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RGD Search Result

2472 records found for search term Lmna

GENES
17 Found    View Genes for All Species
         Rattus norvegicus   2     View Rat Genes Report
         Mus musculus   3     View Mouse Genes Report
         Homo sapiens   4     View Human Genes Report
         Chinchilla lanigera   2     View Chinchilla Genes Report
         Pan paniscus   2     View Bonobo Genes Report
         Canis lupus familiaris   2     View Dog Genes Report
         Ictidomys tridecemlineatus   2     View Squirrel Genes Report

SSLPS
1 Found   
         Homo sapiens   1     View Human SSLPs Report

REFERENCES
83 Found    View References for All Species

CELL LINES
20 Found    View Cell Lines for All Species

VARIANTS
2351 Found    View Variants for All Species

  
Result Matrix
  Rat Mouse Hum Chin Bono Dog Squ
Genes: 2 3 4 2 2 2 2
QTLs: 0 0 0 0 0 0 0
Strains: 0 0 0 0 0 0 0
SSLPs: 0 0 1 0 0 0 0
Promoters: 0 0 0 0 0 0 0
Cell Lines: 0 3 17 0 0 0 0
Variants: 0 0 2351 0 0 0 0

Ontologies

Curators at RGD make annotations to genes, QTLs and strains using standardized vocabularies/ontologies. Your search returned annotations to the terms below.

ChEBI: ChEBI Ontology
term browser Dibenzo[h,rst]pentaphene

EFO: Experimental Factor Ontology
term browser AG11498
term browser AG11513
term browser Charcot-Marie-Tooth disease type 2B1
term browser congenital muscular dystrophy due to LMNA mutation
term browser dilated cardiomyopathy
term browser dilated cardiomyopathy 1A
term browser Emery-Dreifuss muscular dystrophy 2, autosomal dominant
term browser Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
term browser level of muscular LMNA-interacting protein (human) in cerebrospinal fluid
term browser level of muscular LMNA-interacting protein in blood serum
term browser LMNA-related cardiocutaneous progeria syndrome
term browser mandibuloacral dysplasia with type A lipodystrophy
term browser muscular LMNA-interacting protein
term browser muscular LMNA-interacting protein (human)

HP: Human Phenotype
term browser Abnormal muscle fiber lamin A/C
term browser Anti-lamin A antibody positivity

OBA: Ontology of Biological Attributes
term browser level of muscular LMNA-interacting protein in blood serum

RDO: RGD Disease Ontology
term browser autosomal dominant Emery-Dreifuss muscular dystrophy 2
term browser Autosomal Emery-Dreifuss Muscular Dystrophy
term browser autosomal recessive Emery-Dreifuss muscular dystrophy 3
term browser Charcot-Marie-Tooth disease type 2B1
term browser congenital muscular dystrophy due to LMNA mutation
term browser dilated cardiomyopathy 1A
term browser dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome
term browser familial partial lipodystrophy type 2
term browser Laminopathies
term browser lipofibromatosis-like neural tumor
term browser mandibuloacral dysplasia type A lipodystrophy
term browser progeria
term browser restrictive dermopathy 2