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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:7824 Vertebrate Homology Class 1 human; 1 mouse; 1 rat; 1 chimpanzee; 1 rhesus macaque; 1 cattle; 1 dog; 1 zebrafish Gene Tree: Mab21l2 |
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| Human homologs |
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Alleles and phenotypes |
All alleles(1) :
Targeted(1)
Homozygous mutation of this gene results in omphalocele and defects in ventral body wall formation resulting in death at mid-gestation. Mutants have impaired development of the retina and lens. |
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Gene Ontology (GO) classifications |
All GO classifications: (6 annotations)
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| Expression |
Literature Summary: (8 records) Data Summary: Results (143) Tissues (111) Images (22) Theiler Stages: 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24
External Resources: Allen Institute GEO ArrayExpress |
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Molecular reagents |
All nucleic(44)
Genomic(1)
cDNA(42)
Other(1)
Microarray probesets(3) |
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Other database links |
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| Sequences |
All sequences(18) RefSeq(2) UniProt(1) |
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| Polymorphisms | RFLP(1) : SNPs(10 from dbSNP Build 128) | ||||||||||||||||||
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Protein-related information |
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| References |
(Earliest) J:57575
Wong RL, et al., Genomic cloning and chromosomal localization of the mouse Mab21l2 locus. Cytogenet Cell Genet. 1999;86(1):21-4 (Latest) J:186931 Saito Y, et al., Mab21l2 is essential for embryonic heart and liver development. PLoS One. 2012;7(3):e32991 All references(29) |
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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