Symbol Name ID |
Hmbs
hydroxymethylbilane synthase MGI:96112 |
Darker colors indicate more annotations |
Human Phenotypes | Abdominal pain |
Urinary incontinence |
Depression |
Pain |
Chest pain |
Disease(s) Associated with HMBS | |||||
acute intermittent porphyria | |||||
sickle cell anemia |
Mouse Phenotypes | increased startle reflex |
limb grasping |
tremors |
ataxia |
impaired coordination |
jerky movement |
abnormal locomotor activation |
short stride length |
decreased locomotor activity |
hyperactivity |
motor developmental delay |
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Availability | Mouse Genotype | |||||||||||
Hmbstm1.1Rjde/Hmbstm1.1Rjde | ||||||||||||
Hmbstm1b(EUCOMM)Hmgu/Hmbs+ | ||||||||||||
Hmbstm2Uam/Hmbstm3Uam |
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 04/30/2024 MGI 6.23 |
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