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Symbol Name ID |
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| Synonyms | bHLHb37 | ||||||||||||||||||
| Feature Type | protein coding gene | ||||||||||||||||||
| Genetic Map | |||||||||||||||||||
| Sequence Map |
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Vertebrate homology |
HomoloGene:23779 Vertebrate Homology Class 1 human; 1 mouse; 1 rat; 1 chimpanzee; 1 rhesus macaque; 1 cattle; 1 dog Gene Tree: Hes7 |
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| Human homologs |
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Alleles and phenotypes |
All alleles(7) :
Targeted(7)
Homozygotes for a targeted null mutation exhibit disrupted somite formation leading to skeletal defects including short trunk and tail, reduced numbers of ribs, and deformed and fused vertebrae, and neonatal death. Some heterozygotes have tail kinks. |
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Gene Ontology (GO) classifications |
All GO classifications: (18 annotations)
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| Expression |
Literature Summary: (45 records) Data Summary: Results (160) Tissues (145) Images (7) Theiler Stages: 15, 17, 19, 21, 22, 23, 28
External Resources: Allen Institute GEO ArrayExpress |
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Molecular reagents |
All nucleic(13)
cDNA(11)
Primer pair(2)
Microarray probesets(2) |
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Other database links |
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| Sequences |
All sequences(17) RefSeq(2) UniProt(1) |
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| Polymorphisms | SNPs(10 from dbSNP Build 128) | ||||||||||||||||||
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Protein-related information |
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| References |
(Earliest) J:68229
Bessho Y, et al., Hes7: a bHLH-type repressor gene regulated by Notch and expressed in the presomitic mesoderm. Genes Cells. 2001 Feb;6(2):175-85 (Latest) J:186213 Sparrow DB, et al., A mechanism for gene-environment interaction in the etiology of congenital scoliosis. Cell. 2012 Apr 13;149(2):295-306 All references(72) |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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Citing These Resources Funding Information Warranty Disclaimer & Copyright Notice Send questions and comments to User Support. |
last database update 05/08/2013 MGI 5.13 |
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