Symbol Name ID |
Lama1
laminin, alpha 1 MGI:99892 |
Darker colors indicate more annotations |
Mouse Phenotypes | abnormal retina vasculature morphology |
abnormal retina blood vessel morphology |
abnormal retina blood vessel pattern |
abnormal Muller cell morphology |
abnormal lens morphology |
persistence of hyaloid vascular system |
macrophthalmia |
abnormal ocular fundus morphology |
abnormal retina morphology |
abnormal retina inner limiting membrane morphology |
abnormal retina neuronal layer morphology |
thin retina ganglion layer |
thin retina inner nuclear layer |
thin retina inner plexiform layer |
retina outer nuclear layer degeneration |
retina spots |
abnormal vitreous body morphology |
vitreal fibroplasia |
abnormal eye electrophysiology |
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Availability | Mouse Genotype | |||||||||||||||||||
Lama1nmf223/Lama1nmf223 | ||||||||||||||||||||
Lama1nmf223/Lama1tm1.1Olf | ||||||||||||||||||||
Lama1tm2b(EUCOMM)Hmgu/Lama1+ | ||||||||||||||||||||
Lama1tm1Olf/Lama1tm1Olf Edil3Tg(Sox2-cre)1Amc/Edil3+ (conditional) |
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 09/03/2024 MGI 6.24 |
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