Symbol Name ID |
Snrpb
small nuclear ribonucleoprotein B MGI:98342 |
Darker colors indicate more annotations |
Human Phenotypes | Death in infancy |
Disease(s) Associated with SNRPB | |
cerebrocostomandibular syndrome |
Mouse Phenotypes | lethality throughout fetal growth and development, incomplete penetrance |
neonatal lethality, complete penetrance |
prenatal lethality, complete penetrance |
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Availability | Mouse Genotype | |||
E2f1Tg(Wnt1-cre)2Sor/E2f1+ Snrpbem1Lajm/Snrpb+ (conditional) |
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Snrpbem1Lajm/Snrpb+ Tmem163Tg(ACTB-cre)2Mrt/Tmem163+ (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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