here to display 45 evidence detail records.
HumanSIX16495SIX homeobox 1
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HumanRARA5914retinoic acid receptor, alpha
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HumanPRRX15396paired related homeobox 1
Click here to display 45 evidence detail records.
HumanPCSK55125proprotein convertase subtilisin/kexin type 5
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HumanLMNA4000lamin A/C
INFERRED
HumanIRF63664interferon regulatory factor 6
INFERRED
HumanIGF23481insulin-like growth factor 2 (somatomedin A)
Click here to display 45 evidence detail records.
HumanHOXC83224homeobox C8
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0000159abnormal xiphoid process morphology0self