Gene: Lama2 (laminin subunit alpha 2) Rattus norvegicus
Analyze
Symbol:
Lama2
Name:
laminin subunit alpha 2
Description:
Predicted to have extracellular matrix structural constituent. Involved in Schwann cell differentiation. Localizes to the basement membrane and dendritic spine. Biomarker of renovascular hypertension. Human ortholog(s) of this gene implicated in autosomal recessive limb-girdle muscular dystrophy; congenital merosin-deficient muscular dystrophy 1A; muscular dystrophy; and myopia. Orthologous to human LAMA2 (laminin subunit alpha 2); PARTICIPATES IN arrhythmogenic right ventricular cardiomyopathy pathway; cell-extracellular matrix signaling pathway; dilated cardiomyopathy pathway; INTERACTS WITH (RS)-amphetamine; 17alpha-ethynylestradiol; atrazine.
Type:
protein-coding
RefSeq Status:
MODEL
Also known as:
laminin subunit alpha-2; laminin, alpha 2; LOC309368
Orthologs:
Species
Gene symbol and name
Data Source
Assertion derived from
less info ...
Orthologs 1
Homo sapiens (human):
LAMA2 (laminin subunit alpha 2) HGNC
Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, Panther, Treefam
Mus musculus (house mouse):
Lama2 (laminin, alpha 2) HGNC
Treefam, NCBI, OMA, HomoloGene, Inparanoid, Panther, OrthoDB, Ensembl
Chinchilla lanigera (long-tailed chinchilla):
Lama2 (laminin subunit alpha 2) Transitive Ortholog Pipeline
Transitive Ortholog Pipeline
Pan paniscus (bonobo/pygmy chimpanzee):
LAMA2 (laminin subunit alpha 2) Transitive Ortholog Pipeline
Transitive Ortholog Pipeline
Canis lupus familiaris (dog):
LAMA2 (laminin subunit alpha 2) Transitive Ortholog Pipeline
Transitive Ortholog Pipeline
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):
Lama2 (laminin subunit alpha 2) Transitive Ortholog Pipeline
Transitive Ortholog Pipeline
Sus scrofa (pig):
LAMA2 (laminin subunit alpha 2) Transitive Ortholog Pipeline
Transitive Ortholog Pipeline
Other homologs 2
Homo sapiens (human):
LAMA1 (laminin subunit alpha 1) HGNC
OrthoMCL
Alliance orthologs 3
Homo sapiens (human):
LAMA2 (laminin subunit alpha 2)
Alliance
DIOPT (Ensembl Compara, HGNC, OMA, OrthoFinder, PANTHER)
Mus musculus (house mouse):
Lama2 (laminin, alpha 2)
Alliance
DIOPT (Ensembl Compara, OMA, OrthoFinder, PANTHER)
Danio rerio (zebrafish):
lama2 (laminin, alpha 2)
Alliance
DIOPT (OrthoFinder, PANTHER)
Caenorhabditis elegans (roundworm):
lam-3
Alliance
DIOPT (Ensembl Compara, OMA, OrthoFinder, PANTHER)
Drosophila melanogaster (fruit fly):
wb
Alliance
DIOPT (Ensembl Compara, OMA, PANTHER)
Allele / Splice:
Lama2Tn(sb-T2/Bart3)2.2013Mcwi
Genetic Models:
F344-Lama2Tn(sb-T2/Bart3)2.2013Mcwi
Latest Assembly:
Rnor_6.0 - RGSC Genome Assembly v6.0
Position:
Rat Assembly Chr Position (strand) Source Genome Browsers JBrowse NCBI UCSC Ensembl Rnor_6.0 1 18,491,264 - 19,143,486 (+) NCBI Rnor6.0 Rnor_6.0 rn6 Rnor6.0 Rnor_5.0 1 20,002,787 - 20,647,256 (+) NCBI Rnor5.0 Rnor_5.0 rn5 Rnor5.0 RGSC_v3.4 1 18,203,466 - 18,885,462 (+) NCBI RGSC3.4 rn4 RGSC3.4 RGSC_v3.1 1 18,324,930 - 18,885,310 (+) NCBI Celera 1 16,078,601 - 16,724,118 (+) NCBI Celera Cytogenetic Map 1 p12 NCBI
JBrowse:
View Region in Genome Browser (JBrowse)
Model
Imported Annotations - ClinVar
Autosomal Recessive Limb-Girdle Muscular Dystrophy 23 ISO RGD:1318918 8554872 ClinVar Annotator: match by term: MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 23 ClinVar PMID:25741868 Autosomal Recessive Limb-Girdle Muscular Dystrophy 23 ISO RGD:1318918 8554872 ClinVar Annotator: match by term: MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 23 ClinVar PMID:21953594 Autosomal Recessive Limb-Girdle Muscular Dystrophy 23 ISO RGD:1318918 8554872 ClinVar Annotator: match by term: MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 23 ClinVar PMID:24957499 Autosomal Recessive Limb-Girdle Muscular Dystrophy 23 ISO RGD:1318918 8554872 ClinVar Annotator: match by term: MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 23 ClinVar PMID:24957499 more ... Charcot-Marie-Tooth disease ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth disease ClinVar PMID:25648254 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Laminin alpha 2-related dystrophy ClinVar PMID:24611677 more ... congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:25741868 more ... congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:11369186 more ... congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:20207543 more ... congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:24082139 more ... congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:20207543 more ... congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Laminin alpha 2-related dystrophy ClinVar PMID:25741868 more ... congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:20207543 more ... congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:28492532 , PMID:28688748 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:20207543 more ... congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:18700894 more ... congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Laminin alpha 2-related dystrophy ClinVar PMID:24225367 , PMID:28492532 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:11287370 more ... congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:24957499 more ... congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:10611118 more ... congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:2152033 more ... congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Laminin alpha 2-related dystrophy ClinVar PMID:12552556 more ... congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:27854218 , PMID:28492532 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Laminin alpha 2-related dystrophy ClinVar PMID:23326386 , PMID:28492532 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Laminin alpha 2-related dystrophy ClinVar PMID:12552556 more ... congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:9674786 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:23911319 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:18700894 more ... congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:18700894 , PMID:25525159 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:25663498 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:9185182 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:24225367 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:24957499 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:20207543 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:18700894 , PMID:24611677 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:24534542 , PMID:27858741 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:26633542 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:16216942 , PMID:25525159 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:18700894 , PMID:25124546 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:11938437 , PMID:25214167 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:26436962 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:25663498 , PMID:28492532 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:28554332 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:25741868 , PMID:28182637 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:24611677 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:11071490 more ... congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:26304763 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:20207543 more ... congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:28182637 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:10694916 , PMID:28492532 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:28877744 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:10022829 more ... congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:25525159 , PMID:7550355 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:28688748 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:24611677 , PMID:28182637 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:27447704 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:10611118 more ... congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:25741868 more ... congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:10694916 , PMID:25525159 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Laminin alpha 2-related dystrophy ClinVar PMID:11591858 more ... congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Laminin alpha 2-related dystrophy ClinVar PMID:22426012 , PMID:28492532 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Laminin alpha 2-related dystrophy ClinVar PMID:28492532 , PMID:8957020 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Laminin alpha 2-related dystrophy ClinVar PMID:1061118 more ... congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Congenital Muscular Dystrophy, LAMA2-related ClinVar PMID:29706646 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Laminin alpha 2-related dystrophy ClinVar PMID:12552556 more ... congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:11938437 more ... congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Laminin alpha 2-related dystrophy ClinVar PMID:25741868 more ... congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:18414213 more ... congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:12552556 more ... congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:12552556 more ... congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:12552556 more ... congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:12601554 more ... congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Laminin alpha 2-related dystrophy ClinVar PMID:18700894 , PMID:28492532 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:11071490 more ... congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Laminin alpha 2-related dystrophy ClinVar PMID:20207543 , PMID:28492532 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:17949279 more ... congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:24225367 , PMID:25741868 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:25741868 , PMID:27353517 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by OMIM:607855 ClinVar PMID:26104111 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:18700894 more ... congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:25741868 , PMID:26467025 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:11369186 more ... congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Laminin alpha 2-related dystrophy ClinVar PMID:18414213 more ... congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Laminin alpha 2-related dystrophy ClinVar PMID:20207543 more ... congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:12100448 more ... congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Congenital Muscular Dystrophy, LAMA2-related ClinVar PMID:18414213 , PMID:25741868 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:12552556 more ... congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:25741868 , PMID:9674786 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by OMIM:607855 ClinVar PMID:16216942 , PMID:9541105 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by OMIM:607855 ClinVar PMID:18700894 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by OMIM:607855 ClinVar PMID:11591858 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by OMIM:607855 ClinVar congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Congenital Muscular Dystrophy, LAMA2-related ClinVar PMID:25741868 more ... congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by OMIM:607855 ClinVar PMID:24033266 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by OMIM:607855 ClinVar PMID:22675738 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:18700894 , PMID:25741868 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:25663498 , PMID:9541105 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Congenital Muscular Dystrophy, LAMA2-related ClinVar PMID:25741868 , PMID:28492532 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Congenital Muscular Dystrophy, LAMA2-related ClinVar PMID:28492532 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by OMIM:607855 ClinVar PMID:7550355 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Merosin deficient congenital muscular dystrophy ClinVar PMID:12552556 more ... congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Congenital Muscular Dystrophy, LAMA2-related ClinVar PMID:25741868 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by OMIM:607855 ClinVar PMID:16216942 congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Laminin alpha 2-related dystrophy ClinVar PMID:21953594 more ... congenital merosin-deficient muscular dystrophy 1A ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Laminin alpha 2-related dystrophy ClinVar PMID:26467025 , PMID:28492532 congenital muscular dystrophy ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Congenital muscular dystrophy ClinVar congenital muscular dystrophy ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Congenital muscular dystrophy ClinVar PMID:25741868 congenital muscular dystrophy ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Congenital muscular dystrophy ClinVar PMID:24082139 more ... congenital muscular dystrophy ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Congenital muscular dystrophy ClinVar PMID:25741868 more ... congenital muscular dystrophy ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Congenital muscular dystrophy ClinVar PMID:27854218 , PMID:28492532 congenital muscular dystrophy ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Congenital muscular dystrophy ClinVar PMID:26633542 congenital muscular dystrophy ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Congenital muscular dystrophy ClinVar PMID:10611118 more ... congenital muscular dystrophy ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Congenital muscular dystrophy ClinVar PMID:25741868 more ... congenital muscular dystrophy ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Muscular dystrophy, congenital ClinVar PMID:25741868 , PMID:28492532 congenital muscular dystrophy ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Congenital muscular dystrophy ClinVar PMID:28492532 Congenital Muscular Dystrophy due to Partial LAMA2 Deficiency ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Congenital muscular dystrophy due to partial LAMA2 deficiency ClinVar Congenital Muscular Dystrophy due to Partial LAMA2 Deficiency ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Congenital muscular dystrophy due to partial LAMA2 deficiency ClinVar PMID:22166137 more ... Congenital Muscular Dystrophy due to Partial LAMA2 Deficiency ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Congenital muscular dystrophy due to partial LAMA2 deficiency ClinVar PMID:11071490 more ... Congenital Muscular Dystrophy due to Partial LAMA2 Deficiency ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Congenital muscular dystrophy due to partial LAMA2 deficiency ClinVar PMID:11071490 more ... Congenital Muscular Dystrophy due to Partial LAMA2 Deficiency ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Congenital muscular dystrophy due to partial LAMA2 deficiency ClinVar PMID:25741868 Congenital Muscular Dystrophy due to Partial LAMA2 Deficiency ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Congenital muscular dystrophy due to partial LAMA2 deficiency ClinVar PMID:12552556 Congenital Muscular Dystrophy due to Partial LAMA2 Deficiency ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Congenital muscular dystrophy due to partial LAMA2 deficiency ClinVar PMID:20207543 , PMID:30301903 Congenital Muscular Dystrophy due to Partial LAMA2 Deficiency ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Congenital muscular dystrophy due to partial LAMA2 deficiency ClinVar PMID:24225367 , PMID:30055037 Congenital Muscular Dystrophy due to Partial LAMA2 Deficiency ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Congenital muscular dystrophy due to partial LAMA2 deficiency ClinVar PMID:28492532 Creatine Phosphokinase, Elevated Serum ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Elevated serum creatine phosphokinase ClinVar PMID:25741868 , PMID:9674786 Creatine Phosphokinase, Elevated Serum ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Elevated serum creatine phosphokinase ClinVar PMID:25741868 genetic disease ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Inborn genetic diseases ClinVar PMID:11938437 more ... genetic disease ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Inborn genetic diseases ClinVar PMID:12552556 more ... genetic disease ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Inborn genetic diseases ClinVar PMID:12552556 more ... genetic disease ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Inborn genetic diseases ClinVar PMID:12552556 more ... melanoma ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Malignant melanoma ClinVar Polymicrogyria ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Polymicrogyria ClinVar PMID:25741868 more ... Polymicrogyria ISO RGD:1318918 8554872 ClinVar Annotator: match by term: Polymicrogyria ClinVar PMID:29706646
Gene-Chemical Interaction Annotations
