About   Help   FAQ
Symbol
Name
ID
Vps13b
vacuolar protein sorting 13B
MGI:1916380
Phenotype annotations related to skeleton
Darker colors indicate more annotations
Human Phenotypes
Micrognathia
Hypoplasia of the maxilla
Hypoplasia of the zygomatic bone
Microcephaly
Genu valgum
Clinodactyly of the 5th finger
Arachnodactyly
Tapered finger
Sandal gap
Slender toe
Finger syndactyly
Short metatarsal
Short metacarpal
Cubitus valgus
Joint hypermobility
Abnormal hip bone morphology
Pectus excavatum
Thoracic scoliosis
Lumbar hyperlordosis
Kyphosis
Scoliosis
Disease(s) Associated with VPS13B
Cohen syndrome


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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
04/30/2024
MGI 6.23
The Jackson Laboratory