Not currently registered for phenotyping at IMPC
Phenotyping is currently not planned for a knockout strain of this gene.
Gene Summary
IMPC Data Collections
- No Body Weight Data
- No Embryo Imaging Data
- No Viability Data
Phenotyping is currently not planned for a knockout strain of this gene.
The analysis uses data from IMPC, along with published data on other mouse mutants, in comparison to human disease reports in OMIM, Orphanet, and DECIPHER.
Phenotype comparisons summarize the similarity of mouse phenotypes with human disease phenotypes.
The table below shows human diseases predicted to be associated to Or5an6 by phenotypic similarity.
Disease | Similarity of phenotypes |
Matching phenotypes | Source |
---|---|---|---|
Specific Language Impairment 2 | Deficit in phonologic short-term memory | OMIM:606712 | |
Specific Language Impairment 1 | Deficit in phonologic short-term memory | OMIM:606711 | |
Presenile Dementia, Kraepelin Type | Dementia | OMIM:176600 | |
7q11.23 duplication syndrome | Short attention span | DECIPHER:43 | |
Monoamine Oxidase A Deficiency | Cognitive impairment | ORPHA:3057 | |
Microangiopathy And Leukoencephalopathy, Pontine, Autosomal Dominant | Dementia, Cognitive impairment | OMIM:618564 | |
Alzheimer Disease 10 | Memory impairment, Dementia | OMIM:609636 | |
Schizophrenia 19 | Cognitive impairment | OMIM:617629 |
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