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Symbol Name ID |
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| Synonyms | 1300010A18Rik | ||||||||||||||||||||
| Feature Type | protein coding gene | ||||||||||||||||||||
| Genetic Map | |||||||||||||||||||||
| Sequence Map |
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Vertebrate homology |
HomoloGene:3483 Vertebrate Homology Class 1 human; 1 mouse; 1 rat; 1 chimpanzee; 1 rhesus macaque; 1 cattle; 1 dog; 1 chicken; 2 zebrafish Gene Tree: Lrat |
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| Human homologs |
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Alleles and phenotypes |
All alleles(10) :
Targeted(9)
Gene trapped(1)
Mice homozygous for disruptions in this gene exhibit retinol homeostasis abnormalities and are more susceptible to vitamin A deficiency or display impaired vision associated with abnormal retinol metabolism. Males have testicular hypoplasia/atrophy and reduced mature sperm counts. |
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Gene Ontology (GO) classifications |
All GO classifications: (24 annotations)
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| Expression |
Literature Summary: (5 records) Data Summary: Results (123) Tissues (113) Images (1) Theiler Stages: 9, 11, 13, 15, 17, 20, 22, 28
External Resources: Allen Institute GEO ArrayExpress |
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Molecular reagents |
All nucleic(11)
cDNA(8)
Primer pair(3)
Microarray probesets(4) |
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Other database links |
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| Sequences |
All sequences(25) RefSeq(2) UniProt(2) |
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| Polymorphisms | SNPs(58 from dbSNP Build 128) | ||||||||||||||||||||
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Protein-related information |
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| References |
(Earliest) J:66429
Zolfaghari R, et al., Lecithin:retinol acyltransferase from mouse and rat liver. Cdna cloning and liver-specific regulation by dietary vitamin a and retinoic acid. J Lipid Res. 2000 Dec;41(12):2024-34 (Latest) J:194158 Zhang N, et al., Autosomal recessive retinitis pigmentosa E150K opsin mice exhibit photoreceptor disorganization. J Clin Invest. 2013 Jan 2;123(1):121-37 All references(70) |
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Other accession IDs |
MGI:1919009, MGI:2139712 |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 06/05/2013 MGI 5.13 |
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