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Symbol
Name
ID

Ror1
receptor tyrosine kinase-like orphan receptor 1
MGI:1347520

Phenotype annotations related to nervous system

Darker colors indicate more annotations

Human Phenotypes	Motor delay
Disease(s) Associated with ROR1	Motor delay
autosomal recessive nonsyndromic deafness 108

Mouse Phenotypes		abnormal axon fasciculation	abnormal cochlear hair cell morphology	abnormal sensory neuron innervation pattern	exencephaly	abnormal synapse morphology	abnormal ribbon synapse morphology	increased prepulse inhibition
Availability	Mouse Genotype	abnormal axon fasciculation	abnormal cochlear hair cell morphology	abnormal sensory neuron innervation pattern	exencephaly	abnormal synapse morphology	abnormal ribbon synapse morphology	increased prepulse inhibition
	Ror1^tm1.2Meg/Ror1^tm1.2Meg
	Ror1^tm1Ymi/Ror1^tm1Ymi
	Ror1^{em1(IMPC)Ccpcz}/Ror1⁺

Contributing Projects: 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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