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Symbol Name ID |
Sptlc1
serine palmitoyltransferase, long chain base subunit 1 MGI:1099431 |
| Darker colors indicate more annotations |
| Human Phenotypes | Cataract |
| Disease(s) Associated with SPTLC1 | |
| hereditary sensory and autonomic neuropathy type 1A |
| Mouse Phenotypes | increased cornea thickness |
abnormal eye anterior chamber depth |
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| Availability | Mouse Genotype | ||
| Sptlc1em1(IMPC)Bay/Sptlc1+ | |||
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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