Symbol Name ID |
Lrrc51
leucine rich repeat containing 51 MGI:1916608 |
Darker colors indicate more annotations |
Human Phenotypes | Abnormal fundus morphology |
Disease(s) Associated with LRTOMT | |
autosomal recessive nonsyndromic deafness 63 |
Mouse Phenotypes | abnormal retina blood vessel morphology |
abnormal retina morphology |
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Availability | Mouse Genotype | ||
Lrrc51tm1b(EUCOMM)Hmgu/Lrrc51tm1b(EUCOMM)Hmgu |
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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