ANG2 [Homo sapiens]

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VPS51 biallelic variants cause microcephaly with brain malformations: A confirmatory report. [Eur J Med Genet. 2019]
VPS51 biallelic variants cause microcephaly with brain malformations: A confirmatory report.
Uwineza A, Caberg JH, Hitayezu J, Wenric S, Mutesa L, Vial Y, Drunat S, Passemard S, Verloes A, El Ghouzzi V, et al. Eur J Med Genet. 2019 Aug; 62(8):103704. Epub 2019 Jun 14.
A neurodevelopmental disorder caused by mutations in the VPS51 subunit of the GARP and EARP complexes. [Hum Mol Genet. 2019]
A neurodevelopmental disorder caused by mutations in the VPS51 subunit of the GARP and EARP complexes.
Gershlick DC, Ishida M, Jones JR, Bellomo A, Bonifacino JS, Everman DB. Hum Mol Genet. 2019 May 1; 28(9):1548-1560.
Soluble fms-like tyrosine kinase-1 and angiotensin2 target calcitonin gene-related peptide family peptides in maternal vascular smooth muscle cells in pregnancy†. [Biol Reprod. 2021]
Soluble fms-like tyrosine kinase-1 and angiotensin2 target calcitonin gene-related peptide family peptides in maternal vascular smooth muscle cells in pregnancy†.
Chauhan M, Betancourt A, Balakrishnan M, Mishra A, Fox K, Belfort M, Yallampalli C. Biol Reprod. 2021 May 7; 104(5):1071-1083.

RefSeq protein
See the reference protein sequence for vacuolar protein sorting-associated protein 51 homolog (NP_037397.2).

Nucleotide
Nucleotide sequence from coding region
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Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

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Protein