ras-specific guanine nucleotide-releasing factor RalGPS2 isoform X1 [R - Protein

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The PH-PxxP domain of RalGPS2 promotes PC12 cells differentiation acting as a dominant negative for RalA GTPase activation. [Neurosci Res. 2010]
The PH-PxxP domain of RalGPS2 promotes PC12 cells differentiation acting as a dominant negative for RalA GTPase activation.
Ceriani M, Amigoni L, Scandiuzzi C, Berruti G, Martegani E. Neurosci Res. 2010 Mar; 66(3):290-8. Epub 2009 Dec 16.
Identification and characterization of a new family of guanine nucleotide exchange factors for the ras-related GTPase Ral. [J Biol Chem. 2000]
Identification and characterization of a new family of guanine nucleotide exchange factors for the ras-related GTPase Ral.
Rebhun JF, Chen H, Quilliam LA. J Biol Chem. 2000 May 5; 275(18):13406-10.
Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium. [Brief Bioinform. 2011]
Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium.
Gaudet P, Livstone MS, Lewis SE, Thomas PD. Brief Bioinform. 2011 Sep; 12(5):449-62. Epub 2011 Aug 27.

RefSeq mRNA
See reference mRNA sequence for the Ralgps2 gene (XM_039090755.2).
RefSeq protein isoforms
See 18 reference sequence protein isoforms for the Ralgps2 gene.

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ras-specific guanine nucleotide-releasing factor RalGPS2 isoform X1 [Rattus norv...
ras-specific guanine nucleotide-releasing factor RalGPS2 isoform X1 [Rattus norvegicus]
gi|1958672484|ref|XP_038946683.1|

Protein
Dysautonomia, Familial
Dysautonomia, Familial
An autosomal disorder of the peripheral and autonomic nervous systems limited to individuals of Ashkenazic Jewish descent. Clinical manifestations are present at birth and inc...<br/>Year introduced: 1981

MeSH
Myotonic Dystrophy
Myotonic Dystrophy
Neuromuscular disorder characterized by PROGRESSIVE MUSCULAR ATROPHY; MYOTONIA, and various multisystem atrophies. Mild INTELLECTUAL DISABILITY may also occur. Abnormal TRINUC...<br/>Year introduced: 2000(1966)

MeSH
Refsum Disease
Refsum Disease
An autosomal recessive familial disorder that usually presents in childhood with POLYNEUROPATHY; SENSORINEURAL HEARING LOSS; ICHTHYOSIS; ATAXIA; RETINITIS PIGMENTOSA; and CARD...<br/>Year introduced: 1996 (1964)

MeSH

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Protein