Symbol Name ID |
Hspd1
heat shock protein 1 (chaperonin) MGI:96242 |
Darker colors indicate more annotations |
Human Phenotypes | Feeding difficulties in infancy |
Urinary incontinence |
Lack of spontaneous play |
Impaired ability to form peer relationships |
Autism |
Inflexible adherence to routines |
Motor stereotypy |
Restrictive behavior |
Chest pain |
Disease(s) Associated with HSPD1 | |||||||||
autistic disorder | |||||||||
coronary artery disease | |||||||||
hereditary spastic paraplegia 13 | |||||||||
hypomyelinating leukodystrophy 4 |
Mouse Phenotypes | limb grasping |
impaired coordination |
abnormal voluntary movement |
spasticity |
abnormal vocalization |
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Availability | Mouse Genotype | |||||
Hspd1em1(IMPC)J/Hspd1+ | ||||||
Hspd1Gt(OST171441)Lex/Hspd1+ |
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 04/23/2024 MGI 6.23 |
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