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Details
Link-It Detail - Jax Mouse Phenotype - abnormal snout morphology
Debug Stats
  • ### Total Build Time: 245 ms 24.177 KB
  • CONCEPT_NAME gt=8 ms Completed: 8 ms rowSize= 378 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 264 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 184 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=6 ms Completed: 6 ms rowSize= 581 bytes
  • CONCEPT_CHILDREN gt=22 ms Completed: 22 ms rowSize= 4.080 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.570 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=199 ms Completed: 199 ms rowSize= 15.845 KB
  • CONCEPT_XREFS gt=6 ms Completed: 6 ms rowSize= 1.163 KB
  • CONCEPT_ANCILLARY gt=2 ms Completed: 2 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal snout morphology MP:0000443
Definition (1)
any structural anomaly of the anterior facial part of the face or muzzle containing the oral and nasal regions
Synonyms (1)
"snout shape abnormalities" NARROW
Parents (1)
img abnormal facial morphology MP:0003743
Children (9)
img flattened snout MP:0000447
img upturned snout MP:0006411
img pointed snout MP:0000448
img asymmetric snout MP:0008862
img broad nasal bridge MP:0000449
img long snout MP:0000446
img scaly muzzle MP:0000451
img absent snout MP:0000450
img short snout MP:0000445
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img craniofacial phenotype MP:00053826img abnormal facial morphology MP:0003743
Genes (120)

Species:
human : 120
Page Size
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanMIA3375056melanoma inhibitory activity family, member 3
INFERRED
HumanSH3PXD2B285590SH3 and PX domains 2B
INFERRED
HumanMDGA2161357MAM domain containing glycosylphosphatidylinositol anchor 2
INFERRED
HumanFREM1158326FRAS1 related extracellular matrix 1
INFERRED
HumanTRPM6140803transient receptor potential cation channel, subfamily M, member 6
INFERRED
HumanLRIG3121227leucine-rich repeats and immunoglobulin-like domains 3
INFERRED
HumanTWIST2117581twist basic helix-loop-helix transcription factor 2
Click here to display 61 evidence detail records.
HumanEGLN2112398egl-9 family hypoxia-inducible factor 2
Click here to display 61 evidence detail records.
HumanCOL27A185301collagen, type XXVII, alpha 1
INFERRED
HumanARID5B84159AT rich interactive domain 5B (MRF1-like)
Click here to display 61 evidence detail records.
HumanOPA380207optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia)
INFERRED
HumanFBXO1180204F-box protein 11
INFERRED
HumanNABP279035nucleic acid binding protein 2
Click here to display 61 evidence detail records.
HumanPRDM1663976PR domain containing 16
Click here to display 61 evidence detail records.
HumanPLEKHA159338pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1
Click here to display 61 evidence detail records.
HumanFAM20C56975family with sequence similarity 20, member C
INFERRED
HumanCHD755636chromodomain helicase DNA binding protein 7
INFERRED
HumanMKS154903Meckel syndrome, type 1
INFERRED
HumanVPS5451542vacuolar protein sorting 54 homolog (S. cerevisiae)
INFERRED
HumanLEF151176lymphoid enhancer-binding factor 1
INFERRED
HumanSCHIP129970schwannomin interacting protein 1
Click here to display 61 evidence detail records.
HumanIFT17226160intraflagellar transport 172 homolog (Chlamydomonas)
INFERRED
HumanTIPARP25976TCDD-inducible poly(ADP-ribose) polymerase
Click here to display 61 evidence detail records.
HumanNIPBL25836Nipped-B homolog (Drosophila)
INFERRED
HumanSIRT123411sirtuin 1
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0000443abnormal snout morphology0self