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Details
Link-It Detail - Jax Mouse Phenotype - abnormal artery morphology
Debug Stats
  • ### Total Build Time: 184 ms 24.188 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 380 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 234 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
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  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 587 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 4.644 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.585 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=182 ms Completed: 182 ms rowSize= 15.306 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.164 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal artery morphology MP:0002191
Definition (1)
any structural anomaly of the blood vessels that carry blood away from the heart
Synonyms (1)
"arterial dysplasia" EXACT
Parents (1)
img abnormal blood vessel morphology MP:0001614
Children (10)
img abnormal coronary artery morphology MP:0004111
img abnormal artery development MP:0003410
img abnormal systemic artery morphology MP:0011655
img calcified artery MP:0006133
img abnormal pulmonary trunk morphology MP:0000486
img arteriosclerosis MP:0003991
img abnormal pulmonary artery morphology MP:0000484
img abnormal arteriole morphology MP:0004112
img artery occlusion MP:0006134
img artery stenosis MP:0006135
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img cardiovascular system phenotype MP:00053855img abnormal blood vessel morphology MP:0001614
Genes (358)

Species:
human : 358
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanCOMMD3-BMI1100532731
INFERRED
HumanSCXA100129885scleraxis homolog A (mouse)
INFERRED
HumanCCR2729230chemokine (C-C motif) receptor 2
INFERRED
HumanCFC1B653275cripto, FRL-1, cryptic family 1B
INFERRED
HumanSCXB642658scleraxis homolog B (mouse)
INFERRED
HumanGPR180160897G protein-coupled receptor 180
Click here to display 55 evidence detail records.
HumanRDH10157506retinol dehydrogenase 10 (all-trans)
INFERRED
HumanGATA5140628GATA binding protein 5
INFERRED
HumanABRA137735actin-binding Rho activating protein
INFERRED
HumanEGLN3112399egl-9 family hypoxia-inducible factor 3
INFERRED
HumanMYOCD93649myocardin
INFERRED
HumanHPS489781Hermansky-Pudlak syndrome 4
INFERRED
HumanZMYND1584225zinc finger, MYND-type containing 15
INFERRED
HumanCCM283605cerebral cavernous malformation 2
INFERRED
HumanPLVAP83483plasmalemma vesicle associated protein
INFERRED
HumanSLC2A1081031solute carrier family 2 (facilitated glucose transporter), member 10
Click here to display 55 evidence detail records.
HumanMUS8180198MUS81 structure-specific endonuclease subunit
INFERRED
HumanHPS679803Hermansky-Pudlak syndrome 6
INFERRED
HumanWNK165125WNK lysine deficient protein kinase 1
INFERRED
HumanMOSPD364598motile sperm domain containing 3
INFERRED
HumanHIF3A64344hypoxia inducible factor 3, alpha subunit
INFERRED
HumanOVOL258495ovo-like 2 (Drosophila)
INFERRED
HumanCXCL1658191chemokine (C-X-C motif) ligand 16
INFERRED
HumanNCEH157552neutral cholesterol ester hydrolase 1
INFERRED
HumanMIB157534mindbomb E3 ubiquitin protein ligase 1
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0002191abnormal artery morphology0self