vcp Gene Set

Dataset GeneRIF Biological Term Annotations
Category structural or functional annotations
Type biological term
Description valosin containing protein|The protein encoded by this gene is a member of a family that includes putative ATP-binding proteins involved in vesicle transport and fusion, 26S proteasome function, and assembly of peroxisomes. This protein, as a structural protein, is associated with clathrin, and heat-shock protein Hsc70, to form a complex. It has been implicated in a number of cellular events that are regulated during mitosis, including homotypic membrane fusion, spindle pole body function, and ubiquitin-dependent protein degradation. [provided by RefSeq, Jul 2008] (NCBI Entrez Gene Database, 7415)
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Genes

29 genes co-occuring with the biological term vcp in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Symbol Name
AKT1 v-akt murine thymoma viral oncogene homolog 1
ASPSCR1 alveolar soft part sarcoma chromosome region, candidate 1
CAPN3 calpain 3, (p94)
CAV1 caveolin 1, caveolae protein, 22kDa
CFTR cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
EGF epidermal growth factor
ELF2 E74-like factor 2 (ets domain transcription factor)
EPSTI1 epithelial stromal interaction 1 (breast)
IL4 interleukin 4
IL6 interleukin 6
KLF8 Kruppel-like factor 8
MAPT microtubule-associated protein tau
MIR129-1 microRNA 129-1
MIR129-2 microRNA 129-2
NF1 neurofibromin 1
NPLOC4 nuclear protein localization 4 homolog (S. cerevisiae)
PBX1 pre-B-cell leukemia homeobox 1
PBX2 pre-B-cell leukemia homeobox 2
PTPRO protein tyrosine phosphatase, receptor type, O
RELA v-rel avian reticuloendotheliosis viral oncogene homolog A
SH2D1A SH2 domain containing 1A
SQSTM1 sequestosome 1
TARDBP TAR DNA binding protein
TNF tumor necrosis factor
UBXN6 UBX domain protein 6
UFD1L ubiquitin fusion degradation 1 like (yeast)
VCP valosin containing protein
VCPKMT valosin containing protein lysine (K) methyltransferase
WRN Werner syndrome, RecQ helicase-like