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Symbol
Name
ID
Rab23
RAB23, member RAS oncogene family
MGI:99833
Phenotype annotations related to skeleton
Darker colors indicate more annotations
Human Phenotypes
Camptodactyly
Joint contracture of the hand
Frontal bossing
Malar flattening
Micrognathia
Retrognathia
Hypoplasia of the maxilla
Brachycephaly
Cloverleaf skull
Craniosynostosis
Coronal craniosynostosis
Lambdoidal craniosynostosis
Sagittal craniosynostosis
Trigonocephaly
Oxycephaly
Large foramen magnum
Short neck
Coxa valga
Coxa vara
Broad thumb
Pseudoepiphyses of the proximal phalanges of the hand
Aplasia/Hypoplasia of the middle phalanges of the hand
Aplasia of the middle phalanx of the hand
Complete duplication of proximal phalanx of the thumb
Postaxial hand polydactyly
Clinodactyly of the 5th finger
Duplication of the proximal phalanx of the hallux
Preaxial foot polydactyly
Aplasia/Hypoplasia of the middle phalanges of the toes
Toe syndactyly
Postaxial polydactyly
Preaxial polydactyly
Brachydactyly
Cutaneous finger syndactyly
Finger syndactyly
Genu valgum
Genu varum
Metatarsus adductus
Shallow acetabular fossae
Lateral displacement of patellae
Sacral dimple
Flared iliac wings
Pectus carinatum
Pectus excavatum
Kyphoscoliosis
Scoliosis
Disease(s) Associated with RAB23
Carpenter syndrome

Mouse Phenotypes
spina bifida occulta
abnormal tarsal bone morphology
absent tibia
abnormal axial skeleton morphology
abnormal vertebral arch development
Availability Mouse Genotype
Rab23opb/Rab23opb

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
09/11/2018
MGI 6.12
The Jackson Laboratory