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Protein-coding gene in the species Homo sapiens
DEPDC5 (or DEP domain-containing 5) is a human protein of poorly understood function but has been associated with cancer in several studies. It is encoded
DEPDC5
Failure of certain neurons to migrate during brain development
mutations associated with FCD2a and FCD 2b include MTOR, PI3KCA, AKT3, and DEPDC5. Mutations in these genes lead to enhanced mTOR pathway signaling at critical
Focal_cortical_dysplasia
Protein complex
at least two highly conserved complexes: the "GATOR1" complex containing DEPDC5, NPRL2 and NPRL3 and the ""GATOR2" complex containing Mios, WDR24, WDR59
MTORC1
Medical condition
DEPDC5, NPRL2, NPRL3, PRIMA1, CABP4, CRH and others. In some cases, structural and genetic etiologies can coexist such as with mutations in DEPDC5. The
Sleep-related hypermotor epilepsy
Sleep-related_hypermotor_epilepsy
Protein-coding gene in humans
ascribed to Nprl3 to date is as part of the GATOR1 complex (with NPRL2 and DEPDC5) that inhibits the mechanistic target of rapamycin (mTOR) kinase-complex-1
NPRL3
well as GATOR1. Additionally, C12orf66 is predicted to interact with KRAS, DEPDC5, and C7orf60. These interactions were detected by high throughput affinity
KICSTOR_subunit_2
Q5TB30 4185 DEPDC1B HGNC:24902; Q8WUY9 4186 DEPDC4 HGNC:22952; Q8N2C3 4187 DEPDC5 HGNC:18423; O75140 4188 DEPDC7 HGNC:29899; Q96QD5 4189 DEPP1 HGNC:23355;
List of human protein-coding genes 2
List_of_human_protein-coding_genes_2
DEPDC5
DEPDC5
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DEPDC5
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