Logo arc image image
GATACA
  • Pin/Unpin Search
  • Pin/Unpin Details
Status:
Global Actions
Concepts: 0 (0)   Selected: 0 (0
Clear All Selections
 
Search
Text Search Results
Text Search Query:
none
Text Search Options:
none

Guided Help

Text Search Results
GraphTree Minimize or Maximize this Category
 Disease: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Anatomy: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 Gene: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Jax Mouse Phenotype: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Human Phenotype: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Gene Ontology: Biological Processes: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Gene Ontology: Cellular Component: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Gene Ontology: Molecular Function: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 Pathway: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Drug: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 Genomic Expression Atlas --
      Microarray Datasets: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 PubMed: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 CoExpression Atlas: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 CoExpression: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 Interactions: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Details
Link-It Detail - Human Phenotype - Abnormality of the musculature of the upper limbs
Debug Stats
  • ### Total Build Time: 25 ms 32.486 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 224 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_DEFINITION gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 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= 796 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 1.495 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=1 ms Completed: 1 ms rowSize= 4.931 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=23 ms Completed: 23 ms rowSize= 23.877 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.043 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the musculature of the upper limbs HP:0001446
Parents (2)
img Abnormality of the musculature of the limbs HP:0009127
img Abnormality of the upper limb HP:0002817
Children (4)
img Abnormality of the shoulder girdle musculature HP:0001435
img Abnormality of the musculature of the upper arm HP:0001457
img Abnormality of the musculature of the hand HP:0001421
img Aplasia/Hypoplasia involving the musculature of the upper limbs HP:0001467
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of the musculature of the limbs HP:0009127
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of the musculature of the limbs HP:0009127
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of the musculature of the limbs HP:0009127
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of the upper limb HP:0002817
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of the upper limb HP:0002817
Genes (60)

Species:
human : 60
Page Size
Current 25
  Page 1 of 3
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanSPG38100049707spastic paraplegia 38 (autosomal dominant, Silver syndrome)
img HP RolledUp, OMIM ID: 612335
HumanDEL17Q21.31791085
img HP RolledUp, OMIM ID: 610443
HumanLOC619409619409muscular dystrophy, congenital, merosin-positive
img HP RolledUp, OMIM ID: 609456
HumanLGMD1G553991limb girdle muscular dystrophy 1G (autosomal dominant)
img HP RolledUp, OMIM ID: 609115
HumanLGMD1F404679limb girdle muscular dystrophy 1F (autosomal dominant)
img HP RolledUp, OMIM ID: 608423
HumanKANSL1284058KAT8 regulatory NSL complex subunit 1
img HP RolledUp, OMIM ID: 610443
HumanANO5203859anoctamin 5
img HP RolledUp, OMIM ID: 611307
HumanSLC52A3113278solute carrier family 52 (riboflavin transporter), member 3
img HP RolledUp, OMIM ID: 211530
HumanSLC39A1391252solute carrier family 39 (zinc transporter), member 13
img HP RolledUp, OMIM ID: 612350
HumanSPG1180208spastic paraplegia 11 (autosomal recessive)
img HP RolledUp, OMIM ID: 604360
HumanFKRP79147fukutin related protein
img HP RolledUp, OMIM ID: 607155
img HP RolledUp, OMIM ID: 606612
HumanTRPV459341transient receptor potential cation channel, subfamily V, member 4
img HP RolledUp, OMIM ID: 606071
img HP RolledUp, OMIM ID: 181405
HumanALS257679amyotrophic lateral sclerosis 2 (juvenile)
img HP RolledUp, OMIM ID: 205100
HumanSALL457167sal-like 4 (Drosophila)
img HP RolledUp, OMIM ID: 147750
img HP RolledUp, OMIM ID: 607323
HumanMDC1B53368Muscular dystrophy, congenital, 1B
img HP RolledUp, OMIM ID: 604801
HumanNSDHL50814NAD(P) dependent steroid dehydrogenase-like
img HP RolledUp, OMIM ID: 308050
HumanBSCL226580Berardinelli-Seip congenital lipodystrophy 2 (seipin)
img HP RolledUp, OMIM ID: 600794
img HP RolledUp, OMIM ID: 270685
HumanATP6V0A223545ATPase, H+ transporting, lysosomal V0 subunit a2
img HP RolledUp, OMIM ID: 278250
HumanTRIM3222954tripartite motif containing 32
img HP RolledUp, OMIM ID: 254110
HumanDNAJB610049DnaJ (Hsp40) homolog, subfamily B, member 6
img HP RolledUp, OMIM ID: 603511
HumanRBM8A9939RNA binding motif protein 8A
img HP RolledUp, OMIM ID: 274000
HumanCUL79820cullin 7
img HP RolledUp, OMIM ID: 273750
HumanMATR39782matrin 3
img HP RolledUp, OMIM ID: 606070
HumanMYOT9499myotilin
img HP RolledUp, OMIM ID: 159000
HumanLGMD1D9186limb girdle muscular dystrophy 1D (autosomal dominant)
img HP RolledUp, OMIM ID: 603511
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0001446Abnormality of the musculature of the upper limbs0self