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Symbol Name ID |
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| Feature Type | protein coding gene | |||||||||||||||
| Genetic Map | ||||||||||||||||
| Sequence Map |
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Vertebrate homology |
HomoloGene:68056 Vertebrate Homology Class 1 human; 1 mouse; 1 rat; 1 rhesus macaque; 1 cattle; 1 dog Protein SuperFamily: loricrin Gene Tree: Lor |
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| Human homologs |
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Alleles and phenotypes |
All alleles(2) :
Targeted(2)
Mice homozygous for disruptions in this gene are runted at birth, have a translucent skin and skin skin barrier defect. The morphological skin phenotype disappears after 4-5 days. Phenotype Images(3) |
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Gene Ontology (GO) classifications |
All GO classifications: (11 annotations)
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| Expression |
Literature Summary: (117 records) Data Summary: Results (39) Tissues (16) Images (28) Theiler Stages: 20, 21, 22, 23, 24, 25, 26, 28
External Resources: Allen Institute GEO ArrayExpress |
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Molecular reagents |
All nucleic(24)
Genomic(3)
cDNA(20)
Primer pair(1)
Microarray probesets(4) |
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Other database links |
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| Sequences |
All sequences(16) RefSeq(2) UniProt(1) |
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| Polymorphisms | RFLP(1) : SNPs(1 from dbSNP Build 128) | |||||||||||||||
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Protein-related information |
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| References |
(Earliest) J:17535
Nischt R, et al., Localization of a novel mRNA in keratinizing epithelia of the mouse: evidence for the sequential activation of differentiation-specific genes. Epithelia. 1987;1(2):165-77 (Latest) J:192592 Sotiropoulou PA, et al., BRCA1 deficiency in skin epidermis leads to selective loss of hair follicle stem cells and their progeny. Genes Dev. 2013 Jan 1;27(1):39-51 All references(151) |
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Other accession IDs |
MGD-MRK-11864, MGI:2139617, MGI:2140110 |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/08/2013 MGI 5.13 |
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