RecName: Full=Rab GTPase-activating protein 1; AltName: Full=GAP and c - Protein

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Biallelic loss-of-function variants in RABGAP1 cause a novel neurodevelopmental syndrome. [Genet Med. 2022]
Biallelic loss-of-function variants in RABGAP1 cause a novel neurodevelopmental syndrome.
Oh RY, Deshwar AR, Marwaha A, Sabha N, Tropak M, Hou H, Yuki KE, Wilson MD, Rump P, Lunsing R, et al. Genet Med. 2022 Nov; 24(11):2399-2407. Epub 2022 Sep 9.
Genetic determinants of micronucleus formation in vivo. [Nature. 2024]
Genetic determinants of micronucleus formation in vivo.
Adams DJ, Barlas B, McIntyre RE, Salguero I, van der Weyden L, Barros A, Vicente JR, Karimpour N, Haider A, Ranzani M, et al. Nature. 2024 Mar; 627(8002):130-136. Epub 2024 Feb 14.
Neuron-specific protein network mapping of autism risk genes identifies shared biological mechanisms and disease-relevant pathologies. [Cell Rep. 2022]
Neuron-specific protein network mapping of autism risk genes identifies shared biological mechanisms and disease-relevant pathologies.
Murtaza N, Cheng AA, Brown CO, Meka DP, Hong S, Uy JA, El-Hajjar J, Pipko N, Unda BK, Schwanke B, et al. Cell Rep. 2022 Nov 22; 41(8):111678.

RefSeq protein isoforms
See 8 reference sequence protein isoforms for the Rabgap1 gene.

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Mouse Genome Informatics (MGI) [Mouse Genome Informatics (MGI)]
Mouse Genome Informatics (MGI)
Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System
Reactome [Reactome]
Reactome
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

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Protein