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Details
Link-It Detail - Jax Mouse Phenotype - abnormal somatic motor system morphology
Debug Stats
  • ### Total Build Time: 30 ms 19.325 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 408 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 243 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 188 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=6 ms Completed: 6 ms rowSize= 597 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 598 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.588 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=18 ms Completed: 18 ms rowSize= 14.429 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.178 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal somatic motor system morphology MP:0001051
Definition (1)
any structural anomaly of the neural tissue involved in the transmission of motor signals
Synonyms (1)
"somatic motor system dysplasia" EXACT
Parents (1)
img abnormal somatic nervous system morphology MP:0002752
Children (1)
img abnormal neuromuscular synapse morphology MP:0001053
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036315img abnormal somatic nervous system morphology MP:0002752
Genes (69)

Species:
human : 69
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanSKOR2652991SKI family transcriptional corepressor 2
INFERRED
HumanAGRN375790agrin
INFERRED
HumanKY339855kyphoscoliosis peptidase
INFERRED
HumanDOK7285489docking protein 7
INFERRED
HumanFBXO45200933F-box protein 45
INFERRED
HumanLRSAM190678leucine rich repeat and sterile alpha motif containing 1
INFERRED
HumanNKX6-284504
INFERRED
HumanDNAJC580331DnaJ (Hsp40) homolog, subfamily C, member 5
INFERRED
HumanISL264843ISL LIM homeobox 2
INFERRED
HumanSLC5A760482solute carrier family 5 (sodium/choline cotransporter), member 7
INFERRED
HumanALS257679amyotrophic lateral sclerosis 2 (juvenile)
INFERRED
HumanSCYL157410SCY1-like 1 (S. cerevisiae)
INFERRED
HumanCLIP325999CAP-GLY domain containing linker protein 3
INFERRED
HumanSYNE123345spectrin repeat containing, nuclear envelope 1
INFERRED
HumanMYCBP223077MYC binding protein 2, E3 ubiquitin protein ligase
INFERRED
HumanRER111079RER1 retention in endoplasmic reticulum 1 homolog (S. cerevisiae)
INFERRED
HumanAFG3L210939AFG3 ATPase family member 3-like 2 (S. cerevisiae)
INFERRED
HumanNES10763nestin
INFERRED
HumanBASP110409brain abundant, membrane attached signal protein 1
INFERRED
HumanCACNG210369calcium channel, voltage-dependent, gamma subunit 2
INFERRED
HumanGPHN10243gephyrin
INFERRED
HumanECEL19427endothelin converting enzyme-like 1
INFERRED
HumanCACNA2D29254calcium channel, voltage-dependent, alpha 2/delta subunit 2
INFERRED
HumanSLC6A59152solute carrier family 6 (neurotransmitter transporter), member 5
INFERRED
HumanMADD8567MAP-kinase activating death domain
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0001051abnormal somatic motor system morphology0self