138 phenotypes from 7 alleles in 6 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Ror2em1(IMPC)Mbp/Ror2+ C57BL/6N-Ror2em1(IMPC)Mbp/MbpMmucd	abnormal retina vasculature morphology	J:211773
	abnormal vitreous body morphology	J:211773
	cataract	J:211773
	persistence of hyaloid vascular system	J:211773
Ror2em1(IMPC)Mbp/Ror2em1(IMPC)Mbp C57BL/6N-Ror2em1(IMPC)Mbp/MbpMmucd	abnormal craniofacial morphology	J:211773
	abnormal limb morphology	J:211773
	abnormal placenta morphology	J:211773
	abnormal placenta vasculature	J:211773
	abnormal tail morphology	J:211773
	cleft palate	J:211773
	embryonic growth retardation	J:211773
	polydactyly	J:211773
	preweaning lethality, complete penetrance	J:211773
Ror2tm1.2Meg/Ror2tm1.2Meg involves: 129S4/SvJae * C57BL/6 * FVB/N	abnormal facial morphology	J:182150
	caudal body truncation	J:182150
	short limbs	J:182150
Ror2tm1Anec/Ror2+ B6.129S1-Ror2tm1Anec	normal limbs/digits/tail phenotype	J:134490
Ror2tm1Anec/Ror2tm1Anec B6.129S1-Ror2tm1Anec	abnormal axial skeleton morphology	J:134490
	abnormal bone mineralization	J:134490
	abnormal cartilage development	J:134490
	abnormal caudal vertebrae morphology	J:134490
	abnormal digit development	J:134490
	abnormal digit morphology	J:134490
	abnormal intervertebral disk morphology	J:134490
	abnormal limb development	J:134490
	abnormal limb morphology	J:134490
	abnormal nasal bone morphology	J:134490
	abnormal phalanx morphology	J:134490
	abnormal seminiferous tubule morphology	J:134490
	abnormal skeleton development	J:134490
	abnormal thoracic vertebrae morphology	J:134490
	abnormal vertebrae morphology	J:134490
	brachydactyly	J:134490
	brachyphalangia	J:134490
	broad nasal bone	J:134490
	caudal vertebral fusion	J:134490
	decreased body length	J:134490
	decreased body size	J:134490
	decreased bone trabecula number	J:134490
	decreased testis weight	J:134490
	decreased total body fat amount	J:134490
	decreased trabecular bone volume	J:134490
	delayed endochondral bone ossification	J:134490
	entropion	J:134490
	excessive tearing	J:134490
	normal homeostasis/metabolism phenotype	J:134490
	increased lean body mass	J:134490
	kinked tail	J:134490
	large orbits	J:134490
	oligozoospermia	J:134490
	reduced male fertility	J:134490
	rib fusion	J:134490
	short mandible	J:134490
	short metacarpal bones	J:134490
	short nasal bone	J:134490
	short snout	J:134490
	small seminiferous tubules	J:134490
	vertebral body hypoplasia	J:134490
Ror2tm1Gdy/Ror2tm1Gdy involves: 129P2/OlaHsd	abnormal caudal vertebrae morphology	J:60754
	abnormal digit development	J:134490
	abnormal endochondral bone ossification	J:60754
	abnormal femur morphology	J:60754
	abnormal fibula morphology	J:60754
	abnormal hindlimb stylopod morphology	J:134490
	abnormal humerus morphology	J:60754
	abnormal limb development	J:60754, J:134490
	abnormal long bone epiphyseal plate morphology	J:60754
	abnormal long bone epiphyseal plate proliferative zone	J:60754
	abnormal long bone morphology	J:60754
	abnormal phalanx morphology	J:60754
	abnormal radius morphology	J:60754
	abnormal skeleton development	J:134490
	abnormal tail morphology	J:60754
	abnormal tibia morphology	J:60754
	abnormal ulna morphology	J:60754
	abnormal vertebrae morphology	J:134490
	abnormal vertebral column morphology	J:60754
	brachydactyly	J:60754
	cleft palate	J:60754
	delayed endochondral bone ossification	J:60754, J:134490
	increased width of hypertrophic chondrocyte zone	J:60754
	perinatal lethality, complete penetrance	J:60754
	rib fusion	J:134490
	short femur	J:60754
	short fibula	J:60754
	short humerus	J:60754
	short limbs	J:60754
	short lumbar vertebrae	J:60754
	short nasal bone	J:134490
	short radius	J:60754
	short snout	J:60754
	short tail	J:60754
	short tibia	J:60754
	short ulna	J:60754
	small caudal vertebrae	J:60754
Ror2tm1Ymi/Ror2tm1Ymi involves: 129P2/OlaHsd	abnormal cochlear hair cell morphology	J:140886
	abnormal cochlear outer hair cell morphology	J:140886
	abnormal organ of Corti morphology	J:140886
	brachyphalangia	J:134490
Ror2tm1Ymi/Ror2tm1Ymi involves: 129P2/OlaHsd * C57BL/6	abnormal autopod morphology	J:88955
	abnormal blood homeostasis	J:60125
	abnormal cartilage development	J:60125
	abnormal cartilage morphology	J:60125
	abnormal craniofacial development	J:88955
	abnormal cranium morphology	J:88955
	abnormal forelimb stylopod morphology	J:88955
	abnormal forelimb zeugopod morphology	J:88955
	abnormal hindlimb stylopod morphology	J:88955
	abnormal hindlimb zeugopod morphology	J:88955
	abnormal jaw morphology	J:88955
	abnormal limb morphology	J:88955
	abnormal long bone epiphyseal plate proliferative zone	J:88955
	abnormal malleus morphology	J:88955
	abnormal mandible morphology	J:88955
	abnormal mandibular angle morphology	J:88955
	abnormal mandibular condyloid process morphology	J:88955
	abnormal maxilla morphology	J:88955
	abnormal Meckel's cartilage morphology	J:88955
	abnormal middle ear ossicle morphology	J:88955
	abnormal nasal capsule morphology	J:88955
	abnormal primordial germ cell migration	J:179805
	abnormal pulmonary alveolus morphology	J:60125
	abnormal rib morphology	J:60125
	abnormal sacral vertebrae morphology	J:88955
	abnormal somite development	J:88955
	abnormal somite shape	J:88955
	abnormal somite size	J:88955
	abnormal tegmen tympani morphology	J:88955
	abnormal vertebrae development	J:60125
	abnormal vertebrae morphology	J:88955
	brachydactyly	J:88955
	cleft secondary palate	J:88955
	cyanosis	J:60125
	decreased embryo size	J:60125, J:88955
	decreased length of long bones	J:88955
	decreased primordial germ cell number	J:179805
	decreased width of hypertrophic chondrocyte zone	J:88955
	delayed bone ossification	J:88955
	delayed chondrocyte differentiation	J:60125, J:88955
	failure of palatal shelf elevation	J:88955
	genital tubercle hypoplasia	J:88955
	increased cranium width	J:88955
	midface hypoplasia	J:88955
	neonatal lethality, complete penetrance	J:60125, J:88955
	ocular hypertelorism	J:88955
	perimembraneous ventricular septal defect	J:60125
	polydactyly	J:88955
	respiratory distress	J:60125
	rib fusion	J:60125
	sacral vertebral fusion	J:88955
	short mandible	J:88955
	short Meckel's cartilage	J:88955
	short metacarpal bones	J:88955
	short radius	J:88955
	short tail	J:88955
	short ulna	J:88955
	small sacral vertebrae	J:88955
	small tail bud	J:88955
	transposition of great arteries	J:60125
Ror2Tn(pb-ZG-s)1.1Mrc/Ror2Tn(pb-ZG-s)1.1Mrc involves: C57BL/6J	abnormal skeleton morphology	J:123007
	decreased birth body size	J:123007
	short limbs	J:123007
	short tail	J:123007
Ror2Y324C/Ror2Y324C involves: C57BL/6J	abnormal hindgut morphology	J:179805
	abnormal primordial germ cell migration	J:179805
	abnormal reproductive system physiology	J:179805
	abnormal tail development	J:179805
	decreased primordial germ cell number	J:179805
	impaired somite development	J:179805
	increased primordial germ cell apoptosis	J:179805
	perinatal lethality	J:179805