Symbol Name ID |
Mthfd1
methylenetetrahydrofolate dehydrogenase (NADP+ dependent), methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthase MGI:1342005 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Abnormality of metabolism/homeostasis |
Type II diabetes mellitus |
Edema |
Hydrops fetalis |
Disease(s) Associated with MTHFD1 | ||||
developmental cardiac valvular defect | ||||
Down syndrome | ||||
neural tube defect |
Mouse Phenotypes | homeostasis/metabolism phenotype |
abnormal amino acid level |
decreased circulating serum albumin level |
abnormal enzyme/coenzyme level |
abnormal folic acid level |
abnormal nucleotide metabolism |
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Availability | Mouse Genotype | ||||||
Mthfd1Gt(XB175)Byg/Mthfd1+ | |||||||
Mthfd1tm1.1Rzn/Mthfd1+ | * | ||||||
Mthfd1tm2b(KOMP)Wtsi/Mthfd1+ |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 04/23/2024 MGI 6.23 |
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