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Symbol Name ID |
Mfsd2a
MFSD2 lysolipid transporter A, lysophospholipid MGI:1923824 |
| Darker colors indicate more annotations |
| Human Phenotypes | Microcephaly |
Progressive microcephaly |
Upslanted palpebral fissure |
| Disease(s) Associated with MFSD2A | |||
| primary autosomal recessive microcephaly 15 |
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 05/07/2024 MGI 6.23 |
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