Symbol Name ID |
Hcn1
hyperpolarization activated cyclic nucleotide gated potassium channel 1 MGI:1096392 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Autistic behavior |
Attention deficit hyperactivity disorder |
Disease(s) Associated with HCN1 | ||
developmental and epileptic encephalopathy 24 | ||
generalized epilepsy with febrile seizures plus 10 |
Mouse Phenotypes | behavior/neurological phenotype |
abnormal learning/memory/conditioning |
abnormal eye blink conditioning behavior |
abnormal motor learning |
decreased exploration in new environment |
abnormal spatial learning |
abnormal depression-related behavior |
increased thigmotaxis |
tremors |
abnormal locomotor behavior |
abnormal gait |
decreased locomotor activity |
abnormal pain threshold |
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Availability | Mouse Genotype | |||||||||||||
Hcn1em1(IMPC)H/Hcn1em1(IMPC)H | ||||||||||||||
Hcn1tm1.1Lex/Hcn1tm1.1Lex | ||||||||||||||
Hcn1tm2Kndl/Hcn1tm2Kndl | * | |||||||||||||
Hcn1tm1Kndl/Hcn1tm1Kndl Tg(Camk2a-cre)2Szi/? (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 04/16/2024 MGI 6.23 |
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