Gene table: search width pubmed_id = 15034582


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Disease phenotype
Item
in
this
table
Key
references
Gene symbol (chromosome)

protein
All allelic disease phenotypes - locus/disease symbols
Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia 1 - (AD)
5.35
15034582
16247064
VCP (9p13-p12)
Valosin-containing protein
* Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 1 - IBMPFD1
* Inclusion body myopathy with early-onset paget disease and frontotemporal dement - IBMPFD
* Amyotrophic lateral sclerosis 14, with or without frontotemporal dementia - ALS14
* Scapuloperoneal muscular dystrophy and dropped head syndrome
* Charcot-Marie-Tooth neuropathy Type 2Y - CMT2Y