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Symbol
Name
ID
Vcp
valosin containing protein
MGI:99919
Phenotype annotations related to limbs/digits/tail
Darker colors indicate more annotations
Human Phenotypes
Hammertoe
Pes cavus
Ankle clonus
Limited knee flexion
Absent Achilles reflex
Distal lower limb muscle weakness
Hand muscle atrophy
Weakness of the intrinsic hand muscles
Scapular winging
Shoulder girdle muscle weakness
Proximal muscle weakness in upper limbs
Limb muscle weakness
Foot dorsiflexor weakness
Lower limb muscle weakness
Proximal muscle weakness in lower limbs
Quadriceps muscle weakness
Pelvic girdle amyotrophy
Shoulder girdle muscle atrophy
Pelvic girdle muscle weakness
Distal upper limb muscle weakness
Disease(s) Associated with VCP
Charcot-Marie-Tooth disease type 2Y
frontotemporal dementia and/or amyotrophic lateral sclerosis 6
inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1
inclusion body myositis

Mouse Phenotypes
abnormal limb bone morphology
Availability Mouse Genotype
Vcptm1Itl/Vcptm1Itl

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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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory