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Genome Features
sorted by best match, showing 1-10 of 20
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| Score | Type | Symbol | Name | Chr | Location | Str | Best Match |
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Gene | Ids | iduronate 2-sulfatase | X | 67596244-67618259 | - | Symbol : Ids and 8 more... |
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Gene | Myo1d | myosin ID | 11 | 80295628-80593527 | - | Name : myosin ID and 1 more... |
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Gene | Atp8b2 | ATPase, class I, type 8B, member 2 | 3 | 89743403-89767430 | - | Synonym : Id and more detail... |
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Gene | Camk1d | calcium/calmodulin-dependent protein kinase ID | 2 | 5214503-5635561 | - | Name : calcium/calmodulin-dependent protein kinase ID and 1 more... |
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Gene | Idh1 | isocitrate dehydrogenase 1 (NADP+), soluble | 1 | 65205190-65225755 | - | Synonym : Id-1 and 1 more... |
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Complex/Cluster/Region | Igh | immunoglobulin heavy chain complex | 12 | 58.0 cM | Allele Synonym : iD and 1 more... | |
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Gene | Id1 | inhibitor of DNA binding 1 | 2 | 152561987-152563146 | + | Human Synonym : ID and 1 more... |
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Gene | Racgap1 | Rac GTPase-activating protein 1 | 15 | 99451708-99482052 | - | Human Synonym : ID-GAP and more detail... |
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Gene | Egr2 | early growth response 2 | 10 | 66998223-67004936 | + | Disease Ortholog : Charcot-Marie-Tooth Disease, Demyelinating, Type 1D; CMT1D and more detail... |
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Gene | Alg3 | asparagine-linked glycosylation 3 homolog (yeast, alpha-1,3-mannosyltransferase) | 16 | 20605524-20610841 | - | Disease Ortholog : Congenital Disorder of Glycosylation, Type ID; CDG1D and more detail... |
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| Vocabulary Terms sorted by best match, showing 1-8 of 8
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| Score | Term | Associated Data | Best Match |
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Disease : Mucopolysaccharidosis Type II | 1 mouse model | Synonym : Ids Deficiency |
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Protein Domain : Cytochrome c, class ID | Term : Cytochrome c, class ID | |
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Disease : Usher Syndrome, Type ID; USH1D | 3 mouse models, 1 mouse ortholog | Term : Usher Syndrome, Type ID; USH1D |
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Protein Family : mouse Id-associated protein 1 | 1 gene | Term : mouse Id-associated protein 1 |
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Disease : Congenital Disorder of Glycosylation, Type ID; CDG1D | 1 mouse ortholog | Term : Congenital Disorder of Glycosylation, Type ID; CDG1D |
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Protein Family : DNA-binding protein inhibitor, ID type | 4 genes | Term : DNA-binding protein inhibitor, ID type |
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Disease : Charcot-Marie-Tooth Disease, Demyelinating, Type 1D; CMT1D | 1 mouse ortholog | Synonym : Hmsn ID |
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Disease : Myasthenic Syndrome, Congenital, Associated with Acetylcholine Receptor Deficiency | 4 mouse models, 2 mouse orthologs | Synonym : Myasthenic Syndrome, Congenital, Type ID; CMS1D |
| Other Results By ID no results
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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 02/06/2010 MGI_4.32 Web browser compatibility |
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