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Symbol Name ID |
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| Synonyms | HtrA2, mnd2, OMI, Prss25 | ||||||||||||||||||
| Feature Type | protein coding gene | ||||||||||||||||||
| Genetic Map | |||||||||||||||||||
| Sequence Map |
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Vertebrate homology |
HomoloGene:113300 Vertebrate Homology Class 1 human; 1 mouse; 1 rat; 1 chimpanzee; 1 rhesus macaque; 1 cattle; 1 dog; 1 chicken; 20 zebrafish Protein SuperFamily: serine protease, HTRA type Gene Tree: Htra2 |
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| Human homologs |
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Alleles and phenotypes |
All alleles(6) :
Targeted(2)
Gene trapped(3)
Spontaneous(1)
Homozygotes for a spontaneous null mutation exhibit progressive neurological symptoms including involuntary movements, akinesis, and abnormal posture beginning at 20 days of age, striatal neurodegeneration, and lethality between 30-40 days of age. Human Diseases Modeled Using Mouse Htra2 (1) Alleles Annotated to Human Diseases(2) |
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Gene Ontology (GO) classifications |
All GO classifications: (35 annotations)
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| Expression |
cDNA source data(6) External Resources: Allen Institute GEO ArrayExpress |
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Molecular reagents |
All nucleic(8)
Genomic(1)
cDNA(7)
Microarray probesets(3) |
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Other database links |
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| Sequences |
All sequences(61) RefSeq(2) UniProt(8) |
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| Polymorphisms | RFLP(1) : SNPs(44 from dbSNP Build 128) | ||||||||||||||||||
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Protein-related information |
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| References |
(Earliest) J:12780
Jones JM, et al., mnd2: a new mouse model of inherited motor neuron disease. Genomics. 1993 Jun;16(3):669-77 (Latest) J:186355 Li B, et al., Omi/HtrA2 is a positive regulator of autophagy that facilitates the degradation of mutant proteins involved in neurodegenerative diseases. Cell Death Differ. 2010 Nov;17(11):1773-84 All references(65) |
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Other accession IDs |
MGD-MRK-12335, MGI:2141430, MGI:97039 |
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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