Symbol Name ID |
Hexb
hexosaminidase B MGI:96074 |
Darker colors indicate more annotations |
Human Phenotypes | Macroglossia |
Spasticity |
Hypotonia |
Muscle weakness |
Skeletal muscle atrophy |
Disease(s) Associated with HEXB | |||||
Sandhoff disease |
Mouse Phenotypes | muscular atrophy |
muscle hypertonia |
muscle weakness |
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Availability | Mouse Genotype | |||
Hexbtm1Grv/Hexbtm1Grv | ||||
Hexbtm1Rlp/Hexbtm1Rlp | ||||
Hexbtm1Rlp/Hexbtm1Rlp Tg(Hexb-tTA2S,tetO-Hexb)#Tjsa/0 |
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Hexbtm1Rlp/Hexbtm1Rlp Tg(SYN1-tTA2S,tetO-Hexb)#Tjsa/0 |
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 05/21/2024 MGI 6.23 |
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