rap1 GTPase-GDP dissociation stimulator 1 isoform 5 [Homo sapiens]

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Mutated RAP1GDS1 causes a new syndrome of dysmorphic feature, intellectual disability & speech delay. [Ann Clin Transl Neurol. 2020]
Mutated RAP1GDS1 causes a new syndrome of dysmorphic feature, intellectual disability & speech delay.
Asiri A, Aloyouni E, Umair M, Alyafee Y, Al Tuwaijri A, Alhamoudi KM, Almuzzaini B, Al Baz A, Alwadaani D, Nashabat M, et al. Ann Clin Transl Neurol. 2020 Jun; 7(6):956-964. Epub 2020 May 19.
Splice switching an oncogenic ratio of SmgGDS isoforms as a strategy to diminish malignancy. [Proc Natl Acad Sci U S A. 2020]
Splice switching an oncogenic ratio of SmgGDS isoforms as a strategy to diminish malignancy.
Brandt AC, McNally L, Lorimer EL, Unger B, Koehn OJ, Suazo KF, Rein L, Szabo A, Tsaih SW, Distefano MD, et al. Proc Natl Acad Sci U S A. 2020 Feb 18; 117(7):3627-3636. Epub 2020 Feb 4.
The chaperone SmgGDS-607 has a dual role, both activating and inhibiting farnesylation of small GTPases. [J Biol Chem. 2019]
The chaperone SmgGDS-607 has a dual role, both activating and inhibiting farnesylation of small GTPases.
García-Torres D, Fierke CA. J Biol Chem. 2019 Aug 2; 294(31):11793-11804. Epub 2019 Jun 13.

RefSeq mRNA
See reference mRNA sequence for the RAP1GDS1 gene (NM_001100429.2).
RefSeq protein isoforms
See 18 reference sequence protein isoforms for the RAP1GDS1 gene.

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OncoMX cancer biomarker resource [OncoMX cancer biomarker resou...]
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ExactAntigen/Labome

rap1 GTPase-GDP dissociation stimulator 1 isoform 5 [Homo sapiens]
rap1 GTPase-GDP dissociation stimulator 1 isoform 5 [Homo sapiens]
gi|155030200|ref|NP_001093899.1|

Protein
Gene Links for GEO Profiles (Select 89645133) (1)
Gene
SPTA1 spectrin alpha, erythrocytic 1 [Homo sapiens]
SPTA1 spectrin alpha, erythrocytic 1 [Homo sapiens]
Gene ID:6708

Gene
BMPR1B bone morphogenetic protein receptor type 1B [Homo sapiens]
BMPR1B bone morphogenetic protein receptor type 1B [Homo sapiens]
Gene ID:658

Gene
Gene Links for GEO Profiles (Select 89662584) (1)
Gene

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Protein