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Symbol
Name
ID

Ror2
receptor tyrosine kinase-like orphan receptor 2
MGI:1347521

Phenotype annotations related to growth/size/body

Darker colors indicate more annotations

Human Phenotypes	Short neck	Inguinal hernia	Umbilical hernia	Short stature	Disproportionate short-limb short stature
Disease(s) Associated with ROR2
autosomal recessive Robinow syndrome

Mouse Phenotypes

abnormal nasal bone morphology

broad nasal bone

short nasal bone

abnormal nasal capsule morphology

failure of palatal shelf elevation

abnormal facial morphology

midface hypoplasia

cleft secondary palate

cleft palate

short snout

embryonic growth retardation

decreased embryo size

decreased birth body size

increased lean body mass

decreased body length

decreased body size

Availability

Mouse Genotype

Ror2^em1(IMPC)Mbp/Ror2^em1(IMPC)Mbp

Ror2^tm1.2Meg/Ror2^tm1.2Meg

Ror2^tm1Anec/Ror2^tm1Anec

Ror2^tm1Gdy/Ror2^tm1Gdy

Ror2^tm1Ymi/Ror2^tm1Ymi

Ror2^{Tn(pb-ZG-s)1.1Mrc}/Ror2^{Tn(pb-ZG-s)1.1Mrc}

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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