Gene: Pomgnt1 (protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase) Mus musculus
Analyze
Symbol:
Pomgnt1
Name:
protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase
Description:
Predicted to have beta-1,3-galactosyl-O-glycosyl-glycoprotein beta-1,3-N-acetylglucosaminyltransferase activity and manganese ion binding activity. Involved in protein O-linked glycosylation. Predicted to localize to the integral component of Golgi membrane. Used to study Walker-Warburg syndrome and muscular dystrophy-dystroglycanopathy. Human ortholog(s) of this gene implicated in lissencephaly; muscular dystrophy (multiple); and retinitis pigmentosa. Is expressed in several structures, including alimentary system; genitourinary system; liver; nervous system; and respiratory system. Orthologous to human POMGNT1 (protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)); PARTICIPATES IN O-linked glycan biosynthetic pathway; INTERACTS WITH 17alpha-ethynylestradiol; 2,3,7,8-tetrachlorodibenzodioxine; 2,3,7,8-Tetrachlorodibenzofuran.
Type:
protein-coding
RefSeq Status:
VALIDATED
Also known as:
0610016I07Rik; 4930467B06Rik; O-mannosyl N-acetylglucosaminyltransferase; protein O-linked mannose beta1,2-N-acetylglucosaminyltransferase; protein O-linked-mannose beta-1,2-N-acetylglucosaminyltransferase 1; RP23-319H15.3
Orthologs:
Species
Gene symbol and name
Data Source
Assertion derived from
less info ...
Orthologs 1
Homo sapiens (human):
POMGNT1 (protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)) HGNC
EggNOG, Ensembl, HGNC, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, PhylomeDB, Treefam
Rattus norvegicus (Norway rat):
Pomgnt1 (protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)) HGNC
Treefam, EggNOG, OrthoMCL, NCBI, OMA, HomoloGene, Inparanoid, Panther, PhylomeDB, OrthoDB, Ensembl
Chinchilla lanigera (long-tailed chinchilla):
Pomgnt1 (protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)) Transitive Ortholog Pipeline
Transitive Ortholog Pipeline
Pan paniscus (bonobo/pygmy chimpanzee):
POMGNT1 (protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)) Transitive Ortholog Pipeline
Transitive Ortholog Pipeline
Canis lupus familiaris (dog):
POMGNT1 (protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)) Transitive Ortholog Pipeline
Transitive Ortholog Pipeline
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):
Pomgnt1 (protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)) Transitive Ortholog Pipeline
Transitive Ortholog Pipeline
Sus scrofa (pig):
POMGNT1 (protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)) Transitive Ortholog Pipeline
Transitive Ortholog Pipeline
Alliance orthologs 3
Rattus norvegicus (Norway rat):
Pomgnt1 (protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-))
Alliance
DIOPT (Hieranoid, InParanoid, OMA, OrthoFinder, OrthoInspector, PANTHER, PhylomeDB, TreeFam)
Homo sapiens (human):
POMGNT1 (protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-))
Alliance
DIOPT (HGNC, Hieranoid, InParanoid, OMA, OrthoFinder, OrthoInspector, PANTHER, PhylomeDB, Roundup, TreeFam)
Danio rerio (zebrafish):
pomgnt1 (protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-))
Alliance
DIOPT (Hieranoid, OMA, OrthoFinder, OrthoInspector, PANTHER, PhylomeDB, Roundup, TreeFam, ZFIN)
Latest Assembly:
GRCm38 - Mouse Genome Assembly GRCm38
Position:
Mouse Assembly Chr Position (strand) Source Genome Browsers JBrowse NCBI UCSC Ensembl GRCm38 Ensembl 4 116,123,840 - 116,159,849 (+) Ensembl GRCm38 4 116,150,498 - 116,159,844 (+) NCBI GRCm38 GRCm38 mm10 GRCm38 MGSCv37 4 115,823,123 - 115,832,449 (+) NCBI GRCm37 mm9 NCBIm37 MGSCv36 4 115,648,457 - 115,657,776 (+) NCBI mm8 Celera 4 114,888,693 - 114,898,002 (+) NCBI Celera Cytogenetic Map 4 D1 NCBI
JBrowse:
View Region in Genome Browser (JBrowse)
Model
Disease Annotations
RGD Manual Annotations
Gliosis IMP 11532765 RGD lissencephaly ISO RGD:1601994 11065022 DNA:frameshift mutations, missense mutations, deletion:exon, intron:multiple RGD muscular dystrophy ISO RGD:1601994 1599152 DNA:missense mutations, nonsense mutation, snp:exons, intron:multiple (human) RGD Walker-Warburg syndrome ISO RGD:1601994 11532772 DNA:missense mutations, nonsense mutation: :multiple RGD Walker-Warburg syndrome ISO RGD:1601994 11065512 DNA:deletions, splice-site mutation:exon, intron:multiple RGD Walker-Warburg syndrome ISO RGD:1601994 1554293 DNA:missense mutations, splice-site mutations, deletions: :multiple RGD Walker-Warburg syndrome ISO RGD:1601994 11071487 DNA:missense mutations:exon:p.R265H (935G>A), p.R311Q (1037G>A), p.C442R (1465C>T) (human) RGD
Imported Annotations - ClinVar
autosomal recessive limb-girdle muscular dystrophy ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Limb-Girdle Muscular Dystrophy, Recessive ClinVar PMID:25741868 , PMID:28492532 autosomal recessive limb-girdle muscular dystrophy ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Limb-Girdle Muscular Dystrophy, Recessive ClinVar PMID:15466003 more ... autosomal recessive limb-girdle muscular dystrophy ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Limb-Girdle Muscular Dystrophy, Recessive ClinVar PMID:25326635 more ... autosomal recessive limb-girdle muscular dystrophy ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Limb-Girdle Muscular Dystrophy, Recessive ClinVar PMID:24033266 more ... autosomal recessive limb-girdle muscular dystrophy ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Limb-Girdle Muscular Dystrophy, Recessive ClinVar PMID:15466003 more ... autosomal recessive limb-girdle muscular dystrophy ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Limb-Girdle Muscular Dystrophy, Recessive ClinVar PMID:28492532 autosomal recessive limb-girdle muscular dystrophy ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Limb-Girdle Muscular Dystrophy, Recessive ClinVar autosomal recessive limb-girdle muscular dystrophy ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Limb-Girdle Muscular Dystrophy, Recessive ClinVar PMID:25741868 more ... autosomal recessive limb-girdle muscular dystrophy ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Limb-Girdle Muscular Dystrophy, Recessive ClinVar PMID:25741868 autosomal recessive limb-girdle muscular dystrophy type 2O ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Limb-girdle muscular dystrophy-dystroglycanopathy, type C3 ClinVar PMID:17878207 more ... autosomal recessive limb-girdle muscular dystrophy type 2O ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Limb-girdle muscular dystrophy-dystroglycanopathy, type C3 ClinVar PMID:17906881 more ... autosomal recessive limb-girdle muscular dystrophy type 2O ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Limb-girdle muscular dystrophy-dystroglycanopathy, type C3 ClinVar PMID:19299310 more ... autosomal recessive limb-girdle muscular dystrophy type 2O ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Limb-girdle muscular dystrophy-dystroglycanopathy, type C3 ClinVar PMID:15466003 more ... autosomal recessive limb-girdle muscular dystrophy type 2O ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Limb-girdle muscular dystrophy-dystroglycanopathy, type C3 ClinVar PMID:15466003 more ... autosomal recessive limb-girdle muscular dystrophy type 2O ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Limb-girdle muscular dystrophy-dystroglycanopathy, type C3 ClinVar PMID:17878207 more ... autosomal recessive limb-girdle muscular dystrophy type 2O ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Limb-girdle muscular dystrophy-dystroglycanopathy, type C3 ClinVar PMID:28492532 , PMID:28688748 autosomal recessive limb-girdle muscular dystrophy type 2O ISO RGD:1601994 8554872 ClinVar Annotator: match by term: MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, POMGNT1-RELATED ClinVar PMID:15466003 more ... autosomal recessive limb-girdle muscular dystrophy type 2O ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Limb-girdle muscular dystrophy-dystroglycanopathy, type C3 ClinVar PMID:15236414 more ... autosomal recessive limb-girdle muscular dystrophy type 2O ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Limb-girdle muscular dystrophy-dystroglycanopathy, type C3 ClinVar PMID:17030669 , PMID:22554691 autosomal recessive limb-girdle muscular dystrophy type 2O ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Limb-girdle muscular dystrophy-dystroglycanopathy, type C3 ClinVar PMID:19299310 more ... autosomal recessive limb-girdle muscular dystrophy type 2O ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Limb-girdle muscular dystrophy-dystroglycanopathy, type C3 ClinVar autosomal recessive limb-girdle muscular dystrophy type 2O ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Limb-girdle muscular dystrophy-dystroglycanopathy, type C3 ClinVar PMID:17559086 more ... autosomal recessive limb-girdle muscular dystrophy type 2O ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Limb-girdle muscular dystrophy-dystroglycanopathy, type C3 ClinVar PMID:11709191 more ... autosomal recessive limb-girdle muscular dystrophy type 2O ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Limb-girdle muscular dystrophy-dystroglycanopathy, type C3 ClinVar PMID:25326635 more ... autosomal recessive limb-girdle muscular dystrophy type 2O ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Limb-girdle muscular dystrophy-dystroglycanopathy, type C3 ClinVar PMID:25741868 autosomal recessive limb-girdle muscular dystrophy type 2O ISO RGD:1601994 8554872 ClinVar Annotator: match by term: MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, POMGNT1-RELATED ClinVar PMID:11709191 more ... autosomal recessive limb-girdle muscular dystrophy type 2O ISO RGD:1601994 8554872 ClinVar Annotator: match by term: MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, POMGNT1-RELATED ClinVar PMID:17878207 more ... autosomal recessive limb-girdle muscular dystrophy type 2O ISO RGD:1601994 8554872 ClinVar Annotator: match by OMIM:613157 ClinVar PMID:22419172 autosomal recessive limb-girdle muscular dystrophy type 2O ISO RGD:1601994 8554872 ClinVar Annotator: match by term: MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, POMGNT1-RELATED ClinVar PMID:25741868 more ... autosomal recessive limb-girdle muscular dystrophy type 2O ISO RGD:1601994 8554872 ClinVar Annotator: match by term: MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, POMGNT1-RELATED ClinVar PMID:25741868 , PMID:28492532 autosomal recessive limb-girdle muscular dystrophy type 2O ISO RGD:1601994 8554872 ClinVar Annotator: match by term: MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, POMGNT1-RELATED ClinVar PMID:28492532 Charcot-Marie-Tooth disease dominant intermediate C ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Charcot-Marie-Tooth disease, dominant intermediate C ClinVar PMID:28492532 congenital muscular dystrophy ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Congenital muscular dystrophy ClinVar PMID:17878207 more ... congenital muscular dystrophy ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Congenital Muscular Dystrophy, alpha-dystroglycan related ClinVar PMID:15466003 more ... congenital muscular dystrophy ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Congenital muscular dystrophy ClinVar PMID:15236414 more ... congenital muscular dystrophy ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Congenital muscular dystrophy ClinVar PMID:25326635 more ... congenital muscular dystrophy ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Congenital muscular dystrophy ClinVar PMID:28492532 congenital muscular dystrophy ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Congenital Muscular Dystrophy, alpha-dystroglycan related ClinVar PMID:15466003 more ... congenital muscular dystrophy ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Congenital Muscular Dystrophy, alpha-dystroglycan related ClinVar PMID:24033266 more ... congenital muscular dystrophy ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Congenital muscular dystrophy ClinVar congenital muscular dystrophy ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Congenital muscular dystrophy ClinVar PMID:25741868 congenital muscular dystrophy ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Muscular dystrophy, congenital ClinVar PMID:25741868 , PMID:28492532 congenital muscular dystrophy ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Muscular dystrophy, congenital ClinVar PMID:25741868 more ... congenital muscular dystrophy-dystroglycanopathy type A ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Congenital muscular alpha-dystroglycanopathy with brain and eye anomalies ClinVar PMID:11709191 more ... congenital muscular dystrophy-dystroglycanopathy type A3 ISO RGD:1601994 8554872 ClinVar Annotator: match by term: WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMGNT1-RELATED ClinVar PMID:19299310 more ... congenital muscular dystrophy-dystroglycanopathy type A3 ISO RGD:1601994 8554872 ClinVar Annotator: match by term: WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMGNT1-RELATED ClinVar PMID:15466003 more ... congenital muscular dystrophy-dystroglycanopathy type A3 ISO RGD:1601994 8554872 ClinVar Annotator: match by term: WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMGNT1-RELATED ClinVar PMID:17030669 , PMID:22554691 congenital muscular dystrophy-dystroglycanopathy type A3 ISO RGD:1601994 8554872 ClinVar Annotator: match by term: WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMGNT1-RELATED ClinVar congenital muscular dystrophy-dystroglycanopathy type A3 ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A3 ClinVar PMID:12588800 more ... congenital muscular dystrophy-dystroglycanopathy type A3 ISO RGD:1601994 8554872 ClinVar Annotator: match by term: WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMGNT1-RELATED ClinVar PMID:15466003 more ... congenital muscular dystrophy-dystroglycanopathy type A3 ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A3 ClinVar PMID:15236414 more ... congenital muscular dystrophy-dystroglycanopathy type A3 ISO RGD:1601994 8554872 ClinVar Annotator: match by term: WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMGNT1-RELATED ClinVar PMID:17559086 more ... congenital muscular dystrophy-dystroglycanopathy type A3 ISO RGD:1601994 8554872 ClinVar Annotator: match by term: WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMGNT1-RELATED ClinVar PMID:15236414 more ... congenital muscular dystrophy-dystroglycanopathy type A3 ISO RGD:1601994 8554872 ClinVar Annotator: match by term: WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMGNT1-RELATED ClinVar PMID:19299310 more ... congenital muscular dystrophy-dystroglycanopathy type A3 ISO RGD:1601994 8554872 ClinVar Annotator: match by term: WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMGNT1-RELATED ClinVar PMID:11709191 more ... congenital muscular dystrophy-dystroglycanopathy type A3 ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3 ClinVar PMID:25741868 congenital muscular dystrophy-dystroglycanopathy type A3 ISO RGD:1601994 8554872 ClinVar Annotator: match by term: WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMGNT1-RELATED ClinVar PMID:15466003 more ... congenital muscular dystrophy-dystroglycanopathy type A3 ISO RGD:1601994 8554872 ClinVar Annotator: match by term: WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMGNT1-RELATED ClinVar PMID:17878207 , PMID:18195152 congenital muscular dystrophy-dystroglycanopathy type A3 ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A3 ClinVar PMID:11709191 congenital muscular dystrophy-dystroglycanopathy type A3 ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A3 ClinVar PMID:11709191 more ... genetic disease ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Inborn genetic diseases ClinVar PMID:17878207 more ... Muscular Dystrophy-Dystroglycanopathy (congenital with mental retardation), Type B, 3 ISO RGD:1601994 8554872 ClinVar Annotator: match by term: MUSCULAR DYSTROPHY, CONGENITAL, POMGNT1-RELATED ClinVar PMID:19299310 more ... Muscular Dystrophy-Dystroglycanopathy (congenital with mental retardation), Type B, 3 ISO RGD:1601994 8554872 ClinVar Annotator: match by term: MUSCULAR DYSTROPHY, CONGENITAL, POMGNT1-RELATED ClinVar PMID:15466003 more ... Muscular Dystrophy-Dystroglycanopathy (congenital with mental retardation), Type B, 3 ISO RGD:1601994 8554872 ClinVar Annotator: match by term: MUSCULAR DYSTROPHY, CONGENITAL, POMGNT1-RELATED ClinVar PMID:15236414 more ... Muscular Dystrophy-Dystroglycanopathy (congenital with mental retardation), Type B, 3 ISO RGD:1601994 8554872 ClinVar Annotator: match by term: MUSCULAR DYSTROPHY, CONGENITAL, POMGNT1-RELATED ClinVar PMID:17030669 , PMID:22554691 Muscular Dystrophy-Dystroglycanopathy (congenital with mental retardation), Type B, 3 ISO RGD:1601994 8554872 ClinVar Annotator: match by term: MUSCULAR DYSTROPHY, CONGENITAL, POMGNT1-RELATED ClinVar PMID:15466003 more ... Muscular Dystrophy-Dystroglycanopathy (congenital with mental retardation), Type B, 3 ISO RGD:1601994 8554872 ClinVar Annotator: match by term: MUSCULAR DYSTROPHY, CONGENITAL, POMGNT1-RELATED ClinVar PMID:17559086 more ... Muscular Dystrophy-Dystroglycanopathy (congenital with mental retardation), Type B, 3 ISO RGD:1601994 8554872 ClinVar Annotator: match by term: MUSCULAR DYSTROPHY, CONGENITAL, POMGNT1-RELATED ClinVar Muscular Dystrophy-Dystroglycanopathy (congenital with mental retardation), Type B, 3 ISO RGD:1601994 8554872 ClinVar Annotator: match by term: MUSCULAR DYSTROPHY, CONGENITAL, POMGNT1-RELATED ClinVar PMID:25741868 Muscular Dystrophy-Dystroglycanopathy (congenital with mental retardation), Type B, 3 ISO RGD:1601994 8554872 ClinVar Annotator: match by term: MUSCULAR DYSTROPHY, CONGENITAL, POMGNT1-RELATED ClinVar PMID:11709191 more ... Muscular Dystrophy-Dystroglycanopathy (congenital with mental retardation), Type B, 3 ISO RGD:1601994 8554872 ClinVar Annotator: match by term: MUSCULAR DYSTROPHY, CONGENITAL, POMGNT1-RELATED ClinVar PMID:17878207 , PMID:18195152 Muscular Dystrophy-Dystroglycanopathy (congenital with mental retardation), Type B, 3 ISO RGD:1601994 8554872 ClinVar Annotator: match by OMIM:613151 ClinVar PMID:19299310 more ... Retinitis Pigmentosa 76 ISO RGD:1601994 8554872 ClinVar Annotator: match by OMIM:617123 ClinVar PMID:27391550 Retinitis Pigmentosa 76 ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Retinitis pigmentosa 76 ClinVar PMID:15466003 more ... Retinitis Pigmentosa 76 ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Retinitis pigmentosa 76 ClinVar PMID:11709191 more ... Retinitis Pigmentosa 76 ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Retinitis pigmentosa 76 ClinVar PMID:19299310 more ... Retinitis Pigmentosa 76 ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Retinitis pigmentosa 76 ClinVar PMID:15466003 more ... Retinitis Pigmentosa 76 ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Retinitis pigmentosa 76 ClinVar PMID:17559086 more ... Retinitis Pigmentosa 76 ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Retinitis pigmentosa 76 ClinVar PMID:17030669 , PMID:22554691 Retinitis Pigmentosa 76 ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Retinitis pigmentosa 76 ClinVar Retinitis Pigmentosa 76 ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Retinitis pigmentosa 76 ClinVar PMID:15466003 more ... Retinitis Pigmentosa 76 ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Retinitis pigmentosa 76 ClinVar PMID:15236414 more ... Retinitis Pigmentosa 76 ISO RGD:1601994 8554872 ClinVar Annotator: match by OMIM:617123 ClinVar PMID:26908613 Retinitis Pigmentosa 76 ISO RGD:1601994 8554872 ClinVar Annotator: match by OMIM:617123 ClinVar PMID:15466003 more ... Retinitis Pigmentosa 76 ISO RGD:1601994 8554872 ClinVar Annotator: match by OMIM:617123 ClinVar PMID:12588800 more ... Walker-Warburg syndrome ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Muscle eye brain disease ClinVar PMID:17878207 more ... Walker-Warburg syndrome ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Muscle eye brain disease ClinVar PMID:15466003 more ... Walker-Warburg syndrome ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Muscle eye brain disease ClinVar PMID:15466003 more ... Walker-Warburg syndrome ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Muscle eye brain disease ClinVar PMID:17906881 more ... Walker-Warburg syndrome ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Muscle eye brain disease ClinVar PMID:19299310 more ... Walker-Warburg syndrome ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Muscle eye brain disease ClinVar PMID:15236414 more ... Walker-Warburg syndrome ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Muscle eye brain disease ClinVar PMID:15466003 more ... Walker-Warburg syndrome ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Muscle eye brain disease ClinVar PMID:17559086 more ... Walker-Warburg syndrome ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Muscle eye brain disease ClinVar PMID:15236414 more ... Walker-Warburg syndrome ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Muscle eye brain disease ClinVar PMID:11709191 more ... Walker-Warburg syndrome ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Muscle eye brain disease ClinVar PMID:28688748 Walker-Warburg syndrome ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Muscle eye brain disease ClinVar PMID:23689641 Walker-Warburg syndrome ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Muscle eye brain disease ClinVar PMID:25326635 more ... Walker-Warburg syndrome ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Muscle eye brain disease ClinVar PMID:25326635 , PMID:25741868 Walker-Warburg syndrome ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Muscle eye brain disease ClinVar PMID:28765568 Walker-Warburg syndrome ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Muscle eye brain disease ClinVar PMID:25741868 more ... Walker-Warburg syndrome ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Muscle eye brain disease ClinVar PMID:22323514 Walker-Warburg syndrome ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Muscle eye brain disease ClinVar PMID:15236414 more ... Walker-Warburg syndrome ISO RGD:1601994 8554872 ClinVar Annotator: match by term: WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMGNT1-RELATED ClinVar PMID:11709191 more ... Walker-Warburg syndrome ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Muscle eye brain disease ClinVar PMID:17878207 , PMID:18195152 Walker-Warburg syndrome ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Muscle eye brain disease ClinVar PMID:24033266 more ... Walker-Warburg syndrome ISO RGD:1601994 8554872 ClinVar Annotator: match by OMIM:253280 ClinVar PMID:19299310 more ... Walker-Warburg syndrome ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Muscle eye brain disease ClinVar PMID:25741868 , PMID:28492532 Walker-Warburg syndrome ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Muscle eye brain disease ClinVar PMID:17030669 , PMID:22554691 Walker-Warburg syndrome ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Muscle eye brain disease ClinVar PMID:17878207 more ... Walker-Warburg syndrome ISO RGD:1601994 8554872 ClinVar Annotator: match by OMIM:253280 ClinVar PMID:15466003 more ... Walker-Warburg syndrome ISO RGD:1601994 8554872 ClinVar Annotator: match by OMIM:253280 ClinVar PMID:11709191 Walker-Warburg syndrome ISO RGD:1601994 8554872 ClinVar Annotator: match by OMIM:253280 ClinVar PMID:15466003 more ... Walker-Warburg syndrome ISO RGD:1601994 8554872 ClinVar Annotator: match by OMIM:253280 ClinVar PMID:15466003 more ... Walker-Warburg syndrome ISO RGD:1601994 8554872 ClinVar Annotator: match by OMIM:253280 ClinVar PMID:12588800 , PMID:12788071 Walker-Warburg syndrome ISO RGD:1601994 8554872 ClinVar Annotator: match by OMIM:253280 ClinVar PMID:21727005 Walker-Warburg syndrome ISO RGD:1601994 8554872 ClinVar Annotator: match by OMIM:253280 ClinVar PMID:12849864 more ... Walker-Warburg syndrome ISO RGD:1601994 8554872 ClinVar Annotator: match by OMIM:253280 ClinVar PMID:17559086 Walker-Warburg syndrome ISO RGD:1601994 8554872 ClinVar Annotator: match by OMIM:253280 ClinVar Walker-Warburg syndrome ISO RGD:1601994 8554872 ClinVar Annotator: match by OMIM:253280 ClinVar PMID:17030669 Walker-Warburg syndrome ISO RGD:1601994 8554872 ClinVar Annotator: match by OMIM:253280 ClinVar PMID:21983716 Walker-Warburg syndrome ISO RGD:1601994 8554872 ClinVar Annotator: match by OMIM:253280 ClinVar PMID:19299310 , PMID:22554691 Walker-Warburg syndrome ISO RGD:1601994 8554872 ClinVar Annotator: match by OMIM:253280 ClinVar PMID:22554691 Walker-Warburg syndrome ISO RGD:1601994 8554872 ClinVar Annotator: match by OMIM:253280 ClinVar PMID:12588800 Walker-Warburg syndrome ISO RGD:1601994 8554872 ClinVar Annotator: match by OMIM:253280 ClinVar PMID:12588800 more ... Walker-Warburg syndrome ISO RGD:1601994 8554872 ClinVar Annotator: match by term: Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3 ClinVar PMID:25741868 Walker-Warburg syndrome ISO RGD:1601994 8554872 ClinVar Annotator: match by OMIM:253280 ClinVar PMID:11709191 more ... Walker-Warburg syndrome ISO RGD:1601994 8554872 ClinVar Annotator: match by OMIM:253280 ClinVar PMID:15466003 Walker-Warburg syndrome ISO RGD:1601994 8554872 ClinVar Annotator: match by OMIM:253280 ClinVar PMID:17878207 Walker-Warburg syndrome ISO RGD:1601994 8554872 ClinVar Annotator: match by OMIM:253280 ClinVar PMID:17906881
Gene-Chemical Interaction Annotations
