SYNGAP1 wt Allele
**Semantic type:** Gene or Genome
**Definition:** Human SYNGAP1 wild-type allele is located in the vicinity of 6p21.32 and is approximately 36 kb in length. This allele, which encodes Ras/Rap GTPase-activating protein SynGAP, is involved in the N-methyl-D-aspartate receptor complex signaling pathway. Mutation of the gene is associated with autosomal dominant intellectual developmental disorder 5.
**Synonyms:** - GTPase-Activating Protein, Ras, Synaptic, 135-kD, Rat, Homolog of Gene - MRD5 - RASA1 - RASA5 - Ras-GTPase-Activating Protein, Synaptic, 135-kD, Rat, Homolog of Gene - SYNGAP - SYNGAP, p135, Rat, Homolog of Gene - Synaptic Ras GTPase Activating Protein 1 Homolog (Rat) Gene - Synaptic Ras GTPase Activating Protein 1 Homolog Gene - Synaptic Ras GTPase Activating Protein 1 wt Allele - Synaptic Ras GTPase Activating Protein, 135kDa Gene - Synaptic Ras-GTPase-Activating Protein, 135-kD, Rat, Homolog of Gene
/api/v1/systems/nci_thesaurus/nodes/C190810Hierarchy Explorer
Cross-system equivalences0
No cross-system equivalences mapped for this node.