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Cell lines sorted after organ of phenotypic resemblance.
Cell lines sorted after biological source for establishment.
Cell lines sorted after the cell line category according to Cellosaurus.
Cell lines sorted on descending RNA expression.
Cell lines sorted alphabetically.
GENE INFORMATION
Gene name
TBC1D7 (HGNC Symbol)
Synonyms
dJ257A7.3, FLJ32666
Description
TBC1 domain family, member 7 (HGNC Symbol)
Entrez gene summary
This gene encodes a member of the TBC-domain containing protein family. The encoded protein functions as a subunit of the tuberous sclerosis TSC1-TSC2 complex which plays a role in the regulation of cellular growth and differentiation. Mutations in this gene have been associated with autosomal recessive megalencephaly. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2013]
Q9P0N9 [Direct mapping] TBC1 domain family member 7 A0A024R011 [Target identity:100%; Query identity:100%] TBC1 domain family, member 7, isoform CRA_a
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MEMSAT3 predicted membrane proteins SPOCTOPUS predicted membrane proteins THUMBUP predicted membrane proteins Predicted intracellular proteins Disease related genes Protein evidence (Kim et al 2014) Protein evidence (Ezkurdia et al 2014)
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GO:0005096 [GTPase activator activity] GO:0005515 [protein binding] GO:0016023 [cytoplasmic membrane-bounded vesicle] GO:0017137 [Rab GTPase binding] GO:0031398 [positive regulation of protein ubiquitination] GO:0031410 [cytoplasmic vesicle] GO:0032007 [negative regulation of TOR signaling] GO:0036064 [ciliary basal body] GO:0070848 [response to growth factor] GO:0090630 [activation of GTPase activity] GO:1902018 [negative regulation of cilium assembly]
